Clinical jobs in Service/Supplier
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This position will support all Quality Assurance GCP activities to ensure quality and compliance of Cidara sponsored clinical trials
Purpose of the Position:The position is responsible for maintaining quality records and operating document control systems for the site to ensure comp
This Requires previous exposure to early clinical trial development.
Plan, conduct, analyze, and report pre-clinical and clinical studies to support U.S. and international registration applications.
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
Position requires previous experience with clinical research, patient care, Clinical Development, Medical/Scientific Affairs, and/or basic research
Assess GCP compliance risk areas and develop and implement risk mitigation measures.
Responsible for verifying clinical compliance to applicable Standard Operating Procedures.
This position will act as a Clinical Research Ethicist.
Receipt and abstraction of protocol and/or contact information into the appropriate databases.
Preparing scientific and regulatory documents on behalf of government and private sector clients for submission to the FDA.
This position will manage and process SAEs; assist in the preparation of reports; generate specified data reports from...
Preparing scientific and regulatory documents.
Perform various tasks in support of clinical research including adverse event analysis and processing...
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.
Robert Half Executive Search has been exclusively retained by an International leader in Biopharma innovation to unearth a talented, Vice President...