Drug Safety Medical Writer

Drug Safety Medical Writer

Contract Type:

Contractor

Location:

New Jersey

Industry:

Pharmaceuticals

Contact Name:

Divna Rosenzweig

Contact Phone:

Date Published:

27-Mar-2026

Consultant Medical Writer (Drug Safety / Pharmacovigilance)

Contract | Variable Hours (Approx. 15–40 hours/week)

Overview

We are seeking an experienced Consultant Medical Writer to support our Drug Safety and Pharmacovigilance (PV) function. This role focuses on the development of safety- and PV-related documents and content, working closely with cross-functional teams to ensure high-quality, accurate deliverables.

This is a flexible, contract-based role with variable hours, typically ranging from 15 to 40 hours per week.


Key Responsibilities

  • Author and contribute to drug safety and pharmacovigilance documentation, including safety sections of regulatory and non-regulatory documents
  • Collaborate with Drug Safety/PV teams to interpret and present safety data clearly and accurately
  • Support the preparation of safety narratives, reports, and other PV-related materials
  • Ensure consistency, scientific accuracy, and clarity across all written deliverables
  • Adhere to internal standards, timelines, and quality expectations

Ideal Candidate Profile

  • Background in Pharmacovigilance, Drug Safety, or Pharmacokinetics (PK/PV)
  • Experience in medical writing with a focus on safety content, either in-house or as an independent consultant
  • May come from a Drug Safety/PV operational role with strong writing expertise and interest
  • Prior experience specifically in regulatory document writing (e.g., protocols, IBs, CSRs) is not required

Skills & Competencies

  • Strong scientific writing and data interpretation skills, particularly in safety contexts
  • High attention to detail and ability to communicate complex information clearly
  • Reliable, responsive, and able to work independently in a remote/consulting environment
  • Effective communicator with collaborative mindset

Technical & Logistical Requirements

  • Access to a Windows-based laptop and familiarity with Microsoft Office tools
  • Comfortable using standard business and document management systems
  • Ability to integrate into an existing team structure and workflows

Additional Notes

  • This role follows the same structure and expectations as other consultant medical writers within the organization
  • Successful candidates will demonstrate performance aligned with high-performing peers in similar writing roles



...

Apply Now
Apply Now

Share this job

Interested in this job?
Save Job
Create As Alert

Similar Jobs

SCHEMA MARKUP ( This text will only show on the editor. )