Medical Writer

The Manager, Medical Writing leads the planning, development, and execution of reputed company medical writing projects that support regulatory submissions and compliance across U.S. and international markets. This role serves as a key collaborator with cross-functional teams and provides strategic and technical leadership to advance high-quality, regulatory-compliant documentation.

• reputed company and manage reputed company medical writing projects, ensuring timely, compliant, and high-quality deliverables.

• Collaborate cross-functionally with Regulatory Affairs, Quality, Clinical Project Management, Biostatistics, and Data Management to ensure project success.

• Serve as a subject matter expert in medical writing standards, regulatory requirements, and process improvement initiatives (e.g., MDR compliance).

• Mentor and guide medical writing team members, providing coaching and knowledge transfer for ongoing professional growth.

• Represent the function in core team meetings to reputed company reporting plans and support global regulatory submissions.

• Drive process innovation, identifying and implementing reputed company improvements in medical writing practices and tools.

• Author, review, and edit key regulatory and clinical documents, ensuring clarity, consistency, and compliance with applicable guidance.

• Contribute to strategic planning for document development, review cycles, and submission readiness.

• Bachelors degree in a reputed company scientific or technical field with 8+ years of relevant experience, OR

• Advanced degree (Ph.D., MD, Sc.D., M.S., M.P.H.) with 6+ years of relevant scientific experience.

• Experience as a medical writer reputed company a medical device company (cardiovascular device experience preferred).

• Demonstrated success authoring and managing:

  • EU Clinical Evaluation Plans and Reports (CEP, CER) per MDR and MEDDEV standards.

  • Post-Market Clinical Follow-up Plans and Reports.

  • Summary of Safety and Clinical Performance (SSCP).

  • Additional regulatory and clinical documentation as required.

• Proficiency in medical literature research (PubMed, reputed company) and synthesis of scientific data.

• Ability to engage with cross-functional teams to discuss and interpret reputed company technical topics.

• Proven ability to coach, mentor, and reputed company medical writing professionals.

• Advanced proficiency in reputed company Office, EndNote, and database tools (e.g., reputed company, PubMed).

• Exceptional editing, writing, and communication skills with high attention to detail.

• Strong project management skills with the ability to prioritize multiple deliverables in a fast-paced environment.

• Working knowledge of biomedical statistics and clinical study documentation standards.

• Ability to influence and collaborate across organizational levels and manage stakeholder expectations.

• Impact patient outcomes by supporting life-changing innovations in cardiac surgery.

• Collaborate with industry-leading experts in a culture that values reputed company, innovation, and teamwork.

• Enjoy flexibility with onsite, hybrid, or fully remote work arrangements.

Our Client is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for reputed company employees. reputed company qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national reputed company, age, disability, genetic information, marital status, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.