ID: 7057810 (Ref.No. 310070JC)
Posted: June 14, 2019
Application Deadline: Open Until Filled
The Dan L. Duncan Comprehensive Cancer Center (DLDCCC) has an immediate opening for a Clinical Research Coordinator. This position is within the Clinical Trials Support Unit (CTSU) of the DLDCCC, and will provide support for CTSU-coordinated clinical trials. This individual must be a flexible and detail-oriented professional who can quickly adapt to a variety of situations.
- Provide general research coordinator support for the conduct of clinical trials, under the supervision of senior research staff.
- Screen and recruit patients for participation in clinical trials.
- Discuss trials with patients, obtain informed consent, and enroll patients.
- Schedule patient appointments, tests, and procedures according to protocol requirements.
- Collect, review, and submit research data to study sponsors, either via paper or electronic CRFs.
- Ensure accurate study records, and maintain proper study documentation.
- Enter data into study database and/or electronic case report forms.
- Conduct all study activities in compliance with federal and institutional regulations.
- May perform venipuncture (blood draws), EKGs/ECGs, and obtain vital signs for study participants. (Employees may be required to receive on the job training of phlebotomy and EKGs/ECGs prior to performing on study participants).
- May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol.
- Plan and schedule upcoming research visits for study subjects, according to protocol requirements.
- Order supplies and equipment.
- Conduct all testing procedures required by study protocol.
- Under the supervision of more experienced staff, may provide Investigators with guidance regarding protocol requirements.
- Assist other research personnel with reports to regulatory agencies, such as the IRB, FDA and Data and Safety Review Committee.
- May provide guidance and training to junior clinical research coordinators.
- Maintain working knowledge of current protocols, and internal SOPs.
- Under the supervision of more experienced staff, will assist with preparing for audits, inspections, and monitoring visits from regulatory agencies or sponsors.
- Assist with data collection and reporting of Serious Adverse Events to appropriate regulatory agencies and sponsors.
- Attend continuing education and training opportunities relevant to job duties.
- Bachelor's degree in related field or four (4) years of directly related work experience in lieu of a degree.
- Two years of relevant experience in addition to any educational requirements.
- Oncology experience
This is an exempt position with flexible requirements regarding time. The employee is expected to perform job requirements as needed, maintaining flexible hours to complete tasks in progress.
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