A company is looking for a Program Support Specialist to provide operational and documentation support across clinical and program activities.
Key Responsibilities
Develop and organize essential study documents for Trial Master File (TMF)
Initiate sponsor review processes for Adverse Events and Protocol Deviations
Align SOPs with REDCap processes and conduct data entry spot checks
Required Qualifications
Bachelor's degree in public health, life sciences, global health, or a related discipline
Minimum of 7 years of relevant experience
Experience with clinical research operations and TMF documentation
Familiarity with REDCap and SOP management
Strong organizational skills and ability to work independently
Program Support Specialist • Fort Lauderdale, Florida, United States