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Clinical Trial Medical Reviewer (CNS Studies)
This consulting opportunity supports one or more CNS clinical trials by providing independent medical review, protocol oversight, and clinical guidance to investigative sites. The role helps ensure patient eligibility, protocol compliance, and overall study quality.
Key Responsibilities
- Review patient eligibility before randomization to ensure protocol inclusion and exclusion criteria are met.
- Verify diagnoses and supporting clinical documentation.
- Provide medical guidance to investigative sites on protocol-related clinical questions.
- Review clinical documentation and case report forms (CRFs) to support study quality.
- Serve as an independent medical reviewer across one or more CNS clinical trials.
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Qualifications
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- MD (Psychiatrist) preferred, or Psychiatric Mental Health Nurse Practitioner (PMHNP) with significant psychiatric clinical trial experience.
- Direct clinical experience treating patients with major depressive disorder (MDD), ADHD, anxiety disorders, and/or binge eating disorder.
- Experience in pharmaceutical, biotech, CRO, or research-site clinical trials, including protocol interpretation, patient eligibility review, and CRF assessment.
- CNS clinical research experience is required; psychiatric therapeutic expertise is strongly preferred.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
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