Job Summary
Coordinates implements and assists with technical and administrative details involved in clinical research studies including inperson and virtual (e.g. phone online video conference) interactions with research participants. Assists the site Principal Investigator in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures. Responsibilities will include enrolling participants collecting data and interacting with other research staff. This position will also include supervising participants performing the study exercise intervention.
Responsibilities
Screen health records of potential participants for study eligibility based on study criteria Complete medical chart reviews Conduct telephone calls to potential participants to introduce the study perform study screening offer the opportunity to enroll in the study and schedule initial inperson screening visits Communicate with participants medical team for study clearance Perform screening and assessment visits Consent and enroll participants Assist in scheduling participants for followup study treatment and assessment visits Data entry into study databases (e.g. REDCap excel electronic data capture) Documentation of all communications with study participants Explain the study protocol and inclusion criteria to physicians patients and health care providers in person and by phone Communicate with potential referral sources to aid in recruitment Collect and record required data on paper and/or in electronic form Work with research teams and clinicians to meet enrollment goals and study deadlines Identify and report adverse events and protocol deviations Attend team and study meetings Work with confidential health information and complete the necessary training to do so Assist with overall project management Perform other duties as needed Assist with preparation of Institutional Review Board applications and renewals Assesses protocol for clarity and subject safety reviews inclusion/exclusion criteria; clarifies concerns and questions with site Investigator and sponsor. Determines length of visits and coordinates related facility and equipment availability. Reports and tracks adverse events (AE). Reports all AEs to IRB and sponsor. Documents all protocol deviations reconciles test article accountability at study close out and prepares summary report for sponsor. Completes audits corrects CRFs relays CRFs to sponsor. Maintains documents as required by study single IRB and NIH guidelines. May ensure proper collection processing and shipment of specimens. Communicate proficiently in English Supervise the study exercise sessions ensuring compliance with the study protocol This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties responsibilities and qualifications required of employees assigned to the job.
Minimum Qualifications
This position is patientsensitive and must fulfill all associated requirements. We protect our patients coworkers and community by requiring all patientsensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.