Clinical Scientist III
4 weeks ago
This position is anticipated to open within the next couple of months**
We are seeking a PhD, PharmD, or MD Clinical Scientist for our Global Pharmaceutical Client in Cambridge, MA. Very attractive pay rate
This role will support a director in the medical scientific contribution to the clinical study (protocol development, validation of study data, review of study plan, managing study committees).
Details:
- 1-year renewable contract
- Hybrid schedule (minimum of 2 days per week onsite at Waters St location in Cambridge)
- This person will join a team supporting global late-phase clinical programs.
Must haves:
- Must have experience in late-stage clinical trials, medical monitoring, and data reviews
- Previous experience with protocol development
- Previous experience in neurology, neuroscience preferred
- Previous senior clinical scientist experience
The primary purpose of the Clinical Scientist’s position is to assist/support the Clinical Research Director in the medical/scientific contribution for the clinical studies e.g: supporting operational activities about the abbreviated protocol/protocol/amended protocol development (such as contribution to the writing of protocol and/or amendments, informed consent, committees charters development, and other study ancillary documents), support in the validation and clinical case review of study data, review of study plans and draft study reports/publications for accuracy, a search of medical/scientific information for study teams, literature review and analysis, assists in the preparation of the responses for investigators, study teams, ethics committees or regulatory authorities, help manage study committees.
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Cambridge, United States Randstad Life Sciences US Full timeThis position is anticipated to open within the next couple of months** We are seeking a PhD, PharmD, or MD Clinical Scientist for our Global Pharmaceutical Client in Cambridge, MA. Very attractive pay rate!This role will support a director in the medical scientific contribution to the clinical study (protocol development, validation of study data, review of...
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