Senior Feasibility Specialist
Job Summary: Independently sources and analyzes data to develop site, country and investigator strategy or recommendations for proposals and post-award feasibility offerings.
Responsibilities include compiling feasibility reports, presentations, questionnaires and feasibility site assessment based on internal metrics and investigator feedback on study design and logistics, as well as enrollment projection potential, worldwide.
What You'll Do:
* Advise project teams on all Feasibility activities and/or strategy for clinical studies.
* Research and apply critical thinking and analysis on the information available for therapeutic area(s), regarding incidence, prevalence, standard of care, factors determining and influencing indication frequency and distribution, treatment trends, competing trials, etc.
and to be able to clearly justify CTI recommendations on site, country or investigator.
* Carry out database(s) and literature search(s) whenever required, in the case where this search has been completed, apply detailed analysis skills to identify suitable sites for the project in question.
This will include but not be limited to:
+ Perform searches on Investigators by country or by specialty.
+ Perform analysis on past recruitment rates by indication/ country etc.
+ Provide metrics for RFIs/ Proposals, as required.
+ Provide metrics on Investigator Performance.
* Provide quality oversight of project feasibility trackers across the department to ensure projects are meeting timelines and objectives and the trackers are kept up to date and are accurate.
Take any necessary action with the assigned feasibility specialist to update incorrect or missing information in real time.
* Create/coordinate the development of site surveys/questionnaires to obtain key information (e.g., investigator feedback on projected enrollment, feasibility of the study, and site capabilities).
Review the protocol, seeks expertise from applicable supporting functions (Clinical Monitoring, TSL, Medical, CPM, Contracts, RASSUS, etc.), and finalizes draft for sponsor review, as required.
Works with CPM to obtain client approval of the study specific feasibility questionnaire, as needed.
* Create online survey (e.g., Survey Monkey) based on the approved questionnaire to facilitate the collection of data in the most efficient manner.
Track responses of the survey results to compile information for decision making.
* Oversee the site information collection process and assess and analyze compiled information to identify trends and site capabilities, to interpret data, write reports, and make actionable recommendations.
* Conduct timely site follow-up on all aspects of the feasibility process to ensure due diligence follow up is occurring and provide excellent communication back to sites regarding project status.
* Entry of feasibility and maintenance of key data into CTI feasibility database to ens...
- Rate: Not Specified
- Location: Covington, US-KY
- Type: Permanent
- Industry: Finance
- Recruiter: CTI Clinical Trial Services, Inc.
- Contact: Not Specified
- Email: to view click here
- Reference: SRFEA001854
- Posted: 2026-05-30 07:38:35 -
- View all Jobs from CTI Clinical Trial Services, Inc.
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