Location: Cambridge
Work Mode: Hybrid (2 days a week in office)

Job Purpose
The Clinical Scientist Specialist contributes to the clinical development strategy and supports the execution of the plan for the assigned molecule(s)/indication(s).

Key responsibilities:

• Clinical Science Support, Data Review & Cross functional Collaboration
• Collaborates with clinical operations, Medical Directors, and other groups etc. in the development of clinical study documents, including protocol, Informed Consent Form (ICF), Case Report Forms (CRFs), Clinical Study Reports, etc.
• Leads and/or contributes to the development of clinical presentations and other documents for internal governance/team meetings or external communications (e.g., Investigator and Steering Committee meetings, study coordinator or clinical research administrator training, study newsletters, communications to study sites, Key Opinion Leader (KOL) interactions, an...