Job Description
Job Description
Medical Reviewer/Safety Reviewer III - Scientific Content and Medical Affairs Review
Location: 100% remote. Candidates must be located in the US and able to work without visa sponsorship.
Length of Assignment: Through December 31, 2027
Pay Rate: $45-50/hr (depending on candidate location and benefits preference)
Schedule: Part-time, Monday-Friday; flexible schedule with an estimated average of 15 hours per week. Hours may increase or decrease based on business needs and review demand.
Job Description: The Medical Reviewer provides scientific and medical review support for Medical Affairs, Commercial, and cross-functional initiatives. The role reviews scientific content, evaluates clinical data, and provides balanced medical perspectives to ensure the accuracy, quality, and consistency of materials. It requires close collaboration with medical, regulatory, legal, and commercial stakeholders and sound scientific judgment in a fast-paced pharmaceutical environment.\n
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\n - Review scientific, clinical, and medical materials for accuracy, balance, and appropriate interpretation of clinical data.
\n - Evaluate complex clinical study results, publications, and data analyses to support informed decision-making.
\n - Provide medical and scientific input on promotional and non-promotional materials.
\n - Collaborate with Medical Affairs, Commercial, Regulatory, Legal, and other stakeholders.
\n - Ensure content is supported by scientific evidence and aligned with applicable company standards and industry requirements.
\n - Identify scientific inaccuracies, data-interpretation concerns, or compliance risks and recommend appropriate solutions.
\n - Communicate medical and scientific concepts clearly to technical and non-technical audiences.
\n - Participate in ad hoc review projects and support business priorities as needed.
\n - Maintain attention to detail while managing multiple reviews and competing priorities.
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The ideal candidate critically assesses clinical data, provides thoughtful, evidence-based recommendations, and works collaboratively and independently in a dynamic pharmaceutical environment.\n
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Qualifications: I. Required Qualifications
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\n - Strong medical and scientific background, with the ability to evaluate and communicate complex medical information.
\n - Experience interpreting complex clinical data, including clinical trial results, publications, and real-world evidence.
\n - Strong written and verbal communication, collaboration, and stakeholder management skills.
\n - Advanced degree in life sciences, pharmacy, medicine, nursing, or a related healthcare field; PharmD, MD, DO, PhD, PA, NP, or an equivalent qualification preferred.
\n - Pharmaceutical industry experience required.
\n - Demonstrated attention to detail and sound scientific and professional judgment.
\n - Ability to work independently in a remote environment and manage workload effectively.
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II. Preferred Qualifications
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\n - Previous medical review experience in a pharmaceutical, biotechnology, or healthcare organization.
\n - Experience supporting Medical Affairs, Medical/Legal/Regulatory (MLR) review processes, or similar review functions.
\n - Familiarity with regulatory and compliance considerations for scientific communications.
\n - Prior experience working as a medical reviewer with the hiring organization.
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People are our business
worldwide
\n Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.
Job Tags
Part time, Work at office, Remote work, Worldwide, Visa sponsorship, Work visa, Monday to Friday, Flexible hours