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Clinical Research Coordinator

Posted: May 13, 2024
Salary:US$30.00 - US$40 per hour
Location:Hollywood
Job type: Contract
Discipline:Clinical Research
Reference:226604_1715649354
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

Description:

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