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Found 9 Bachelors Degree jobs
This position will support all Quality Assurance GCP activities to ensure quality and compliance of Cidara sponsored clinical trials
This is a key leadership role at a growing, fast-moving privately held biopharmaceutical company.
Pacific-Link Consulting is seeking a Regulatory Affairs professional with an expertise in CMC who will be responsible for FDA submissions.
Purpose of Position:The Principal Technical Writer is responsible for originating and reviewing analytical documentation in accordance with SOPs in su
Responsible for verifying clinical compliance to applicable Standard Operating Procedures.
Receipt and abstraction of protocol and/or contact information into the appropriate databases.
This position will manage and process SAEs; assist in the preparation of reports; generate specified data reports from...
Primary responsibilities include managing team of 5-7 Clinical Information Specialists...
Process Validation Technical WriterReporting to the Technical Manager, Process Validation, this role will provide support of Process Validation activi
Purpose of the Position:This position based in Milford, MA, implements and supports a Process Safety Management (PSM) system for operations in Milford
At Technical Resources International, Inc. , this position reviews adverse event data to verify accuracy, consistency, and compliance.