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Manager, Medical Writing

2-6 years
Not Disclosed
10 April 25, 2025
Job Description
Job Type: Full Time Education: PhD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Manager, Medical Writing
Location: Parsippany, United States, New Jersey, 07054
Company: Teva Pharmaceuticals
Job ID: 61672
Date: April 24, 2025


About Teva Pharmaceuticals:
Teva Pharmaceuticals is on a mission to make good health more affordable and accessible, helping millions around the world live healthier lives. The company is a leading manufacturer of generic medicines and a proud producer of products on the World Health Organization’s Essential Medicines List. Teva reaches over 200 million people daily and continues to innovate, seeking passionate individuals to help drive its mission forward.


Role Overview:
Teva is hiring a Manager, Medical Writing in their Global Regulatory Medical Writing team. This position is responsible for writing and editing clinical regulatory documents, such as submission summaries and other complex documents. The role also involves offering leadership, guidance, and strategic assistance in the preparation of clinical research documentation used for drug development and product registrations.


Key Responsibilities:

  • Leadership & Oversight:

    • Oversee contingent workers and vendors; provide training as needed.

    • Offer leadership and basic accountability for clinical regulatory documents.

    • Provide strategic assistance and planning support in clinical regulatory writing.

  • Writing & Editing:

    • Write and edit clinical regulatory documents, ensuring clarity and consistency in medical/scientific messaging.

    • Ensure documents comply with regulatory guidelines, departmental, and editorial standards.

    • Ensure that all documents are accurate, complete, and in the correct context from a regulatory medical writing perspective.

  • Document Templates:

    • Participate in preparing and revising document templates as needed.


Qualifications:

  • Education & Experience:

    • PhD or PharmD with at least 2 years of experience

    • Master’s degree with at least 4 years of experience

    • Bachelor’s degree with at least 6 years of experience

  • Skills & Knowledge:

    • In-depth knowledge of global regulations and guidelines for document submissions.


Travel Requirements:

  • International and domestic travel may be required.

Location:

  • This is a US-Based Remote position, preferably within the US Eastern time zone.

Relocation Assistance & Work Visa:

  • Relocation assistance and work visa sponsorship are not available for this position.


Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment, ensuring all applicants are considered without regard to race, gender, disability, and other protected statuses. The company promotes a diverse and inclusive workplace and offers accommodation throughout the recruitment process.