Opportunity Description
Job Title: Clinical Trial Specialist
Job Description
The Clinical Trial Specialist is responsible for coordinating the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various boards, preparing study tools, and ensuring informed consent forms are properly managed. The specialist will collaborate with research nurses and physicians to confirm protocol eligibility and manage patient records.
Responsibilities
+ Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and data collection plans are in place.
+ Prepare study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.
+ Develop study tools using computer software such as Excel® and Word®.
+ Collaborate with Research Nurse Clinicians and physicians to review patient charts and medical history for protocol eligibility.
+ Ensure that informed ...
Job Description
The Clinical Trial Specialist is responsible for coordinating the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various boards, preparing study tools, and ensuring informed consent forms are properly managed. The specialist will collaborate with research nurses and physicians to confirm protocol eligibility and manage patient records.
Responsibilities
+ Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and data collection plans are in place.
+ Prepare study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.
+ Develop study tools using computer software such as Excel® and Word®.
+ Collaborate with Research Nurse Clinicians and physicians to review patient charts and medical history for protocol eligibility.
+ Ensure that informed ...
Interested in this opportunity? Apply now through Expertini.
Apply for this Position