Non-licensed Clinical Research Coordinator 1, Surgery
About The Position
The Department of Surgery is seeking a Clinical Research Coordinator 1, Non-Licensed to conduct a variety of clinical trial activities. Duties will include working with research participants, processing laboratory specimens, document preparation, record keeping, materials preparation, and reviewing of prospective research participants. The incumbent will assist with clinical trial related activities, recruit, screen and consent potential study participants, schedule study visits, prepare and maintain study documentation, collect data at all study visits, compile adverse event data, and manage all data collected. Additionally, the incumbent is expected to complete on call rotations. Individuals seeking this position must have strong organization skills, have the ability to problem solve, work well in a team environment, have excellent written and oral communication skills, strong assessment skills and demonstrate an ability to learn new information quickly. Additionally, qualified candidates must be able, with training, to collect, process and ship biomarkers, including blood and other body fluids.
Requirements
- Bachelor's Degree Required or equivalent combination of experience, education and or certifications.
- None. Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.
- Strong organization skills
- Ability to problem solve
- Ability to work well in a team environment
- Excellent written and oral communication skills
- Strong assessment skills
- Demonstrate an ability to learn new information quickly
- Able, with training, to collect, process and ship biomarkers, including blood and other body fluids.
Nice To Haves
- Some experience in a healthcare setting
- Knowledge of medical terminology
Responsibilities
- Recruit, screen, and enroll study participants who meet research criteria. Collect basic information through scripted interviews and answer general questions.
- Obtain informed consent from study participants and maintain telephone and in-person contact. Notify Principal Investigator and supervisor of subject status.
- Collect subject data, enter and analyze data, and compile reports, adhering to proper research protocols. Prepare documentation, reports, graphs, and other materials. Keep appropriate logs, track participants, and prepare study materials.
- Process, prepare and ship laboratory specimens.
- Submit study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor.
- Obtain medical histories and conduct medical assessments of clinical trial subjects, including symptom management with appropriate referral. Create treatment plans and serve as an information resource for trial subjects.
- Perform physical exams, including assessing vital signs and administering prescribed medications.
- Conduct adverse event assessment and provide recommendations to Principal Investigator or physicians.
- Complete on call rotations.
Benefits
- Benefited position
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
