- Merck & Co. (Rahway, NJ)
- … clinical protocol(s).Serves as the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical /scientific and ... SummaryThis position drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate… more
- TEKsystems (New York, NY)
- … clinical end users and support staff to correct build the technical documentation for various clinical applications. Provide direction and best practices ... Candidates must have experience creating/writing in depth support documentation for clinical applications within Radiation Oncology Description: Our client is the… more
- Merck (Rahway, NJ)
- …for leading medical writing deliverables that support the Translational Medicine clinical writing portfolio. **The Associate Principal Medical Writer :** + ... leads and authors clinical regulatory documents (eg, protocols, pivotal clinical study reports, clinical sections of submission, etc.) across all… more
- Merck (Rahway, NJ)
- …scientist on the clinical trial team. + Collaborates with the Medical Writer on clinical /scientific and regulatory documents. + Partners with Study Manager ... This position drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate… more
