Research Services Clinical Sciences Professional OPEN RANK (Intermediate – Senior)

Key Responsibilities

• Aid in and oversee the day-to-day operations of clinical trials and studies.
• Obtain study subject’s medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subject to participate in clinical trial.
• Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent forms are filed as required.
• Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the details of the studies through phone contacts and personal interviews.
• Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
• Collect, code, and analyze data obtained from research in an accurate and timely manner.

Senior Level Only

• Assist with developing or developing protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs).
• Maintain subject level documentation and prepare documents, equipment and/or supplies.
• Assist with identifying issues related to operational efficiency and share results with leadership.
• Collect information to determine feasibility, recruitment and retention strategies. Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention.
• Serve as a resource and participate in study initiation and close out duties.

Qualifications

• Intermediate Level: Bachelor’s degree in any field. One (1) year clinical research or related experience.
• Senior Level: Bachelor’s degree in any field. Two (2) years clinical research or related experience.

Preferred Qualifications

• Bachelor’s degree in science or health related field.
• Three (3) years of clinical research or related experience.
• Experience with electronic data capture systems (e.g. EMR or EHR and data management systems).