Jobs · Healthcare · Maryland

Clinical Research Coordinator

Flourish Research · Bowie, MD · 3 wk ago
On-siteHealthcare$33–$38/hrFull-time

About the Job

We are actively hiring a Clinical Research Coordinator to support our Bowie, MD site.

Shift: Monday-Friday, normal work hours

Location: Onsite

FLSA Classification: Non-Exempt

Compensation: $33 to $38 per hour

Essential Job Functions

  • Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
  • Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs
  • Obtain informed consent per federal regs, GCP, and IRB requirements
  • Ethically recruit qualified subjects to meet enrollment timelines
  • Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies
  • Schedule and conduct visits per protocol timelines
  • Protect confidentiality per HIPAA and all confidentiality agreements
  • Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor
  • Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies)
  • Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy
  • Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies
  • Represent Flourish professionally in all interactions

Requirements

  • Bachelor's degree preferred, but not required
  • Must have oncology clinical research experience
  • Minimum of two years of clinical research experience
  • Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections
  • Familiar with e-source reporting via an electronic platform
  • A clear understanding of ICH, FDA, and GCP regulations
  • Impeccable organizational skills and attention to detail
  • Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
  • An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
  • High-level critical thinking skills
  • Working knowledge of medical terminology and lab collection/processing/storage procedures
  • Proficiency with computers and Microsoft Office Suite

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