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Sr. Clinical Trial Specialist
Posted: 05/26/2026
Employment Type:
Contract
Job Category: Operations and Development
Job Number: 5087
Job Description
The Senior Clinical Trial Specialist (Sr. CTS) is responsible for providing logistical support for one or more clinical trials. This position will work closely with cross-functional teams to ensure site start-up through close-out activities are conducted in accordance with Standard Operating Procedures (SOPs) and applicable regulations governing the conduct of clinical trials.
Responsibilities:
Requirements:
Responsibilities:
- Manages region/sites and CRO, under the direction of a Study Lead
- Manages small and large-scope vendors, including oversight of contracts (invoicing, purchase order monitoring, and forecasting)
- Oversee development and maintenance of study documents such as site instructions, site specific informed consent forms, Lab Manual, Pharmacy Binder, Study Reference Manual, study plans, etc.
- Contributes content to team meetings, including Study Management Team meetings
- Participates in Trial Master File completeness reviews and update Essential Document List, may serve as the main study contact for Records Management
- Serve as a subject matter expert for the CTS role on initiatives and working groups
- Mentors Clinical Trial Associates and Clinical Trial Specialists, including onboarding of new hires
Requirements:
- Bachelor’s degree or equivalent is required (scientific or healthcare discipline preferred)
- Typically 4 years of direct work experience in Clinical Research
- Understanding of study phases and general knowledge of how they apply to clinical development
- Able to handle multiple tasks and deadlines, and identify issues and take appropriate actions
- Must be self-motivating and able to develop solutions for a variety of complex problems
- Must have the ability to build and maintain positive relationships with management and peers
- 10% travel may be required