Instagram
youtube
Facebook

Manager, Medical Writing - Innovative Medicine R&D (Remote, East Coast, Usa)

2-4 years
$111,000 - 146,000
10 March 21, 2025
Job Description
Job Type: Full Time Education: PhD/PharmD/M.Sc 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 - Innovative Medicine R&D (Remote, East Coast, USA)
Date: March 7, 2025
Location: West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 59604

Who We Are:

Teva Pharmaceuticals is a global leader in making good health more accessible and affordable. Operating in nearly 60 countries, we are proud to be the world’s largest manufacturer of generic medicines, with many products listed on the World Health Organization's Essential Medicines List. Every day, 200 million people take one of our medicines. We continue to seek new ways to make a difference and invite new talent to join our journey.

The Opportunity:

As a Manager in Global Regulatory Medical Writing, you will be responsible for writing and editing high-quality clinical regulatory documents, including submission summaries and other complex materials essential for drug development and product registration. You will also provide guidance, oversee resources, and ensure seamless production of clinical research documentation that supports our mission to deliver innovative healthcare solutions.

How You’ll Spend Your Day:

  • Clinical Regulatory Document Writing & Editing:

    • Lead author for clinical regulatory documents, including:

      • Protocols

      • Clinical study reports

      • CTD Clinical Overview (M2.5) and Clinical Summaries (M2.7.1, M2.7.2, M2.7.3, M2.7.4)

      • ISS/ISE

      • Investigator brochures

      • Briefing documents

      • Responses to regulatory authority questions

  • Project Leadership & Accountability:

    • Work independently with minimal supervision.

    • Apply statistical and regulatory concepts in clinical document preparation.

    • Manage multiple documents simultaneously as the lead writer.

    • Provide strategic assistance and planning support for clinical regulatory documents.

    • Lead comment resolution meetings and guide the team toward successful outcomes.

  • Collaboration & Quality Assurance:

    • Collaborate with cross-functional teams to ensure timely delivery of high-quality documents.

    • Ensure documents adhere to applicable regulatory guidelines, departmental, and editorial standards.

    • Contribute to document template preparation and revisions to enhance efficiency.

  • Resource Management & Oversight:

    • May oversee contingent workers and/or vendors, offering training and resource management support.

Your Experience and Qualifications:

  • Education:

    • PhD or PharmD in Life Sciences (or a related field) or a Master’s degree in Life Sciences (or a related field).

  • Experience:

    • PhD or PharmD with at least 2 years of experience, or Master’s degree with at least 4 years of experience.

    • Preferred: 2-4 years of experience in regulatory medical writing.

  • Technical Skills:

    • Proficiency in Microsoft (MS) Word and advanced use of document preparation software, templates, and electronic formats.

    • Expertise in writing and editing clinical regulatory documents, including submission summaries and complex materials.

    • Strong knowledge of government regulations, global submission guidelines, and industry standards.

    • Familiarity with statistical concepts and regulatory requirements for document submission.

  • Other Requirements:

    • Demonstrated ability to contribute to strategy development and problem-solving.

    • Strong communication and collaboration skills to drive alignment and results.

    • Process development, improvement initiatives, and budget planning experience.

Compensation:

  • Annual Salary Range: $111,000 - $146,000 (dependent on geography, skills, education, experience, and other qualifications).

  • This position may also be eligible for a performance-based bonus.

Role Location:

  • US-Based Remote: Preference for Eastern Time Zone candidates.

  • Relocation Assistance and Work Visa Sponsorship Not Available.

Enjoy a More Rewarding Choice:

Teva offers a competitive benefits package, including:

  • Health Insurance: Medical, Dental, Vision, and Prescription coverage starting from day one.

  • Retirement Savings: 401(k) with 6% employer match and an annual 3.75% Defined Contribution.

  • Time Off: Paid Time Off (vacation, sick/safe time, caretaker time), 13 paid holidays, and 3 floating holidays.

  • Life & Disability Protection: Company-paid Life and Disability insurance.

  • Additional Benefits:

    • Employee Assistance Program

    • Employee Stock Purchase Plan

    • Tuition Assistance

    • Flexible Spending Accounts, Health Savings Account

    • Paid Parental Leave, Family Building Benefits, and more.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities regardless of age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national origin, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace.