Medical Reviewer​/Safety Reviewer III

This contract Medical Reviewer / Safety Reviewer III role provides scientific and medical review support for medical affairs, commercial, and cross-functional initiatives within a fast-paced pharmaceutical environment. You will review scientific and clinical content, evaluate complex clinical data, and offer balanced, evidence-based medical perspectives to ensure the accuracy, quality, and consistency of materials. The position is fully remote with a flexible schedule and an estimated average commitment of approximately 15 hours per week, with hours varying based on business needs.

• Review scientific, clinical, and medical materials to ensure accuracy, balance, and appropriate interpretation of clinical data.
• Evaluate complex clinical study results, publications, and data analyses to support informed decision-making.
• Provide medical and scientific input on both promotional and non-promotional materials.
• Collaborate cross-functionally with Medical Affairs, Commercial, Regulatory, Legal, and other stakeholders to support business objectives.
• Ensure all content is supported by robust scientific evidence and aligned with applicable company standards and industry requirements.
• Identify potential scientific inaccuracies, data interpretation concerns, or compliance risks and recommend appropriate solutions.
• Communicate medical and scientific concepts clearly and effectively to both technical and non-technical audiences.
• Participate in ad hoc review projects and contribute to priority initiatives as business needs evolve.
• Maintain a high level of attention to detail while managing multiple concurrent reviews and competing priorities.
• Support Medical Affairs and Medical/Legal/Regulatory review processes or similar review functions, as needed.
• Apply sound scientific and professional judgment when assessing clinical data and providing recommendations.
• Work independently in a remote setting while effectively organizing and prioritizing workload.

• Advanced degree in a life sciences, pharmacy, medical, nursing, or related healthcare field (such as PharmD or PhD, or equivalent preferred).
• Strong medical and scientific experience with a demonstrated ability to evaluate and communicate complex medical information.
• Experience interpreting complex clinical data, including clinical trial results, peer-reviewed publications, and real-world evidence.
• Pharmaceutical industry experience.
• Excellent written and verbal communication skills.
• Strong collaboration skills and the ability to manage and influence stakeholders across functions.
• Demonstrated attention to detail and the ability to exercise sound scientific and professional judgment.
• Proven ability to work independently in a remote environment and manage workload effectively.
• Experience in medical review, pharmacovigilance, and medical affairs.

• Previous medical review experience within a pharmaceutical, biotechnology, or healthcare organization.
• Experience supporting Medical Affairs and Medical/Legal/Regulatory review processes or similar review functions.
• Familiarity with regulatory and compliance considerations related to scientific and medical communications.
• Ability to critically assess clinical data and provide thoughtful, evidence-based recommendations.
• Comfort working in a dynamic, fast-paced pharmaceutical environment.
• Strong collaboration and cross-functional partnership skills with medical, regulatory, legal, and commercial teams.

This is a fully remote contract position running through December 31, 2027, offering a flexible schedule aligned with business needs. The typical commitment is approximately 15 hours per…