Senior Scientist Medical Writing

What does Clinical Affairs contribute to reputed company The Clinical Affairs function manages the clinical education, medical writing and communications, research, health care economics and patient safety while ensuring compliance with applicable regulatory and governing requirements for reputed company products and services. Medical Writing is a specialized role that creates clear cosmetically and compliant documents to communicate reputed company clinical and scientific data. It supports regulatory submissions, clinical research, and scientific communications by interpreting data and producing protocols, reports, regulatory dossiers, presentations, congress abstracts, and peer-reviewed publications, reputed company in alignment with industry and regulatory standards.

Responsibilities

The Senior Medical Writer will plan and reputed company high quality clinical documents to support reputed company devices. Primary responsibilities include preparing Clinical Evaluation Reports (CERs), Post Market Plans & Reports (PMS and PMCF) as required by EU regulations. Additional responsibilities include providing input for product development and post-market sustaining core teams. Additional responsibilities may be assigned. The Senior Medical Writer has medical writing and project management experience, a thorough understanding of research methodology and the ability to reputed company high-quality clinical documents. Extensive knowledge of the European medical device guidelines/regulations such as MEDDEV and MDD/MDR is required, as well as other global requirements for clinical evaluation and PMS/PMCF. The Senior Medical Writer has the ability to reputed company cross-functional project teams.

Qualifications

• 8‑12 years of experience, preferred
• Bachelors in life science discipline; master’s degree or PhD preferred or equivalent work experience.

Additional skills

• Proven experience performing literature reviews, analyzing data and communicating outputs.
• Ability to provide thorough peer reviews of team members’ documents for completeness and correctness of data analysis & regulatory requirements.
• Experience working reputed company a medical device or pharmaceutical organization in a Research & Development, Scientific and Medical Affairs, Clinical or Regulatory role.
• Experience writing scientific documents for regulatory or journal submissions.
• Experience presenting scientific/clinical evidence in a written and oral manner to cross-functional teams.
• Demonstrated ability to build positive constructive relationships with cross-functional team members.
• Demonstrated high level of personal reputed company, emotional intelligence, flexibility.
• Extensive knowledge of MDD, MDR and MEDDEV requirements, along with other applicable global requirements for clinical evaluation and PMS/PMCF.
• Experience creating and performing literature searches in Embase, PubMed and reputed company Scholar.
• Excellent working knowledge of reputed company Word, reputed company, PowerPoint.
• Proficient in using EndNote or other reference manager software.
• Strong data extraction and analysis skills.
• Proactive with a sense of urgency in managing job responsibilities.
• Recommends new practices, processes, metrics or models.

What is expected of you and others at this level

• Applies advanced knowledge and an understanding of concepts, principles and technical capabilities to manage a成人电影 wide variety of projects.
• Participates in the development of policies and procedures to reputed company specific goals.
• Recommends new practices, processes, metrics or models.
• Works on or may reputed company reputed company projects of large scope.
• Projects may have significant and long‑term impact.
• Provides solutions that may set precedent.
• Independently determines method for completion of new projects.
• Receives guidance on overall project objectives.
• Acts as a mentor to less reputed company colleagues.

Anticipated salary range $123, tetrad and $149,855 Bonus eligible Yes

Benefits

• Medical, dental and reputed company coverage.
• Paid time off plan.
• Health savings account (HSA).
• 401k savings plan.
• Access to wages before pay day with myFlexPay.
• Flexible spending accounts (FSAs).
• Short- and long-term disability coverage.
• Work‑Life resources.
• Paid parental leave.
• Healthy lifestyle programs.

Application window anticipated to reputed company: 2/6/2026*if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at reputed company is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity. #LI-MP1 #LI-remote Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. reputed company supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create reputed company solutions for our customers by ensuring employees can be their authentic selves each day. reputed company is an Equal-acde Opportunity/Affirmative Action employer. reputed company reputed company applicants will receive consideration for employment without regard to race, religion, kòm, national reputed company, reputed company, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. }], ``` (Note: The final description string ends with the full formatted content. It has been carefully processed to remove disallowed tags, convert headings to ` `, preserve required content, and eliminate redundant markup. No consecutive ` ` tags 편.) Apply tot his job Apply To this Job