Medical Monitor
3 weeks ago
Job Description:
- Pay: Open, depending on experience.
- 12-month assignment to start with potential for extension or conversion.
- Open to candidates willing to relocate at their own expense.
- Hybrid, a minimum of 2 days onsite (with the flexibility to adjust due to business needs, required meetings etc.).
- Paid parking is required on-site if driving.
- MD, Ph.D., Pharm.D., or similar.
- This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units.
- Will join a team supporting a clinical program with one phase 2 trial, two core phase 3 and a phase 3 LTS trial (in total, 100 sites globally).
- The role will work closely with two Medical Directors and another Clinical Scientist, supporting data and medical monitoring, preparation of study documents, as well as operational activities related to the conduct of the trials.
- Responsible for reviewing incoming data, listings, and deviations in coordination with Medical Directors.
- Meeting with Medical Directors 2-3 times per week to ensure no items were missed.
- Adverse advent review for multiple studies.
- Experience with quality, deviations, protocols, and consents.
- Must have experience in late-stage clinical trials, medical monitoring, and data reviews.
- Nice to have experience in neurology or neuroscience.
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