Associate Principal Scientist, General Medicine Medical Writing Job at MSD in Ra

Job Description

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

• MD, PhD, or equivalent in the biological sciences, biostatistics or epidemiology and a minimum of 5 years’ industry experience (biopharmaceutical company and/or communications agency) in scientific writing of peer-reviewed publications or BS/MS and a minimum of 12 years’ experience in scientific writing of peer-reviewed publications.

Required Experience and Skills

• Strong writing skills and competence in biomedical research.
• General Medicine clinical trial publications experience.
• Understanding of clinical research methodology, biostatistics, and clinical pharmacology.
• Proficiency with Microsoft Office programs.

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. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

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.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance.

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.

Employee Status: Regular

Relocation: No relocation

VISA Sponsorship: No

Travel Requirements: 10%

Flexible Work Arrangements: Hybrid

Shift: Not Indicated

Valid Driving License: No

Hazardous Material(s): n/a

Job Posting End Date: 01/7/2025

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