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Clinical Research Coordinator

Posted: May 13, 2024
Salary:US$30.00 - US$40 per hour
Job type: Contract
Discipline:Clinical Research
Work Location:On-site

Job description

Are you a CRC with 2+ years of experience and are wanting to gain CRO experience? This is the PERFECT opportunity for you!!

Must Haves:

  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
  • Minimum 2 years as a Clinical Research Coordinator

Important Details:

  • 100% ON SITE
  • Up to 18 hours per week, open to candidate preferences but NO weekends or evenings, must be during business hours


Clinical Research Coordinators (CRC) perform protocol specific duties relevant to the clinical trial in a defined scope that assists the site with patient recruitment.

Scope of Support:

  • Administrative Support customized site level support, such as support with regulatory document submissions and perform chart reviews/EMR interrogation
  • Prescreening including review of concomitant meds, medical history, and inclusion/exclusion criteria to identify potential patients
  • Scheduling Visits including appointment reminders
  • Data Entry and Query Resolution based on data available in source documents and ensure data entry and responses are completed within protocol designated windows
  • External Referral Outreach including grassroots effort to distribute study recruitment materials in and around sites, community outreach
  • Contact, prescreen, and schedule referrals from outreach campaign
  • Conduct Study Visits
  • Perform ICF process following GCP

Qualifications and Functions for this Role:

  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
  • Minimum 3 years in Clinical Research and preference for relevant healthcare experience
  • Certification of CCRC or CCRP preferred
  • Experience of EDC entry and query resolution preferred
  • Knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Comprehensive knowledge of GCP and ICH guidelines
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
  • Preference for Phlebotomy Certification