Illustrator Medical And Scientific Job Description Sample
Medical Illustrator - Full Time
UWorld is seeking a Medical Illustrator to create high-quality medical and scientific images for case studies and educational materials for our web-based education company. A successful candidate will have outstanding draftsmanship skills and extensive knowledge of medicine and the biological sciences.
Minimum Education Required:
- Masters degree in Medical Illustration
Minimum Experience Required:
1-3 years of medical illustration experience
Exceptional proficiency with Adobe Creative Suite (ie. Photoshop, Illustrator)
Experience working in ZBrush, UCSF Chimera, Cinema 4D, and Maya is a plus
Must be able to research and comprehend advanced scientific and medical concepts
Excellent attention to detail and organizational skills
Ability to understand direction and be receptive to feedback
Ability to work independently, as well as in collaboration
Must have confidence to work in an environment with high expectations
Job Duties: (Including but not limited to)
Design and Create (70%)
Create original illustrations for a wide range of subjects, including anatomy & physiology, surgical techniques, nursing techniques, biology, biochemistry, organic chemistry, and physics
Collaborate with our medical and science teams to create novel ways of visualizing difficult concepts
Perform work involved in executing illustrations in support of academic and test prep materials
Ensure artistic excellence and factual accuracy of the illustrated work
Consult and Collaborate (20%)
Work with team leads and designers to plan, layout, and execute the vision
Collaborate with management and team members to define schedules and deliverables, and to ensure goals are met
Help maintain an efficient and successful production process
Adapt to shifting priorities and be able to assist our on-site medical and scientific illustrators as needed
Technical/Quality Assurance (10%)
Communicate effectively with IT & quality assurance teams to anticipate and resolve issues
Work independently or in small groups to trouble-shoot and provide solutions to production issues related to creation and content building
UWorld is an equal opportunity employer of all qualified persons. The Company does not discriminate on the basis of race, color, national origin, gender, handicap or disability, or age in any of its policies, procedures, or practices in compliance with Title VI of the Civil Rights Act of 1964 (pertaining to race, color, and national origin), Section 504 of the Rehabilitation Act of 1973 (pertaining to handicap), and the Age Discrimination Act of 1975 (pertaining to age). This non-discriminatory policy covers hiring and employment at the Company.
Scientific Director, US Medical Affairs Hepatology
Oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver and interpret high-quality clinical data supporting overall product scientific and business strategy.
Key Responsibilities Include:
Manages the design and implementation of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff.
Has overall responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables.
Responsible for design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents.
May oversee the work of Associate or Assistant Scientific Directors and of Clinical Scientists working on the same or related programs.
Provides in-house clinical expertise for the molecule and disease, coordinating appropriate scientific activities with internal stakeholders as they relate to ongoing clinical projects. May participate in due diligence or other business development activity. As required by program needs, contributes in partnership with Discovery colleagues to design and implementation of translational strategies.
May serve on a Clinical Strategy Team (CST), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches.
Acts as a clinical interface and actively solicits opinion leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area.
Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Bachelors degree in the sciences; advanced degree (e.g., MS, PhD) preferred.
Ability to provide input and direction to clinical research with appropriate supervision.
At least 4 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
Ability to oversee a clinical research program of moderate complexity with minimal supervision.
Ability to perform and bring out the best in others on a cross-functional global team.
Ability to interact externally and internally to support a global scientific and business strategy.
Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
Must possess excellent oral and written English communication skills.
Medical Scientific Associate
Get ready to redefine what's possible and discover your extraordinary potential at Covance. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.
Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients—and your career.
Covance has a job opening for a Medical Scientific Associate at its clinical pharmacology facility in Madison, WI facility.
This position will ensure that each awarded project listed on the CPS Med/Scientific Project Tracker as a corresponding folder.
Additional responsibilities associated with this role:
Ensures current copies of key study documents for all assigned protocols are maintained in the Medical Monitoring files
Set up and maintain project-specific email addresses, as needed
Obtains Medical Monitor signature on required documents/forms
Support team in maintaining required study documents
Ensure that wet signature pages are obtained and filed for any applicable hard copy study documents (e.g., MRPs, subject eligibility packages, etc.)
Support Clinical Scientist in uploading required study documents to the eTMF
Enter applicable information into subject trackers (e.g., renal-impairment and hepatic-impairment trackers) and help maintain subject dosing calendar
Support team in maintaining cross-coverage schedule and training files
Help ensure each team member's training file is up to date and audit ready
Notify the team of any updated SOPs that need to be read and ensure the training files are updated accordingly
Help to set up and maintain appropriate study-specific and general training items in LearningPath
Perform other related duties as assigned
Covance believes that their best-in-class employees deserve first-class benefits. Covance offers an outstanding benefits package including medical & dental insurance, tuition reimbursement, a 401(k) plan with a generous company match, short and long-term disability, and life insurance.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.
BS degree or equivalent experience
Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access and Power Point)
- Comprehensive knowledge of GCP/ICH
- Knowledge of the clinical trial process
- 2-3 years of research experience and a BS degree (clinical experience preferred, but not required)
Scientific Director, U.S. Medical Affairs
The Scientific Director, Medical Affairs is responsible for the successful execution of Medical Affairs programs and deliverables through partnership with Medical Science Liaisons, Scientific Communications, Publications, Health Economics and Outcomes Research (HEOR), Clinical Development, and the Commercial Team.
The incumbent will be accountable, along with the Medical Affairs leadership, for high quality execution of Medical Affairs activities. The incumbent will also play a key role in the establishment and maintenance of key partnerships and collaborations, and the support of relationships with external experts, both directly, and in conjunction with, the Medical Science Liaison team.
Summary of the Essential Functions of the Job
Provide support for planning and execution of the Medical Affairs program strategy
Expertly deliver scientific and medical information and interpretation of clinical research findings.
Provide medical and scientific expertise in a cross-functional environment to field based medical science liaisons as well as internal stakeholders (Medical Affairs functions, Marketing Department, Clinical Development, Clinical Operations, Regulatory Affairs, Biostatistics, and Drug Safety/ Pharmacovigilance Department, Sales Training)
Participate in the design, conduct, analysis, and reporting of Medical Affairs led clinical trial and observational studies
Provide scientific review and expertise for independent investigator-sponsored trials (ISTs)
Support product lifecycle management activities
Plan and execute medical advisory boards.
Provide Medical expertise to the Commercial organization, including review of promotional materials, sales training, and speaker training for promotional programs
Interface with external experts and health care professionals at major medical conferences, advisory boards, and other external meetings
Maintain high level of expertise in oncology / hematology and serve as key medical resource for the oncology therapeutic area and on specific products
Provision of medical/scientific expertise for relevant marketing materials (including all promotional material) copy review in the Medical-Legal-Regulatory (MLR) Committee
Interact with the Medical Affairs function partners for activities outside of the U.S.
Develop, track, execute and report on goals and objectives.
Be accountable for compliant business practices
MD, PhD, PharmD, or equivalent
Pharmaceutical industry work experience of 2-5 years preferred
Experience as either Medical Monitor for Industry-sponsored studies or (principal or associate) Clinical Investigator in academia
Medical Affairs, Understanding of Clinical Development and Commercial activities is preferred
Ability to partner effectively with Field Medical staff is required
Solid understanding of Health Economics and Payer environment is preferred.
Strong clinical insight, understanding of translational medicine and knowledge of clinical trials, including registries, and successful prior experience in the management of an IST portfolio
Strong business acumen, vision and perspective
Ability to comprehend and combine complex sets of data
Ability to educate internal stakeholders on disease state and/or product/ brand-specific information
Ability to present and discuss complex clinical, medical, biological, or translational data
Scientific Project Director In Breast Medical Oncology
The mission of the Breast Medical Oncology Department to eliminate breast cancer reflects the core mission of The University of Texas MDAnderson Cancer Center. To accomplish our mission we have developed a functional structure focusing on patient care, clinical and translational research, and education/training for students, clinicians, staff, and the public. Our multi-pronged approach to fulfilling our mission and realizing our vision has helped to increase efficiency within the department while enhancing the quality of care our patients receive.
Salary Range 83,200-104,000- 124,800
- Ensure that strategic and tactical plans for the moonshot activities are developed and executed effectively and efficiently
o Develop and implement the business development strategies, including corporate partnerships, philanthropic, licensing and entrepreneurial opportunities
o Ensure that moonshot activities and research are aligned with strategic priorities
o Direct the ongoing development and presentation of the moonshot strategic, operating, and staffing plans, both long- and short-term, as needed to assure achievement of defined outcomes and targets
Implement, review and report on business development plans, ensuring the strategic objectives are well understood and executed by the moonshot staff
Develop and lead the business development activities in identifying, managing and implementing new collaborative opportunities with potential partners (e.g. pharmaceutical companies)
Actively engage, cultivate and manage corporate relationships to ensure efficient execution and achievement of milestones
Develop and maintain collaboration with outside stakeholders and with all staff, partners and regulatory or other official bodies (e.g. FDA)
Evaluate emerging technology, make recommendations to Director, and negotiate with producing corporations to bring or make available new technologies and services.
Develop, direct and manage the annual moonshot budget and justification of expenditures
Oversees financial management and budget related to Breast Moon Shots and the involved Platforms.
Responsible for the development and oversight of a variety of internal and external multi-year funding sources that support the moonshot.
Direct and manage all moonshot accounts and project budgets and ensure alignment with project milestones.
Develop short and long-range projections and financial plans, maintain appropriate analyses and make adjustments where appropriate.
Collaborate with a variety of staff, physicians, and faculty both internally and externally, as well as being a driver for industry collaborations
Develop metrics to measure and report upon research outcomes for experimental and/or new research initiatives
Collaborate with Regulatory and QA officials to define best practices and implement certification and compliance as applicable.
Collaborates with the leadership of the Breast Moon Shots disease site, other Moon Shots disease sites, and the Moon Shot Platforms to develop and maintain strategic business and scientific plans including schedules, project estimates, resource plans, status reports, and research protocols.
Coordinates Breast Moon Shots initiative in relation to disease site and platform areas: requires ability to coordinate and manage complex programs, multiple investigators, and interactions between Moon Shots disease site teams and Moon Shots Platform teams.
Identifies key issues, approaches, performance metrics, gap analysis, and resource needs.
Prepares quarterly progress reports, monitors, evaluates, and reports on timelines, accomplishments, planned work, budget, and provides updates as necessary.
Monitors the workflow of sample requests, assisting the participants in securing those tissues with maximum expedience by coordinating efforts with all involved parties.
Ensures effective utilization of personnel and space.
Works with Breast Moon Shot leaders, other program leaders, Platform leaders and relevant institutional infrastructure to provide data and project information in support of fundraising efforts, including but not limited to, philanthropic efforts and corporate sponsorships.
Supports the Breast Moon Shot leaders and the Platform leaders with identification, preparation, coordination, and submission/tracking of grants and manuscripts.
Facilitate interactions with Principal Investigators, faculty, staff, and study sponsors across departments, divisions, and institutional boundaries related to the Breast Moon Shots initiative.
Work with the Moon Shots Operations Team including the Chief Scientific Officer (CSO) and VP of Operations to facilitate the needs of the Breast Moon Shots projects and relationships to Platform capabilities.
Provides leadership and support for the Breast Moon Shots initiatives within all involved departments.
Assures that institutional policies and procedures are followed.
Other duties as assigned.
Master's degree. Six years experience in biotechnology/pharmaceutical/academic research or clinical research setting to include three years research program/project management experience.
With preferred degree, four years of experience in a biotechnology/pharmaceutical/academic research or clinical research setting to include one year of research program/project management experience.
MDACC experience, research involving human subjects, budgeting experience
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html
Medical Oder Scientific Advisor (M/W) Onkologie
Weltweit arbeiten die Mitarbeiter von Pfizer gemeinsam daran, die Gesundheit eines jeden Einzelnen überall zu verbessern. Während wir Arzneimittel und Medizin-Produkte entwickeln und unser Geschäft global ausweiten, halten wir jederzeit Ausschau nach neuen Talenten.
Medical oder Scientific Advisor (m/w) im Bereich Onkologie
Das erwartet Sie:
Als medizinisch-wissenschaftlicher Ansprechpartner für unsere Produkte im Bereich Onkologie sind sie verantwortlich für:
Austausch und Zusammenarbeit mit nationalen Meinungsbildnern
Entwicklung und Begleitung medizinischer Projekte
Fachliche Expertise (Medizin, Wissenschaft) in interdisziplinären Teams mit Marketing und Verkauf
Sicherstellung von medizinisch-wissenschaftlich korrekten Unterlagen in enger Zusammenarbeit mit dem Marketing
Zusammenarbeit mit Europäischen Teams
Wissenschaftliche Aus- und Fortbildung von anderen Abteilungen
Das bringen Sie mit:
Sie verfügen über ein abgeschlossenem Studium der Humanmedizin oder über ein naturwissenschaftliches Studium mit Promotion
Sie haben verfügen über klinische Erfahrung, Erfahrung im Bereich Onkologie und/oder mehrjährige Berufserfahrung in der pharmazeutischen Industrie in relevanten Bereichen.
Betriegswirtschaftliche Erfahrungen sind ein großes Plus
Zudem haben Sie Freude an zielgerichteter Kommunikation und überzeugen durch Begeisterungsfähigkeit für interdisziplinäre Fragestellungen.
Fließende deutsche und sehr gute englische Sprachkenntnisse runden Ihr Profil ab.
Wir bieten Ihnen:
… vielfältige Karriere- und Entwicklungsmöglichkeiten
… Teil eines lokalen als auch interdisziplinären Teams zu sein
… flexible Arbeitszeiten und Arbeitsorte
… umfangreiche und vielseitige Weiterbildungsmöglichkeiten
… Gesundheitsprogramme für Mitarbeiter
… die Möglichkeit, sich sozial zu engagieren
… eine offene Unternehmenskommunikation
… eine gute betriebliche Altersvorsorge
Dann freuen wir freuen uns über Ihre Online-Bewerbung mit vollständigen und aussagekräftigen Unterlagen (Lebenslauf und Anschreiben - diese und weitere Unterlagen können Sie unter "Meine Berufserfahrung" unter Ihrem Lebenslauf hinzufügen und hochladen).
Dann bewerben Sie sich noch heute auf www.pfizercareers.com.
Bitte beachten Sie, dass wir ausschließlich Bewerbung über unsere Plattform annehmen können.
Bei weiteren Fragen stehe ich Ihnen sehr gerne zur Verfügung.
Laura Brandenburg I HR Global Talent Acquisition Europe I Office +49 30 550055 52510 I mailto:firstname.lastname@example.org
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
US Medical Information Director Scientific Payer Communication
As a Medical Information professional, do you possess an understanding of US Payer, IDN and Policy Maker needs, priorities and scientific evidence requirements? Because this role directly contributes to key company goals, the MI Director of Scientific Payer Communications will need to understand how population-based decision makers are using scientific evidence to inform decisions, deploy population-management programs and cost containment strategies, and control new product coverage/use. If selected, YOU will use this knowledge to:
Influence/inform Local Medical Affairs strategic plans and activities in partnership with US Medical Affairs Leads (US MALs) and USVEO Scientists and Functional Area Leads
Identify and/or anticipate customer needs in context of brand access strategies, emerging data, or new market entrants
Assess customer evidence requirements for GSK medicines
Partner with Medical Information Scientists and Health Policy or Outcomes Experts to translate relevant evidence in a compelling and effective manner for formulary decision makers
Manage vendors and partner across a matrixed organization to ensure customer deliverables are empowering decisions based on science and related meaningful data.
Represent cross-therapeutic or product in a payer copy approval setting
Develop new and innovative ways to meet established and emerging customer needs (including leveraging technology).
Understand and assess, in the context of new product launches, the impact of changing market dynamics, unanticipated customer barriers, or evolving customer needs.
Develop a set of potential solutions that align with customer needs, product strategy and GSK compliance requirements.
Anticipate and make plans to address problems and barriers in the context of a highly matrixed and regulated environment.
Identify and discuss potential issues with commercial partners, VEO, and Health Policy partners
Problem solve solutions when current ways of working complicate or seem in conflict with our goals of meeting customer needs.
Assess risk associated with proposed medical activities/communications/customer materials will also be a key component of this role.
Work within a highly-matrixed and dynamic internal team environment.
Establish rapport, trust and credibility with individuals in highly-influential roles within US Medical Affairs or Commercial teams.
Inform, influence, and engage Director-level and higher commercial and medical business partners.
Convince or educate to understand and act on customer needs.
Manage conflict with partners in the context of challenging business situations.
Play a critical role in that alignment process by leveraging their understanding of customer needs to drive US medical strategies and priorities across multiple brands in a therapeutic area.
Be influential in determining how, and through what channels, USMA will translate and communicate evidence on GSK products to US Payers, IDNs and other formulary decision-makers.
Help inform formulary access decisions and other strategies which can have significant impact on the appropriate use of GSK products.
Serve as an equal and influential partner to Director-level and above roles in both the Medical Affairs and Commercial organizations.
Why You?Basic qualifications:
BECASE, You have:
Equivalent education or Pharm D
Previous experience in Health Outcomes, Pharmacoeconomics, Epidemiology, Health Policy/Health Services Research, Pharmacy, Public Health, Health Administration
Experience developing scientific material for US Payers or Integrated Delivery Network customers (directly or indirectly) in a communications role
Relevant scientific experience (communicating and translating scientific and firm understanding payer evidence) in a pharmaceutical, managed care, or Health System setting
Demonstrated an understanding of payer and health economic studies and ability to evaluate copy approval claims designed for a sophisticated payer and economic customer
Previous experience working with third party vendors and managing projects/budgets is required
Knowledge of US Payers, IDNs, or Government Customers (CMS, AHRQ, DERP, etc) is desired
Demonstrated customer-focus, problem solving abilities and strong conflict resolution skills
Experience influencing internal and external stakeholders on priorities and needs to fill scientific data gaps or needs of the US Payer, IDN, or Government Customer
Experience communicating and translating evidence and customer insights to/with matrix team partners; proven ability to develop innovative, customer-focused medical solutions and resources.
Proven ability to leverage technology and multiple communication channels for customer engagement.
Demonstrated ability to work in a cross-functional and matrixed team to lead or participate in organization-wide initiatives
Ability work autonomously, proactively and independently; proven ability to work across and influence a commercial and medical matrix team, both globally and locally.
Strong communication and strategic skills; demonstrated ability to identify opportunities for medical or scientific exchange of economic and payer data that is specific to the customer segments
Understanding of and ability to translate real-world evidence, CER, and other observational research studies for scientific communication needs.
Experience operating in a highly dynamic, changing, and matrixed environment
Ability to maintain a command of a large amount of scientific information across multiple therapeutic areas and show effective written/verbal communication skills
Ability to develop and maintain strong trusted relationships with internal and field based partners
Proven communication and active listening skills, professional maturity, and business acumen.
Pharm D or PhD with a MPH or MBA
Pharm.D. with additional Master's or formalized training in related health economic/health outcomes discipline is a plus
Residency and/or post-doctoral training in a pharmaceutical industry/health system/payer setting is preferred
At GSK, our mission is to improve the quality of human life by enabling people to do more, feel better and live longer. Our three world-leading businesses research and deliver innovative medicines, vaccines and consumer healthcare products. We need a talented and motivated workforce to deliver against our strategy. To achieve this, we strive to attract the best people and to create an environment that empowers and inspires.
You may apply for this position online by selecting the Apply now button.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK HR Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.
Medical And Scientific Affairs Manager
Are you a doctoral level scientist or a clinician who enjoys developing relationships with key opinion leaders? Leveraging your expertise, are you eager to travel across Europe and establish study collaboration and key opinion leader sites to develop new markets resulting in business growth? Ideally, your qualifications may include PhD, MD, MD/PhD, DVM, and/or PharmD, along with IVD clinical research experience and multi-lingual fluency.
The mission of Medical and Scientific Affairs (MASA) department at Nova Biomedical is to become the number one provider of high quality medical and scientific support through research, education, and communication.
In this senior level individual contributor role, you will develop relationships with medical and clinical laboratory key opinion leaders who will evaluate and publish papers regarding Novas new diagnostic products. This position is a key role within MASA, which is under the global strategic direction and management of the VP of MASA.
More specific responsibilities include, but are not limited to:
Contribute to establish Nova Biomedical as a leading point of care (POC) testing provider in Europe with a key focus on hospital critical care analyzers, diabetes management analyzers and handheld POC glucose, ketone, creatinine, and lactate strip testing.. This will include establishing the clinical and economic benefit in different patient care pathways (eg sepsis, trauma, AKI, diabetes, CKD, CVD).
Assist the VP of MASA in building the network of key medical and scientific opinion leaders with a strong interest in POC testing. This will include developing and improving relationships and communication with medical communities, clinical working parties, as well as key opinion leaders and other physicians and medical specialists. There is a requirement to identify from this network, evaluators for clinical (medical) studies that will clearly demonstrate the added clinical and patient value and benefit for all currently marketed and future products.
Develop, define and implement clinical protocols to achieve the medical objectives for these evaluations and clinical trials and manage and monitor the execution of all regional studies in conjunction with the VP of MASA and Director of MASA in Europe.
Ensure there is a pipeline of publications, presentations, lectures and posters based on the results of the evaluation studies. Participate in developing, preparing and presenting communication materials of study results.
Support Dealers and their Sales/Marketing Managers by establishing their and Novas scientific credibility through seminars and meetings with individual key customers.
Assist in the organization and support of local, regional, national workshops and seminars using key opinion leaders as speakers/presenters and also participate as a speaker.
Actively attend, as member when needed, scientific, medical or patient society events.
PhD in Clinical Biochemistry (or related field), MD, MD/PhD, DVM, and/or PharmD with a minimum of 5 years of relevant industry experience, including experience and/or desire to work both hands-on managing clinical studies and as a liaison in the medical community
Prior experience with Point of Care and Critical Care technologies
Prior experience in performing or managing clinical trials/evaluations
Experience in preparing scientific papers for publication in peer reviewed journals
Prior experience in presenting at meetings and giving seminars
Prior experience in developing and managing Key Opinion Leader relationships
Multi-lingual English and German is strongly preferred, French and Italian are a plus.
Ability to travel extensively throughout Europe
Manager, Medical And Scientific Affairs, New Business Opportunities, NNA US (Rockville, MD, US)
Nutricia North America, a subsidiary of Danone, is looking for Manager, Medical & Scientific Affairs, New Business Opportunities in the United States for Rockville, Maryland.
Danone is a global food company holding top positions in healthy ood through its four businesses: Fresh Dairy Products, Early Life Nutrition, Waters, and Medical Nutrition. Its mission, bringing health through food to as many people as possible, embodies commitment to human progress and business success. It gives meaning to the work of our 100,000 Danoners worldwide on an everyday basis.
For passionate people looking for autonomy and exciting career opportunities, Danone truly has something special inside.
The Manager, Medical Affairs & Scientific (MAS), New Business Opportunities is responsible for developing and implementing medical and scientific initiatives for the business unit. Lead development and execution of efficient medical/scientific affairs strategies and medical messaging, managing a strong scientific evidence generation platform and providing professional education opportunities for key stakeholders. Develop and grow effective advocacy programs driving key medical strategies and tactics aligned with brand objectives. Serve as the company's medical/scientific contact for key programs in support of corporate objectives and goals. Provide medical/ scientific support for clinical development and commercial activities.
1.Product Development/Innovation Pipeline/Evidence Generation.
Create a robust innovation and renovation product pipeline to ensure a competitive advantage in the market place.
Identify business opportunities in new therapeutic areas where nutrition solutions are a key part of medical management.
Develop and manage evidence pipeline, including prospective clinical trials and real-life evidence programs.
2.Manage key stakeholder landscape to drive business objectives.
Develop and manage key stakeholder map including health professionals, professional organizations, non-profit parent organizations and other stakeholders, including advisory boards.
Leverage relationships to drive business and awareness. Create and maintain corporate credibility and integrity.
Leverage KOLs to validate new messaging, product development and pre-market product use through early experience programs.
Maintain database of clinical evidence to support medical/marketing claims.
Responsible for maintaining competitive landscape map.
Create and manage professional advisory boards; both live and virtual.
3.Drive new product launches.
Support regulatory, marketing and medical initiatives in getting launched efficiently.
Develop medical messaging to support product safety and efficacy.
Provide medical advice to marketing, sales and research and development.
Provide expertise in the final sign off to all marketing and promotional material.
Develop communications plan with stakeholders (includes patient advocacy groups, HCPs, etc.).
Create and manage early experience programs.
4.Health care professional education (Nutricia Learning Center).
Develop education modules and product usage guidelines for HCPs.
Develop online education tools and live education events (e.g. symposia, peer-to-peer, workshops) to drive credibility, awareness and support of corporate education initiatives.
Develop online education materials, including clinical tools that support safe and effective product usage.
Access (ongoing) effectiveness of education tools through surveys and stakeholder feedback.
5.Active core member of the Therapeutic Areas team for new business opportunities.
Develop and maintain medical dashboards that align with corporate and category business objectives which drive business.
6.Manage and provide training and education to internal staff (sales and marketing).
Share knowledge and technical expertise with other team members while providing medical training to field representatives and other internal staff.
7.Other duties are assigned.
Knowledge, Skills and Abilities
Detailed knowledge of pediatric nutrition with solid clinical nutrition background.
Knowledge in basic Microsoft Office, including PowerPoint, Excel and Word. Experience using Endnotes preferred.
Clinical trial experience is highly preferred.
Strong analytical skills and experience in operational management in developing, implementing and promoting programs, projects and initiatives.
Demonstrated ability to gain staff support in a highly matrixed environment.
Strong communication skills, with an ability to clearly convey complex concepts and strategies to HCPs and other stakeholders.
Demonstrated skills and experience in problem solving, negotiations, conflict resolution, team building.
Possess strong analytical skills and business/financial acumen.
Strong negotiation skills, including an ability to collaborate well with others while possessing a "can do" attitude. Must be able to quickly establish credibility with both internal and external stakeholders.
Strong independent thinker who is willing to challenge the norm.
Inspirational leader with good people skills and ability to influence change.
Ability to deliver creative ideas for change and continuous process improvement.
Ability to network and create effective partnerships with stakeholders and colleagues.
Ability to set priorities, manage multiple projects, while effectively performing responsibilities.
Manager, Medical & Scientific Affairs, New Business Opportunities will initially not have any direct reports.
Work is conducted in an office environment.
Masters Degree or like in Nutrition or related clinical field, preferred.
Registered Dietitian required.
2 years of clinical practice experience.
Experience in clinical research design and management of clinical trials, preferred.
Experience in building interfaces between various organizations with results measured through satisfaction scores and related action plans.
Experience in creating CE-accredited HCP educational programs.
Experience in public speaking engagements.
Strategist and ability to work in a team to drive business initiatives for growth and market share.
Strong presentation skills.
Project management experience.
Strong and effective communication skills with stakeholders and across the organization, including senior management.
Willing to take chances and possibly fail.
Strong interpersonal skills and willingness to work as a team in driving success.
Change-agent: ability to challenge the norm and create new ways of thinking and driving success.
Passionate about integrity and credibility.
Nutritionally proficient with a keen understanding of customer needs.
Self-motivated and driven to succeed.
Basic understanding of business principles.
For more information about Danone, its people and its business, please visit danone.com. We have something special inside, do you?
99141. Experience: graduates
Nutricia Advanced Medical Nutrition is focused on pioneering and delivering specialized nutritional solutions and Best Care for medical professionals and their patients, helping people live healthier and longer lives. Nutricia North America was established in 1983 and is headquartered in Rockville, MD. We seek to provide solutions and services wherever nutritional intervention can be shown to improve clinical outcomes. In partnership with doctors, healthcare professionals and caregivers, we work to make a real difference in people's lives by speeding recovery and encouraging independence. Our ambition is to deliver only proven benefits through nutrition, as an integral part of disease management.
Consisting of a wide variety of FDA and Health Canada regulated nutrition products, we are especially active in the management of inherited metabolic diseases, severe pediatric allergic and gastrointestinal disorders, pediatric epilepsy, and long term and critical care for seniors.
Nutricia North America is an equal employment and affirmative action employer. All qualified applicants will receive consideration without regard to race, color, religion, disability, sex, sexual orientation, gender identity, national origin, age, physical or mental disability, veteran status, genetic characteristic or any other unlawful criterion.
Scientific Medical Writer
Writes and performs editorial work at advanced levels to ensure that all scientific/medical publications and proposals for funding are of the highest quality and contribute to the institute's reputation for academic excellence; facilitates writing and preparation of research projects; facilitates development of publications or public presentations of research results and generalized medical knowledge; develops and conducts a scientific/medical writing program for staff, residents and fellows.
Facilitates writing and preparation of research/grant proposals and applications for submission to funding agencies, maximizing potential of funding.
Works with physician groups to determine needs and researches and identifies funding sources.
Reviews agency proposal requirements, organizes and creates assignments, and ensures adherence to deadlines.
Facilitates development of print and online publications or public presentations of results from research and generalized medical knowledge by applying critical thinking to acquired scientific and medical knowledge of key disease or therapeutic areas.
Develops scientific/medical writing program for staff, residents and fellows; teaches courses on hypothesis development, data management, organizing the scientific publication, reporting guidelines and requirements for scientific literature, including research grants and clinical trials, data presentation, including figures, tables and statistics, accuracy and conciseness, authorship and ethical issues, reviewing and revising manuscripts, journals and reviewers and writing resources.
Creates and maintains databases for tracking written material and education provided.
Other duties as assigned.
Bachelor's Degree in biomedical sciences or related field required.
Master's or Doctoral Degree preferred.
Formal degree or substantial coursework in English or journalism preferred.
- None required.
Complexity of Work:
Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision.
Must be able to work in a stressful environment and take appropriate action.
- Minimum five years of scientific/medical writing experience, including research proposal development and scientific manuscript preparation.
Requires high degree of manual and finger dexterity.
Involves extensive sitting for long periods of time.
Frequent walking throughout the institution.
Involves working irregular hours.
Personal Protective Equipment:
- Follows standard precautions using personal protective equipment as required.
The policy of Cleveland Clinic and its system hospitals (Cleveland Clinic) is to provide equal opportunity to all of our employees and applicants for employment in our tobacco free and drug free environment. All offers of employment are followed by testing for controlled substance and nicotine. Job offers will be rescinded for candidates for employment who test positive for nicotine. Candidates for employment who are impacted by Cleveland Clinic's Smoking Policy will be permitted to reapply for open positions after 90 days. Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic facility.
Cleveland Clinic is pleased to be an equal employment employer: Women/Minorities/Veterans/Individuals with Disabilities
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