Senior Medical Writer

TalentBurst, an Inc 5000 company; San Rafael (CA); Hybrid; USD 125,000 - 150,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Senior Medical Writer in San Rafael, CA. This role involves drafting regulatory documents and clinical study reports, requiring a background in medical writing and relevant experience. With a hybrid work arrangement and a contract duration of 12+ months, it offers a competitive hourly pay rate.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• Degree with a scientific focus.
• At least 6+ years of experience required.
• Certification from a recognized medical writers association is desirable.

Responsibilities

• Drafts and edits regulatory submission documents like CTDs.
• Responsible for clinical study documents including protocols.
• Reports on safety and efficacy information for pharmaceuticals.

Skills

Medical writing career development

Scientific communication

Education

Bachelor's or higher degree

Job description

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TalentBurst, an Inc 5000 company provided pay range

This range is provided by TalentBurst, an Inc 5000 company. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$50.00/hr - $70.00/hr

Position: Senior Medical Writer

Location: San Rafael, CA, Hybrid (1-2 days in office to align with company policy).

Duration: 12+ Months Contract

Role Description

Seeking candidates who are regulatory medical writers (not Medical Communication)

EDUCATION & SKILLS:

• Bachelor’s or higher degree; scientific focus desirable.
• Evidence of medical writing career development is desirable, e.g., American or European Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through the Drug Information Association.
• At least 6+ years of experience required

Fulfills one of the following:

• Medical writer in the pharmaceutical industry
• Medical or scientific writing experience as a primary job responsibility

Key Responsibilities

• Drafts and edits documents used for submissions including CTDs and RtQs
• Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms
• Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.)

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Writing/Editing, Science, and Research

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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