Clinical Research Coordinator
About the Company
We are seeking a detail-oriented and motivated Clinical Research Coordinator (CRC) to support the planning, execution, and management of clinical trials. This role is ideal for candidates with foundational to intermediate experience in clinical research who are looking to grow their careers in a fast-paced, compliance-driven environment. The CRC will work closely with investigators, sponsors, and study participants to ensure trials are conducted ethically, efficiently, and in accordance with regulatory guidelines.
About the Role
This role is ideal for candidates with foundational to intermediate experience in clinical research who are looking to grow their careers in a fast-paced, compliance-driven environment.
Responsibilities
- Coordinate and manage day-to-day clinical trial activities from study start-up to close-out
- Screen, recruit, and enroll study participants according to protocol criteria
- Obtain informed consent and ensure participant understanding of study procedures
- Schedule and conduct study visits, including data and sample collection
- Maintain accurate and up-to-date study documentation, including source documents and case report forms (CRFs)
- Ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and institutional policies
- Communicate effectively with investigators, sponsors, and clinical trial stakeholders
- Track and report adverse events and protocol deviations
- Assist with monitoring visits, audits, and regulatory inspections
- Manage study supplies, investigational products, and lab samples
- Support Institutional Review Board (IRB)/Ethics Committee submissions and correspondence
Qualifications
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, Public Health, or a related field
Required Skills
- Knowledge of clinical trial processes and regulatory requirements (GCP, ICH guidelines)
- Strong organizational and time management skills
- Attention to detail and accuracy in documentation
- Excellent interpersonal and communication skills
- Ability to work independently and as part of a multidisciplinary team
- Proficiency in Microsoft Office and clinical trial management systems (CTMS) or electronic data capture (EDC) systems
Preferred Skills
- Certification such as ACRP-CP, CCRC, or equivalent
- Experience with multiple therapeutic areas or phases of clinical trials
- Familiarity with regulatory submissions and audit processes
Ready to Take the Next Step? Email your updated resume to: