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Associate Director Principal Medical Writer

0-2 years
$147,000 – $212,333.33
10 Sept. 12, 2025
Job Description
Job Type: Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Associate Director / Principal Medical Writer

Location

Remote, USA
(Proximity to Cambridge/Boston, MA or Morristown, NJ highly desirable for attending occasional team meetings)

Salary Range

USD 147,000 – 212,333.33


At a Glance

Bring your curiosity to a team where deep immunoscience meets cutting-edge innovation. Across oncology, rare diseases, neurology, and vaccines, you’ll be working at the intersection of lab science and AI-powered discovery — collaborating across boundaries to turn breakthrough ideas into real-world impact.

This role offers the opportunity to:

  • Deepen your scientific expertise.

  • Grow as a leader.

  • Collaborate globally.

  • Transform ideas into treatments that change lives.


About the Job

Are you ready to shape the future of medicine?
The race is on to accelerate drug discovery and development, bringing answers to patients and their families.

The Global Medical Writing and Document Management team is dedicated to generating timely, high-quality, cost-effective, and regulatory-compliant documents. Our mission is to synergize with evolving technologies and push the boundaries of regulatory writing.

As an innovative global healthcare company, we pursue one purpose: to chase the miracles of science to improve people’s lives. This is also a place where you can grow and flourish, with countless opportunities to learn, connect, and stretch your potential.


Main Responsibilities

Document Development

  • Create high-quality, regulatory-compliant clinical documents to support the product lifecycle.

(Further detailed responsibilities may include authoring, reviewing, managing submissions, and mentoring — can expand if you’d like full scope.)


Why Work With Us

  • Expand your horizons: Grow through curiosity, supported by mentorship, mobility, and bold development.

  • Accelerate with technology: Use AI and automation to push scientific boundaries and reimagine drug discovery.

  • Impact through inclusive innovation: Help deliver fairer, more accessible outcomes through inclusive research.

  • Turn patient needs into breakthrough science: Drive scientific advances that begin with patients and end with life-changing treatments.


Meet Our People

Nils Libert, Associate Scientist (Belgium)
Nils plays a key role in advancing groundbreaking research — driving innovation, uncovering new scientific possibilities, and contributing to treatments that impact patients worldwide.