CSS Scientific
Clinical Research Coordinator
CSS Scientific, Charleston, South Carolina, United States, 29408
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.
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.