Clinical Research Coordinator

Mission

Our mission is to ensure the highest standards of patient care and scientific integrity in every study we conduct.

• Coordinate and oversee all aspects of assigned clinical research studies.
• Recruit, screen, and enroll study participants in accordance with protocol requirements.
• Conduct informed consent discussions and ensure proper documentation.
• Schedule study visits and perform follow-up assessments with participants.
• Collect, record, and maintain accurate source documentation and case report forms (CRFs).
• Ensure adherence to study protocols, Good Clinical Practice (GCP), and institutional policies.
• Communicate effectively with investigators, sponsors, and regulatory authorities.
• Manage investigational product accountability and inventory.
• Support monitoring visits, audits, and inspections.
• Assist in report preparation and data analysis as required.

• Bachelor’s degree in Life Sciences, Nursing, Healthcare, or a related field.
• Thorough knowledge of clinical trial processes, GCP, ICH guidelines, and regulatory requirements.
• Strong attention to detail, documentation accuracy, and organizational skills.
• Proficiency with EDC systems and MS Office applications.
• Excellent communication and interpersonal skills.
• Ability to manage multiple studies and prioritize tasks effectively.

• Certified Clinical Research Coordinator (CCRC) credential.
• Experience with Phase I–IV clinical trials.
• Familiarity with IRB submissions and site initiation procedures.
• Prior experience in oncology, pharmaceuticals, or medical device studies.

• Competitive compensation and benefits package.
• Opportunity to contribute to impactful clinical research projects.
• Supportive and collaborative work environment.
• Ongoing professional development and certification support.