The Technical and Scientific Reviewer provides leadership and strategic direction for scientific and technical content in regulatory documents prepared by the Medical Operations Team.
They are responsible for reviewing, developing, and ensuring the quality of medical and scientific materials, demonstrating expertise across therapeutic areas.
Candidates should possess excellent English writing and proofreading skills, with a clinical, scientific, or research background preferred.
Experience in writing Clinical Evaluation Reports (CERs), literature reviews (e.g., PRISMA, Cochrane), and adherence to ICMJE authorship guidelines is highly valued.
A strong understanding of scientific research, data management, and statistical methods is essential.
Qualifications include a Ph.D./Pharm D plus 1-2 years of experience or a BS/B.Pharm/BSN/MS/MPH with 5-10 years of industry experience.
Strong communication, project management, and proficiency in Microsoft Office and bibliographic software are also required.