NEW JOB OPENING
MEDICAL AFFAIRS MEDICAL WRITER (PHARMA) -SCIENTIFIC WRITING
IN Whippany, NJ, USA!

 

Date Posted: 07/09/2026
Hiring Organization: Rose International
Position Number: 503923
Industry: Biotech/Healthcare
Job Title: Medical Affairs Medical Writer (Pharma) -Scientific Writing
Job Location: Whippany, NJ, USA, 07981
Work Model: Hybrid
Work Model Details: 3 days a week on site
Shift: M-F 8 hour shifts
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 12
Min Hourly Rate($): 45.00
Max Hourly Rate($): 50.00
Must Have Skills/Attributes: Healthcare, Medical Terminology, Pharmaceutical, Science, Writing Skills
Experience Desired: Medical Affairs, Medical Communications, Scientific Affairs, or Clinical Research experience (1-3 yrs); Professional experience in biomedical sciences, pharmaceutical, or healthcare (1-3 yrs); Experience authoring or reviewing scientific documents, publications & medical education materials (1-3 yrs); Strong scientific writing and research skills (1-3 yrs); Proficiency using Microsoft Office, AI-enabled productivity tools (Copilot, Perplexity, ChatGPT) (1-3 yrs)
Required Minimum Education: Bachelor’s Degree

**C2C is not available**

 

Job Description
REQUIRED EDUCATION

• Bachelor's degree in Pharmacology, Biology, Biochemistry, Pharmacy, Medical Sciences, or a related biomedical field.



REQUIRED QUALIFICATIONS

• Approximately 1–3 years of experience in Medical Writing, Medical Affairs, Medical Communications, Clinical Research, or a related pharmaceutical environment.

• Strong scientific writing and verbal communication skills.

• Experience working in regulated healthcare or pharmaceutical environments.

• Highly organized with strong attention to detail and the ability to manage multiple projects simultaneously.

• Comfortable collaborating across cross-functional teams.

• Proficiency with Microsoft Office and AI productivity tools such as Microsoft Copilot, Perplexity, or similar technologies.



SUMMARY

Join the Medical Affairs team as a Medical Writer supporting scientific communications, medical education, compliance initiatives, and Medical Affairs operations. Working closely with Medical Directors and cross-functional partners, you will help develop scientific content, coordinate research-related activities, support governance processes, and manage contracts with healthcare professionals and external vendors.



This is an excellent opportunity for an early-career professional looking to build experience within a global pharmaceutical organization.



RESPONSIBILITIES

• Develop and edit scientific publications, medical training materials, and Medical Affairs documents.

• Conduct literature research and support scientific communication initiatives.

• Assist with publication planning and internal document review processes.

• Support Medical Affairs compliance activities, including SOP updates and governance tracking.

• Coordinate medical inquiries, fellowship programs, and research support activities.

• Manage contracts, purchase orders, and vendor relationships involving healthcare providers, advisory boards, and research partners.

• Collaborate with Medical Directors, Compliance, Legal, Procurement, and other business functions.

• Organize meetings, schedules, and team initiatives to improve operational efficiency.

• Utilize Microsoft Office and AI-powered productivity tools to support document development and workflow management.



***Drug screen & criminal background check will be required

  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**


 

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

 

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About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

I had a very positive experience working for Rose. The entire process is very efficient and easy.

Joanne, Consultant

Working for Rose International was the most pleasant assignment I have ever had. They were always on top of situations when necessary, and very helpful. I was very proud to be an employee of Rose International, and would recommend anyone to try to work with them.

Melvon, Consultant

Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.

David, Consultant

Each time I contacted Rose, I was completely satisfied with the great attention and customer service I received. Each person was extremely knowledgeable and patient with my concerns or questions.

Diana, Consultant

Rose International maintained good communication during assignments and are very informative through email and phone calls.

Sade, Consultant

EMPLOYEE COMMENTS

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