Clinical Research Coordinator at Piper Companies
Raleigh, North Carolina, USA -
Full Time


Start Date

Immediate

Expiry Date

02 Nov, 25

Salary

68000.0

Posted On

04 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Data Integrity, Interpersonal Skills, Cfr, Hipaa, Regulatory Guidelines

Industry

Pharmaceuticals

Description

Piper Companies is seeking a Clinical Research Coordinator for a trusted partner in clinical development located in Raleigh, North Carolina (NC). The Clinical Research Coordinator would ideally have hands-on phlebotomy experience in a clinical site network environment. This position will sit on-site in Raleigh, NC.

Responsibilities of the Clinical Research Coordinator:

  • Support clinical trials by screening participants, confirming eligibility, and performing phlebotomy and specimen processing per protocol.
  • Ensure data accuracy through timely entry and management of case report forms and study records.
  • Mentor junior staff and uphold protocol compliance and quality standards.
  • Maintain regulatory compliance and assist with study start-up, maintenance, and close-out activities.
  • Adapt to dynamic workflows by managing multiple studies and supporting cross-functional research efforts.

Qualifications for the Clinical Research Coordinator:

  • 2-3 years of clinical research coordination experience with strong knowledge of clinical trial protocols and regulatory guidelines (GCP, CFR, HIPAA).
  • Phlebotomy experience is required, along with prior experience as a Medical Assistant, LPN, or RN.
  • Detail-oriented and highly confidential, with a strong commitment to patient privacy and data integrity.
  • Preferred certifications include GCP and Advanced CRC, with demonstrated leadership and interpersonal skills.
Responsibilities
  • Support clinical trials by screening participants, confirming eligibility, and performing phlebotomy and specimen processing per protocol.
  • Ensure data accuracy through timely entry and management of case report forms and study records.
  • Mentor junior staff and uphold protocol compliance and quality standards.
  • Maintain regulatory compliance and assist with study start-up, maintenance, and close-out activities.
  • Adapt to dynamic workflows by managing multiple studies and supporting cross-functional research efforts
Loading...