Illustrator Medical And Scientific Job Description Sample
UWorld is a worldwide leader in online test prep practice question banks. Since 2003, over a million students have trusted us to help them prepare for high-stakes examinations.
UWorld is seeking a talented Scientific Illustrator to join our growing illustration department. This role involves creating high-quality scientific images for our educational apps. A successful candidate will have outstanding draftsmanship skills and extensive knowledge of medicine and the biological sciences.
- Bachelor’s degree in Scientific Illustration, Biomedical Art or Pre-Medical Illustration
- 1-3 years of illustration experience preferred
- Exceptional proficiency with Adobe Creative Suite (ie. Photoshop, Illustrator)
- Experience working in ZBrush, UCSF Chimera, Cinema 4D, and Maya is a plus
Knowledge, Skills, and Abilities:
- Confidently work in an environment with high expectations
- Research and comprehend advanced scientific concepts
- Be receptive to continuous feedback from peers and management
- Have excellent attention to detail and organizational skills
- Demonstrate excellence at drawing the human figure
- Develop new skills rapidly
Design and Create
- Create original illustrations for a wide range of subjects – biology, biochemistry, general chemistry, organic chemistry, and physics
- Utilize a library of 3D and 2D assets
- Create original 3D models for illustration and animation teams
- Create illustrations according to stylistic guidelines
- Ensure artistic excellence and factual accuracy of the illustrated work
Consult and Collaborate
- Collaborate with our MCAT & College Prep teams to create novel ways of visualizing difficult concepts
- 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
- 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
Compensation and benefits:
- Paid time off (based on sliding scale according to hire date and work hours)
- Generous paid holiday schedule that includes the entire week of Christmas off
- Comprehensive benefits package (medical, vision, dental, life, disability)
- 401(k) plan for retirement with 4% employer matching (eligibility after 90 days of employment)
- On-site group fitness classes & relaxed work environment
At UWorld, we believe strength is derived from the talents, ideas, and experiences of a diverse workforce. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, veteran status, or any other protected class. UWorld is proud to be an equal opportunity employer providing a drug-free workplace. If you have a disability or special need that requires accommodation, please let us know.
To be part of the JAMA Network is to be part of our Mission to promote the science and art of medicine and the betterment of public health. Join the JAMA team as a Medical Illustrator. As part of the team, you will create accurate and effective medical and scientific illustrations and data displays for JAMA and JAMA Network print and online publications.
Responsibilities will include:
Creates original illustrations and data displays for scientific articles, Patient Pages, and Medical News in collaboration with authors and JAMA and JAMA Network editorial and production staff and authors. Evaluates submitted illustrations, data displays, and multimedia content for accuracy and suitability for publication. Completes research as necessary for conceptual development of illustrations and data displays. Coordinates activities with copyediting, graphics production, proofreading, and electronic media units.
Performs technical prepress preparation of illustrations, photos, and data displays for print and online publication.
Completes other tasks and projects as assigned, including creating and updating design elements for JAMA and JAMA Network print and online publications, and assisting with quality review of JAMA and JAMA Network print and online publications.
Master's degree in medical illustration from a medical illustration program accredited by the Council on Accreditation of Allied and Health Education Programs or Certification in Medical Illustration (CMI) from the Board of Certification of Medical Illustrators required.
Excellent drawing skills are required. Must be able to visualize spatial relationships, anatomy, and the human figure accurately.
Strong research skills required.
Previous academic and/or professional exposure to scientific concepts, including understanding of anatomy, genetics, molecular biology, and biochemistry required.
Proficiency in Adobe Creative Suite (Photoshop, Illustrator, InDesign, AfterEffects) required.
Experience in 3D modeling in MAXON Cinema 4D and Pixologic ZBrush, 3D animation, and video editing preferred.
Experience with medical journal editorial content, design, and publishing preferred.
Strong skills in typography and layout preferred.
Excellent interpersonal, oral, and written communication skills required, including demonstrated ability to collaborate with authors and editorial staff to develop illustrations.
Ability to work independently on multiple projects under tight deadlines with attention to detail required.
When applying online, include a Portfolio of your work and/or a link to view your portfolio online.
The AMA offers competitive salaries, including an incentive plan; excellent benefits and progressive technology. Our office is a business casual environment and we respect work-life balance. The American Medical Association is located at 330 N. Wabash Avenue, Chicago, IL 60611 and is convenient to all public transportation in Chicago.
We are an equal opportunity employer, committed to diversity in our workforce. All qualified applicants will receive consideration for employment. As an EOE/AA employer, the American Medical Association will not discriminate in its employment practices due to an applicant's race, color, religion, sex, age, national origin, sexual orientation, gender identity and veteran or disability status.
THE AMA IS COMMITTED TO IMPROVING THE HEALTH OF THE NATION
Senior Manager, Medical Affairs / Scientific Communications – Transcatheter Heart Valve
The Senior Manager of Scientific Communications provides comprehensive medical and scientific support to Edwards-TAVR business unit by serving as an internal expert. Develops and maintains strong scientific knowledge of the current competitive landscape and future product entries.
S/he is responsible for the development and execution of a cross-functional scientific communication strategy in full alignment with global Edwards-TAVR business strategy. Contribute to the development of the podium and publication plan that align with this strategy taking into consideration the competitive landscape and the major scientific congress calendar. Develop scientific communications in collaboration with internal stakeholders, physician investigators and KOLs to ensure maximum effectiveness in the execution of the scientific communication plan and maintenance of Edwards-TAVR presence at national and international conferences.
Collaborates with the training team to ensure integration of current clinical data and insights into training and education curricula and that HCP scientific information needs are met. Through a basic understanding of the clinical development process and active discussions with cross-functional team members, ensure that studies are planned to address clinical claim gaps and develop associated scientific communication plans. Interact with KOLs to learn customer needs, understand scientific gaps, trends, and opportunities for clinical research studies. Maintain and manage all the Medical Affairs digital assets and insure that all the content is current and accurate and address all the internal and external requests for medical information.
Planning: Develop detailed clinical communication annual operating plans consistent with Edwards-TAVR Medical Affairs strategic objectives. Develop plans to address any identified gaps in the clinical data required to support key clinical claims.
Operation: Manage the development of scientific communications (abstracts, publication, presentations etc.) while ensuring compliance with all regulatory requirements.
This includes the development and use of a process to ensure that Edwards-TAVR clinical claims are supported by strong clinical data. Manage and coordinate the regular critical review of published clinical data and sharing main takeaways with cross-functional teams. In collaboration with a cross-functional team, conduct pre-conference assessment of scientific programs to ensure that speakers have access to latest clinical data.
Performance Assessment: Track the clinical communication milestones and ensures timely execution. Develop and use metrics to assess the impact and effective dissemination of Edwards-TAVR contemporary clinical data.
Communication and Reporting: Create and maintain a library of key scientific communications (peer reviewed journal article, presentations, etc.). Provide to a cross-functional team and business partners regular updates on key and relevant scientific communications.
Bachelor degree with 12 years of work experience OR Master's degree with 10 years of related experience working in the life sciences industry. MD or PhD preferred
Excellent analytical and presentation skills to scientific and non-scientific audiences
Experience performing research and/or analyzing clinical research data
Experience working in the field of cardiovascular and the medical device industry
Proven ability to develop relationships with physicians and other Healthcare Professionals
Proven ability to work effectively in a cross-functional environment
Ability to travel up to 40% to meet customers and attend national and international conferences
Scientific Director, Medical Affairs Biostatistics
Janssen Research & Development, LLC., a Johnson and Johnson Company is hiring a Director, Medical Affairs Biostatistics to be located in Titusville, NJ or Raritan, NJ and may require up to 10% travel.
Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.JanssenRnD.com for more information.
In this position you will supporting Medical Affairs in the Oncology therapeutic area, you will provide critical statistical oversight to Medical Affairs clinical studies and will assume a leadership role in clinical trial and/or patient registries planning (mostly Phase 3b/4 trials or observational studies for post marketing commitments/requirements) and reporting related activities. You will also assume the role of a Statistics representative for cross-functional teams and work on several trials (projects) simultaneously.
Provide statistical input for clinical trials, observational studies and other types of clinical research projects including but not limited to post-hoc analyses, investigator initiated studies, publications, and HECOR/Epidemiology/Market Access support.
Contribute/lead clinical study design, analysis planning and for the development of statistical analysis plan (SAP) and data presentation plan (DPS) for MA studies.
Provide input to product development and performs statistical functions for submission related activities. Provide statistical support to other disciplines related to clinical statistics (e.g., HECOR/Epidemiology and publication activities).
Serve as a primary contact with outside investigators (and vendors) in the preparation of scientic presentations and manuscripts.
Interact with external Key Opinion Leaders (KOLs).
Pursue rigorous statistical analyses in support of business-critical new research ideas.
Explore and implements innovative statistical methods.
Represent department in meetings with regulatory agencies.
Ph.D. in Statistics or related field with a minimum of 8 years relevant experience .
Experience working in Medical Affairs Statistics is preferred
Experience in the area of Oncology clinical research is required .
Experience in other therapeutic areas such as; Infectious Diseases and Vaccines and Immunology is desirable.
In-depth working knowledge of statistical software such as SAS, R, is required.
Intermediate to advanced proficiency level in applied biostatistical methodology with emphasis on pharmaceuticals is required.
Demonstrated experience as an individual contributor is required while managing workflow in a crossfunctional matrix organization is preferred.
Experience and knowledge of Good Clinical Practices and regulatory requirements for clinical drug development, including the conduct of clinical trials is required.
Excellent verbal and written communication skills, including formal presentation skills is required.
Experience presenting to technical and lay groups at public meetings is required.
Written skills as evidenced by publication and journal articles is preferred.
Ability to successfully multi-task and work independently, under minimal supervision; excellent teamwork skills are required.
Ability to influence, negotiate and communicate with both internal and external customers is required
United States-New Jersey-Titusville-
Janssen Research & Development, LLC. (6084)
Medical Scientific Liaison Manager (M/W) Cardio Metabolic (Befristung)
Gebiet: Wien, Niederösterreich, Steiermark, Burgenland, Kärnten
Wohnort: idealerweise Wien
Ansprechpartner für medizinisch-wissenschaftliche Fragestellungen im Bereich Cardio Metabolic
Aufbau und Betreuung der Medical Stakeholder in der o.g. Region
Professionelle Unterstützung der relevanten Fachgruppen
Enge Zusammenarbeit und Abstimmung mit den Field Project Managern
Interdisziplinäre Zusammenarbeit mit Kollegen aus klinischer Forschung, Market Access, Marketing und Sales sowie mit internationalen Kollegen
Aufbereitung und Präsentation medizinisch-wissenschaftlicher Inhalte
Initiierung und eigenverantwortliche Betreuung medizinischer Projekte
Vorbereitung und kompetente Umsetzung von Fach-Präsentationen
Mitbetreuung klinischer Prüfungen (z. B. bei Selektion der Ärzte für klinische Studien)
Medical Event-Organisation und Betreuung (Round Tables, lokale Fortbildungen etc.)
Medizinisch fachliche Schulung und Weiterentwicklung des Außen- und Innendienstes
Teilnahme an nationalen (und internationalen) Kongressen
Medical Scientific Liaison
817 million. That's how many lives our products touched in 2018. And while we're proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you're given opportunities to explore the power of digital and data.
Where you're empowered to risk failure by taking smart risks. And where you're surrounded by people who share your determination to tackle the world's toughest medical challenges.
We are Novartis. Join us and help reimagine medicine
Your responsibilities include, but not limited to:
1.Contribute to mapping/profiling of KOL/decision makers in line with segmentation.
2.Develop professional relationships, build advocacy and gain contributions of KOL/ decision makers.
3.Collect, analyse and report insights (i.e. CRM System) that may impact Novartis development plans /trial designs.
4.Provide and discuss scientific information and data to healthcare professionals to ensure quality and accuracy of medical and scientific information on new treatment options including Novartis products and selected areas of therapeutic interest.
5.Liaise and provide up-to-date medical support to relevant external groups to facilitate listing of products in medical guidelines, formularies to impact pricing and health-economic discussions.
6.Provide speaker training to health care professionals to support the best use of new therapies developed and commercialized by Novartis. Clinical Development Support
7.Contribute to the identification of appropriate clinical investigators and facilitates placement into Novartis sponsored clinical trials.
8.Provide medical support and training (i.e. disease state and product) to Novartis colleagues (e.g. sales reps, CRAs, etc.)
Medical And Scientific Affairs Director, CGM
More specific responsibilities include, but are not limited to:
Continue to establish Nova Biomedical as a leading diabetes care products provider globally.
Develop relationships with and grow our network of key medical and scientific opinion leaders in diagnosis and management of diabetes.
Develop, define and implement clinical protocols to achieve the medical and regulatory affairs objectives for these evaluations and clinical trials and manage and monitor the execution of all studies.
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.
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.
Endocrinologist PhD, MD, MD/PhD with 5+ years of relevant experience in diagnosis and management of diabetic patients; prior experience with CGM clinical trials and post market studies is essential.
Prior experience in performing or managing clinical trials/evaluations for regulatory submissions and/or market development
Experience in preparing scientific papers for publication in peer reviewed journals
Strong expertise in presenting at meetings and giving seminars
Multi-lingual fluency is a plus
Ability to travel at least 50% is necessary
Medical / Scientific Director
The Medical Director will be responsible for leading the medical writing activities for multiple projects: developing clinical document strategy with minimal supervision while working cross-functionally and with a high level of independence. Responsible for ensuring high quality with regard to scientific content, organization, clarity, accuracy, format, consistency, and adherence to regulatory and internal guidelines, styles, and processes.
Essential Duties and
- Serving as medical point person on assigned accounts
- Developing and writing medical content for multiple and wide-ranging therapeutic areas
- Adding value to current project quality and outcomes by demonstrating in‑depth technical expertise of assigned therapeutic category areas
- Developing credible content for a full range of deliverables (manuscripts, slide presentations, advisory boards, posters, strategy guides, monographs, etc)
- Reviewing medical content for scientific accuracy and appropriateness
- Providing medical insights during brand planning and strategic development meetings
- Work closely with account and strategic services for the assigned account
- Oversee all projects within the account to ensure consistency and accuracy
- Mentor junior writers
- Interact and work directly with clients
- Provide strategic direction across projects
- Discussing medical content with pharmaceutical clients, medical professionals, KOLs, and managed care customers
- Working closely with both account and creative teams to create content that meets the objectives of strategic imperatives
- Working closely with editorial to ensure scientific and editorial accuracy of jobs
- Attending medical, legal, regulatory review meetings
- Participating in project kick-off meetings, weekly status meetings, and scientific services team meetings
- Contributing ideas for brainstorming sessions and participating in new business proposals
- Responding to needs of team and senior management
- Contributing original ideas for tactical planning within assigned accounts
- Advanced degree in life sciences, PhD, PharmD is preferred. MD or DO will be considered with relevant experience.
- At least 5 years' experience in medical education/medical communications with experience leading promotional medical writing activities for multiple projects
- Experience in providing strategic direction across projects is required
- Experience in oncology or managed markets is required
- Strong written and verbal communication skills
- Comfortable speaking with clients and healthcare professionals
- Ability to provide independent medical direction
- Experience with oncology or managed markets is preferred. If the candidate has no experience in managed markets, interest in pharmaceutical managed care marketing is required.
- Ability to travel up to 10%
Competitive salary and benefits package
Scientific Medical Writer, Phd
The Senior Medical Writer researches, writes, and edits scientific reports. Prepares reports, summary documents, and other documents that may be submitted for publication and/or presentation.
Work in a collaborative team to develop conference materials (abstracts, posters, presentations), marketing materials, and peer reviewed publications.
Work closely with Natera's Clinical Affairs, Research and Development, Marketing, and medical education teams.
Draft, edit, and submit abstracts, posters, slide presentations, and manuscripts targeted for publication in peer reviewed journals.
Participate in the writing, editing, and confirmation of the scientific accuracy of marketing and medical education materials, including white papers.
Perform data analysis as needed and develop related graphics and figures.
Interact with internal stakeholders and with external service providers to ensure the timely development, review, and publication of documents.
Work with third parties including academic partners, key opinion leaders, and contractors during development of technical documents.
Bachelor's degree in Biology, Molecular Genetics, Chemistry, Molecular Biology, other relevant scientific discipline, or equivalent required. Advanced degree preferred; Doctoral degree (PhD, MD or PharmD) a plus.
Minimum of 5 years of related experience of which, a minimum of 2 years of experience writing/editing scientific documents/publications experience in the biotechnology, pharmaceutical, medical device, or medical communications industries. Time spent writing in graduate school or during a postdoc does NOT count.
Experience or background in molecular biology/genomics, oncology, prenatal testing, or diagnostics a plus.
Experience submitting abstracts and manuscripts to congresses and journals.
KNOWLEDGE, SKILLS, AND ABILITIES
Excellent writing ability with strong editorial and formatting skills.
Ability to create high quality documents that effectively and clearly convey scientific data, properly identify/target the audience for each document, and communicate key messages clearly and concisely.
Strong interpersonal, communication, and organizational skills.
Ability to work cross functionally, collaborate, negotiate with and influence stakeholders at all levels of the organization.
Ability to read the primary literature and analyze data.
Basic to intermediate knowledge of biostatistical and clinical research concepts.
Familiarity with electronic literature search tools and obtaining copyright permissions.
Strong Microsoft Office (Word, Excel, PowerPoint) skills; experience using Adobe Creative Suite/Creative Cloud (Illustrator, Professional, and InDesign) a plus.
PHYSICAL DEMANDS AND WORK ENVIRONMENT
Duties are typically performed in an office setting and environment.
This position requires the ability to use a computer keyboard, communicate over the telephone and read printed material.
Duties may require working outside normal working hours (evenings and weekends) at times.
Driven by the passion for elevating the science and utility of genetic testing, Natera is committed to helping families identify and manage genetic diseases. Natera is a rapidly-growing diagnostics company with proprietary bioinformatics and molecular technology for analyzing DNA. Our complex technology has been proven clinically and commercially in the prenatal testing space and we are actively researching its applications in the liquid biopsy space for developing products with oncology applications.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits. Healthy catered lunches, Premium snacks and beverages, Onsite gym with cardio and weight-training equipment, Game room with satellite TV, Onsite dry cleaning and alteration service with pick-up and delivery, Employee-organized sport leagues, Happy hours and BBQs, Generous Employee Referral program.
For more information, visit www.natera.com.
Natera is proud to be an Equal Opportunity Employer.
Manager, Global Scientific Communications
The Manager, Scientific Communications, provides support to the Associate Director/Director for the development and execution of the global communications strategy and publications plan for the assigned franchise and product(s). The Manager is responsible for the development of materials to be used for communications and clinical findings to external audiences. Engages with internal stakeholders that include research, medical, marketing, biostats and medical affairs, as well as external authors, investigators, publishers, and medical communications agencies. The Manager ensures the timely execution of the publication plan by writing, reviewing, editing, revising and placing high quality, and impactful scientific and clinical abstracts, posters, oral presentations and manuscripts. analyzes, interpret, and summarizes scientific and clinical data, and helps identify appropriate publication and presentation forums for the data. Develops and maintains global slide decks. Supports the implementation of the medical education plan within the disease area. Conducts literature searches and interprets scientific literature, and provides assessment of competitor papers, posters and other materials.
Support the Associate Director/Director of Scientific Communications in the development of a comprehensive strategic publication plan and ensure implementation for the assigned franchise and product(s)
Responsible for the planning, producing, writing, revising and placing of abstracts, posters, manuscripts from Alexion sponsored clinical trials
Develop high-quality scientific content by means of all necessary research, scientific writing, editing, and fact checking, to meet deadlines while working within project scope and objectives
Manage and track the publication plan to ensure its timely execution
Work with external authors, investigators and thought leaders on abstracts, posters, oral presentations, manuscripts, review articles and slide decks
Coordinate internal and external reviews and collate reviewers' comments; ensure review and approval of publications in accordance with Alexion SOPs
Analyze, interpret, and summarize scientific and clinical data; identify appropriate publication and presentation forums for the data
Assist Associate Director or Director in the development, coordination and execution of medical education strategies such as symposia and CME activities, including agenda development, review of content, slide review and speaker management
Provide oversight of agency maintenance of documents in publication planning software, ensuring database accuracy and integrity,
Conduct literature searches and interpret scientific literature for internal stakeholders, including competitor assessments
Ensure compliance with Alexion Publication Policy
Advanced degree: PhD, PharmD, or MD
1-3years of relevant experience in a Pharmaceutical company or Medical Communications agency
Ability to interpret and organize highly complex scientific data, including experience reviewing clinical trial data and output from statistical analysis programs
Must be skilled writer with demonstrated ability to write / review / edit / place scientific articles, abstracts, posters
Ability to work with teams, including medical publications agencies, write and develop abstracts, posters, oral presentations, manuscripts, slide decks and content for scientific and educational programs
Ability to travel (US and International) as necessary
Must have strong project management skills and ability to successfully manage assignments on time with high quality
Ability to travel (US and International) approximately 10-15% of time
PhD/PharmD in life science
Understanding of the clinical development process, especially clinical study and global health outcome data
Experience in or exposure to strategic and tactical publication planning and the planning of medical educational materials
Experience in working closely with KOLs and authors
Exposure to current good publication practices and guidelines
Boston, MA, United States
Some opportunities happen only once in a lifetime - like a job where you have the extraordinary opportunity to change lives. At Alexion, such opportunities arise through our unwavering mission to serve patients and families affected by rare diseases. These patients are our guiding star, and we act with integrity, urgency, and discipline because we know their lives are at stake.
Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases through the discovery, development and commercialization of life-changing therapies. As the global leader in complement biology and inhibition for more than 20 years, Alexion has developed and commercializes the first and only approved complement inhibitor to treat patients with paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and anti-acetylcholine receptor (AchR) antibody-positive generalized myasthenia gravis (gMG). Alexion also has two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare metabolic disorders, hypophosphatasia (HPP) and lysosomal acid lipase deficiency (LAL-D). In addition, the company is developing two late-stage therapies, a second complement inhibitor and a copper-binding agent for Wilson disease. Alexion focuses its research efforts on novel molecules and targets in the complement cascade and its development efforts on the core therapeutic areas of hematology, nephrology, neurology, and metabolic disorders. Alexion has been named to the Forbes list of the World's Most Innovative Companies seven years in a row and is headquartered in Boston, Massachusetts' Innovation District. The company also has offices around the globe and serves patients in more than 50 countries.
Alexion's aspiration is to be the most rewarding place to work, where people are empowered to make a difference and where diversity of backgrounds and ideas is encouraged. We are looking for talented individuals who share our passion and commitment to change the lives of patients with rare diseases. We hope you will consider joining our team. Further information about Alexion can be found at: www.alexion.com.
As a leading employer in our industry, Alexion is proud to offer a highly competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families. Benefits include group medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more.
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