SocClin Research Specialist
SocClin Research Specialist
Posted on :
16-04-2025
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1 Vacancy
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Job Description
Position Summary
This position will be responsible for overseeing and conducting trials within the Department of SurgeryVascular. The Clinical Research Coordinator is responsible for the planning organization and conduct of multiple clinical research study protocols including independently collecting and recording data project administration and communication with various stakeholders. The specialist is assigned a subset of clinical trials for which they will serve as the primary coordinator. The specialist works with delegated authority from the Principal Investigator to ensure that these clinical trials are conducted in a manner to meet all federal sponsor and university requirements. These trials will not require a RN coordinator for patient enrollment and followup; however the supervisor (Research Nurse Manager) and Principal Investigator will provide support and oversight as needed. The specialist facilitates trial start up works with the supervisor and Pl to develop enrollment/recruitment strategies ensures a full understanding of any clinically related data needs and is available for questions and oversight. The specialist acts as a primary contact for the assigned trials for the sponsor the investigators and subjects; activities include identifying and consenting patients with investigators attending offsite study meetings as required scheduling and completing telephone or research clinic followup visits attending study teleconferences/training facilitating investigator and trials personnel training performing data abstraction and completion of CRFs adverse event/outcome monitoring and reporting maintenance of subject research charts and facilitating study monitor visits. The specialist will also provide backup coverage and support for the clinical trials team members as needed. This includes completion of CRFs data abstraction/data entry conducting subject telephone followup visits and assisting with research clinic visits (scheduling subjects collection/processing/shipment of study lab samples).
Required Qualifications Competencies And Experience
Bachelors degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions. Strong written and verbal communication skills. Must be able to work and communicate with diverse populations effectively and professionally. Ability to work independently as well as function as part of a team. Proficient with Microsoft Outlook Excel and Word.
Preferred Qualifications Competencies And Experience
Previous Coordinator experience. CRC or equivalent certification is not required but preferred.
This position will be responsible for overseeing and conducting trials within the Department of SurgeryVascular. The Clinical Research Coordinator is responsible for the planning organization and conduct of multiple clinical research study protocols including independently collecting and recording data project administration and communication with various stakeholders. The specialist is assigned a subset of clinical trials for which they will serve as the primary coordinator. The specialist works with delegated authority from the Principal Investigator to ensure that these clinical trials are conducted in a manner to meet all federal sponsor and university requirements. These trials will not require a RN coordinator for patient enrollment and followup; however the supervisor (Research Nurse Manager) and Principal Investigator will provide support and oversight as needed. The specialist facilitates trial start up works with the supervisor and Pl to develop enrollment/recruitment strategies ensures a full understanding of any clinically related data needs and is available for questions and oversight. The specialist acts as a primary contact for the assigned trials for the sponsor the investigators and subjects; activities include identifying and consenting patients with investigators attending offsite study meetings as required scheduling and completing telephone or research clinic followup visits attending study teleconferences/training facilitating investigator and trials personnel training performing data abstraction and completion of CRFs adverse event/outcome monitoring and reporting maintenance of subject research charts and facilitating study monitor visits. The specialist will also provide backup coverage and support for the clinical trials team members as needed. This includes completion of CRFs data abstraction/data entry conducting subject telephone followup visits and assisting with research clinic visits (scheduling subjects collection/processing/shipment of study lab samples).
Required Qualifications Competencies And Experience
Bachelors degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions. Strong written and verbal communication skills. Must be able to work and communicate with diverse populations effectively and professionally. Ability to work independently as well as function as part of a team. Proficient with Microsoft Outlook Excel and Word.
Preferred Qualifications Competencies And Experience
Previous Coordinator experience. CRC or equivalent certification is not required but preferred.
Required Experience:
Staff IC
Employment Type
Full-Time
Key Skills
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