What are the responsibilities and job description for the Associate Principal Scientist, General Medicine Medical Writing position at MERCK?
Job Description
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The Associate Principal Scientist, General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and external investigators to write or facilitate the writing of timely, peer-reviewed journal articles, conference abstracts, and posters / oral presentations that report results from our company's General Medicine clinical trial program, as well as select early-stage development projects and other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our Research & Development Division colleagues from Global Clinical Development, the Center for Observational and Real-World Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs, and Global Regulatory Affairs and Clinical Safety to identify key issues for publications, define hypotheses and sources of data, and review data analysis plans.
Primary Responsibilities
- Be intimately familiar with science and literature and develop and maintain an awareness of key data and insights within assigned therapeutic area(s) / product(s) to convey our Research & Development Division data effectively and appropriately in peer-reviewed publications.
- Be knowledgeable and conversant with most complex issues / questions in assigned therapeutic area(s) / product(s) to support discussions with our Research & Development Division colleagues and external investigators and thought leaders at a peer level.
- Prepare manuscripts and congress abstracts, posters, and oral presentations for assigned therapeutic area(s) / product(s) in a manner compliant with company policies and industry standards.
- Collaborate with the Publication Manager and members of the Publication Team(s) for assigned therapeutic area(s) / product(s) to develop the Publications Strategy Plan.
- Review and critique publication drafts produced by contracted publication agency partners within assigned therapeutic area(s) / product(s) to ensure quality and consistency (as needed).
- Ensure that information for assigned projects is entered in all relevant databases and repositories, including iEnvision, in an accurate and timely manner.
- Present and defend data at scientific forums and participate in Company-organized meetings, domestic and international (as needed).
Educational Qualifications
Required Experience and Skills
US and Puerto Rico Residents Only :
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Expected US salary range : $135,500.00 - $213,400.00.
Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days.
Employee Status : Regular
Relocation : No relocation
VISA Sponsorship : No
Travel Requirements : 10%
Flexible Work Arrangements : Hybrid
Job Posting End Date : 01 / 7 / 2025
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Salary : $135,500 - $213,400
