Job Description

Job Title: Clinical Research Coordinator

Job Overview:

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to support clinical trials and ensure high-quality study execution. This on-site, direct-hire position , based in Charleston, SC , plays a key role in participant recruitment, study coordination, and maintaining compliance with research protocols. The ideal candidate will thrive in a fast-paced research environment, contribute to the success of clinical trials, and build strong relationships with investigators and study participants.

Compensation:

• $60,000 – $65,000 annually

Work Schedule:

• Monday – Friday, standard business hours

Key Responsibilities of the Clinical Research Coordinator:

• Manage study start-up activities, including creating recruitment plans, tools, and progress notes
• Screen and identify potential participants for trials through phone interviews and on-site evaluations
• Maintain accurate records and enter study data into Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), and Case Report Forms (CRF)
• Coordinate participant reimbursements and ensure proper tracking of referral sources
• Prepare source documents and ensure accurate data collection in line with study protocols
• Perform technical procedures as required, such as phlebotomy, EKGs, pulmonary function testing, and other protocol-driven assessments
• Monitor inclusion and exclusion criteria throughout the trial and assist with peer reviews for eligibility
• Document laboratory data, adverse events, and report findings promptly to investigators and regulatory bodies
• Dispense study medication under investigator supervision
• Communicate regularly with investigators, sponsors, and monitors to ensure study progress and compliance
• Attend investigator meetings and maintain ongoing knowledge of protocol requirements

Qualifications and Skills for the Clinical Research Coordinator:

• Bachelor’s degree required
• 2+ years of experience in a clinical research coordinator or similar role
• Strong attention to detail and organizational skills
• Ability to manage multiple studies simultaneously and meet deadlines
• Excellent communication skills for interacting with participants, investigators, and sponsors
• Commitment to a career in clinical research and adherence to regulatory and ethical standards

Why Join Us?

This opportunity offers the chance to contribute to impactful clinical research while developing your career in a collaborative and professional environment. You’ll gain hands-on experience in trial coordination, patient engagement, and protocol management while working with a supportive team that values precision, compliance, and patient care.

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