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채용Prime Medicine

Senior Manager, Medical Writing

Prime Medicine

Senior Manager, Medical Writing

Prime Medicine

Watertown, MA

·

On-site

·

Full-time

·

1mo ago

보상

$153,096 - $188,095

복지 및 혜택

Healthcare

401(k)

Equity

Unlimited Pto

Gym

필수 스킬

Medical Writing

Clinical Documentation

Regulatory Writing

Scientific Writing

Data Interpretation

Company Overview:

Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types.

Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology & oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit www.primemedicine.com.

Position Summary

Prime Medicine is seeking a Senior Manager, Medical Writing to support the development of high-quality clinical, regulatory, and scientific documents across our gene-editing pipeline. This role will be both hands-on and strategic, contributing directly to authorship while helping to build scalable medical writing processes in a rapidly growing organization.

Reporting to the Head of Medical Writing, this individual will partner closely with Clinical Development, Regulatory Affairs, Research, and other cross-functional teams to ensure accurate, consistent, and timely documentation supporting global clinical trials and regulatory submissions.

This is an excellent opportunity for an experienced medical writer who thrives in a collaborative, fast-paced biotech environment and wants to grow into increasing leadership responsibility.

Key Responsibilities

Medical Writing & Content Development

  • Serve as primary author and/or lead writer for key clinical and regulatory documents, including:

  • Clinical Study Protocols and Amendments

  • Investigator’s Brochures (IBs)

  • Clinical Study Reports (CSRs)

  • IND/CTA submission documents and briefing packages

  • Critically analyze and interpret nonclinical, clinical, and external literature data to develop clear scientific narratives, conclusions, and messaging.

  • Ensure consistency of content, data interpretation, and scientific positioning across documents and programs.

Cross-Functional Collaboration

  • Work closely with Clinical Development, Clinical Operations, Regulatory Affairs, CMC, Nonclinical, and Quality teams to:

  • Drive document timelines

  • Resolve data and messaging questions

  • Ensure regulatory and scientific alignment

  • Lead and participate in cross-functional document review meetings and support responses to health authority questions as needed.

Process, Quality & Infrastructure

  • Support the development and maintenance of:

  • Medical writing templates, style guides, and standards

  • Document workflows, timelines, and best practices

  • SOPs and quality control processes

  • Perform or oversee document QC, ensuring accuracy, clarity, formatting consistency, and compliance with internal standards and regulatory expectations.

  • Evaluate and incorporate new writing support tools, including AI tools, to streamline processes and improve writing quality.

  • Contribute to inspection readiness and submission quality initiatives.

Leadership & Development (scope dependent on level)

  • May mentor junior writers, contractors, or co-ops as the team grows.

  • Provide guidance on best practices in medical writing, document planning, and scientific storytelling.

Required Qualifications

  • Advanced degree or bachelor’s/master’s degree in life sciences, health sciences, or a related field.

  • ~5+ years of medical writing experience in biotech/pharma OR ~7+ years of writing experience in biotech/pharma or other scientific or academic setting. Includes document ownership and cross-functional leadership

  • Strong experience authoring clinical and regulatory documents (protocols, IBs, CSRs, IND/CTA content).

  • Solid understanding of clinical development and regulatory frameworks (FDA, EMA, ICH).

  • Excellent written, verbal, and organizational skills with strong attention to detail.

  • Proficiency with document authoring tools (e.g., Microsoft Word, Office suite, Share Point, Adobe).

Preferred Qualifications

  • Experience supporting gene editing/therapy or biologics programs.

  • Familiarity with rare disease clinical development.

  • Experience contributing to submissions across multiple development stages.

  • Comfort working in a hands-on, fast-moving biotech environment.

The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).

Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.

Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.

U.S. Pay Range**$153,096—$188,095 USD**
Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.

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Prime Medicine 소개

Prime Medicine

Biotechnology company.

51-200

직원 수

Cambridge

본사 위치

리뷰

3.9

10개 리뷰

워라밸

3.8

보상

3.2

문화

4.3

커리어

3.5

경영진

2.4

72%

친구에게 추천

장점

Supportive and collaborative team

Flexible work arrangements and good work-life balance

Interesting and challenging projects

단점

Poor management communication and organization

Limited career advancement opportunities

High workload and occasional long hours

연봉 정보

17개 데이터

Director

Director · DIR. OF BUSINESS DEVLP, HEAD OF ALLIANCES & CORP. INITIATIVE

2개 리포트

$273,000

총 연봉

기본급

$210,000

주식

-

보너스

-

$273,000

$273,000

면접 경험

62개 면접

난이도

3.7

/ 5

소요 기간

14-28주

합격률

30%

경험

긍정 69%

보통 21%

부정 10%

면접 과정

1

Phone Screen

2

Technical Interview

3

System Design

4

Behavioral

5

Team Fit

자주 나오는 질문

Tell me about a challenging project

System design question

Coding problem

Why this company