Clinical Research Coordinator (Charleston, SC) at Piper Companies
Charleston, South Carolina, USA -
Full Time


Start Date

Immediate

Expiry Date

14 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 Charleston, SC. The Clinical Research Coordinator will ideally have at least two years of clinical research experience. This position is on-site in Charleston, SC.

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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