Senior Manager - Medical Writing

March 7

🗻 New Hampshire – Remote

Although this job is listed in New Hampshire, this company may be open to hiring remote in other states.

💵 $121k - $159k / year

⏰ Full Time

🟠 Senior

✏️ Content Writer

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Teva Pharmaceuticals

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Teva Pharmaceuticals is a global leader in the pharmaceutical industry, specializing in the development, production, and marketing of generic and specialty medicines. They are dedicated to providing quality healthcare solutions to patients around the world, emphasizing innovation and access to effective medications. With a strong commitment to sustainability, Teva aims to improve health outcomes through their diverse portfolio of products and services.

generic medicines • specialty medicines • CNS • active pharmaceutical ingredients • respiratory

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

💰 Post-IPO Equity on 2023-11

📋 Description

• As a Senior Manager in Global Regulatory Medical Writing, you will write and edit clinical regulatory documents, including submission summaries and other complex materials essential for drug development and product registrations. • You will provide intermediate-level oversight, guidance, and resource management to ensure the effective production of high-quality clinical research documentation. • Focus on product and program-level responsibilities, providing leadership and accountability for key regulatory documents. • Potentially oversee direct reports, contingent workers, and/or vendors, while also offering training and resource management support. • Provide strategic supervision, leadership, and planning for the development of clinical regulatory documents. • Write and edit various types of clinical regulatory documents, ensuring content is accurate, complete, and adheres to regulatory guidelines and editorial standards. • Ensure documents are clear, consistent, and align with regulatory medical writing best practices, including appropriate context and scientific messaging. • Contribute to the preparation and revision of document templates, enhancing process efficiency and quality.

🎯 Requirements

• PhD or PharmD in Life Sciences (or related field) with a minimum of 4 years of experience, or a Master’s degree in Life Sciences (or related field) with at least 6 years of experience. • Preferred experience: 4-6 years in regulatory medical writing. • Proficient in Microsoft (MS) Word and adept at using software, templates, and electronic formats for document preparation. • Recognized as a competent manager with advanced expertise in regulatory medical writing. • Skilled in writing and editing various types of clinical regulatory documents, ensuring clarity, accuracy, and compliance with regulatory guidelines. • Advanced understanding of global regulations and guidelines for document submissions, therapeutic areas, statistical concepts, and product development. • Strong English language proficiency, both written and spoken.

🏖️ Benefits

• Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls. • Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan. • Time Off: Paid Time Off including vacation, sick/safe time, caretaker time, 13 paid Holidays and 3 paid floating holidays. • Life and Disability Protection: Company paid Life and Disability insurance. • Additional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible, Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.