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.