Clinical Research Coordinator II at Piper Companies
Rocky Mount, North Carolina, USA -
Full Time


Start Date

Immediate

Expiry Date

13 Dec, 25

Salary

65000.0

Posted On

16 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Piper Companies is seeking a Clinical Research Coordinator II for a globally renowned clinical research organization located in Rocky Mount, North Carolina (NC). The Clinical Research Coordinator will ideally have at least two years of clinical research experience. This position is on-site in Rocky Mount, NC.

Responsibilities of the Clinical Research Coordinator II:

  • Conducts study start-up activities including recruitment planning, tool creation, and participant phone screening.
  • Develops and executes proactive recruitment strategies to meet enrollment targets.
  • Maintains and updates Clinical Trial Management System (CTMS) for participant tracking, reimbursement, and outreach.
  • Performs protocol-specific procedures such as phlebotomy, ECGs, and diagnostic testing as required.
  • Accurately documents study data and adverse events, ensuring timely communication with investigators and sponsors.
  • Builds strong relationships with investigators and sponsors, attending meetings and maintaining ongoing trial communication.

Qualifications for the Clinical Research Coordinator II:

  • Minimum of 2 years as a Clinical Research Coordinator.
  • Bachelor’s degree required.
Responsibilities
  • Conducts study start-up activities including recruitment planning, tool creation, and participant phone screening.
  • Develops and executes proactive recruitment strategies to meet enrollment targets.
  • Maintains and updates Clinical Trial Management System (CTMS) for participant tracking, reimbursement, and outreach.
  • Performs protocol-specific procedures such as phlebotomy, ECGs, and diagnostic testing as required.
  • Accurately documents study data and adverse events, ensuring timely communication with investigators and sponsors.
  • Builds strong relationships with investigators and sponsors, attending meetings and maintaining ongoing trial communication
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