- 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
- Bristol Myers Squibb (Summit, NJ)
- …here at BMS with our Cell Therapy team. The **Associate, Manufacturing Technical Services** will collaborate with internal Manufacturing partners, such as but not ... + Knowledge of cGMP/FDA regulated industry + Basic mathematical skills + Strong technical and compliance writing capability + Proficient in MS Office applications +… more
- Bristol Myers Squibb (Summit, NJ)
- …our Cell Therapy team. The Sr. Specialist role is a combined role working 50% Technical Writer role and 50% Specialist role within the QA Shop floor Department ... that provides quality oversight in the manufacturing areas of S12. Tech Writer role works independently and is responsible for authoring high-quality documentation… more