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Clinical Research Coordinator at Open Systems Technologies

Clinical Research Coordinator

Open Systems Technologies Evansville, IN Contractor
$27.00/ hour
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Clinical Research Coordinator (CRC)

$27/HR (Overtime Available: $40.50/HR)

Evansville, IN 47714

These openings are for a Covid vaccination trial. The client is a global contract research organization providing comprehensive, integrated drug development, laboratory, and lifecycle management services. These will be full time 40 hours a week on site M-F.

They are targeting candidates with current CRC experience at least 1 year of experience and prefer experience with sponsor driven studies.

The CRC conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants.


  • Conducting a clinical research study
  • Participate in clinical research studies
  • Implement clinical research patient care via the research protocol
  • Impact clinical research patient charges
  • Resolve clinical research patient accounts
  • Ascertaining patient eligibility for clinical trials
  • Reviewing study protocols in the conduct of clinical research
  • Perform clinical research and coordinate research activities
  • Develop clinical study budgets based on proposed study protocols
  • Create informed consent forms for trials
  • Manage clinical research projects via study protocols and provide direct patient care for study participants
  • Visit clinical trial sites to ensure conformance with study protocol
  • Set up and maintain clinical databases per study protocol
  • Execute study visits and perform study procedures
  • Screen, consent and enroll patients into oncology clinical research trials
  • Determining eligibility of patients for clinical trials
  • Oversee clinical trials to meet regulatory requirements
  • Obtain informed consent, screen and enroll patient research subjects in suitable studies/clinical trials
  • Educate patients and family regarding particular study and clinical drug trials
  • Maintain clinical research professional credentials

Recommended skills

Clinical Research
Clinical Trials
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