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Clinical Research Coordinator (CRC)
Job summary
A biotech company is seeking a motivated Clinical Research Coordinator (CRC) based in Abu Dhabi, UAE, to support clinical trials. The ideal candidate will coordinate daily study operations, ensuring compliance with protocols and regulations. A bachelor's degree in life sciences or related field, along with a minimum of 3 years of relevant experience, is required. Proficiency in English and Arabic, and GCP certification are mandatory. Join a collaborative team and contribute to advancing regenerative medicine.
Benefits
Qualifications
- Minimum 3 years of experience in clinical research coordination (preferably in pharma, biotech, or CRO).
- Strong understanding of ICH‑GCP, DOH/IRB procedures, and ethical research conduct.
- Proficiency in English and Arabic.
Responsibilities
- Coordinate and support all clinical trial activities from site initiation to close‑out.
- Ensure accurate, timely data entry and documentation in compliance with ICH‑GCP and DOH requirements.
- Act as primary liaison between the clinical site, monitoring team, and clinical operations team.
Skills
Education
Tools
Location: Abu Dhabi, UAE (work conducted across participating clinical sites)
Company: Cellcolabs Clinical (UAE)
About Cellcolabs Cellcolabs is a biotech company specializing in industrial GMP production of high-quality Mesenchymal Stromal Cells (MSCs) to make advanced cell therapies accessible at scale. Building on over 20 years of stem cell research at Karolinska Institutet, Sweden, we are driving a global series of clinical trials to advance MSC-based treatments for various indications.
Role Summary We are looking for a motivated and detail-oriented Clinical Research Coordinator (CRC) to support the conduct of Cellcolabs’ clinical trials in the UAE. You will coordinate daily study operations at local clinical sites, ensuring full compliance with study protocols, ICH‑GCP, and local authorities. You will work closely with investigators, site staff, and Cellcolabs’ Clinical team to ensure smooth study execution and high-quality data collection.
Key Responsibilities
- Coordinate and support all clinical trial activities from site initiation to close‑out.
- Ensure accurate, timely data entry and documentation in compliance with ICH‑GCP and DOH requirements.
- Assist investigators with participant screening, informed consent, and study visit procedures.
- Maintain essential documents and site files in alignment with Cellcolabs’ Clinical Quality Management System.
- Act as primary liaison between the clinical site, monitoring team, and clinical operations team.
- Support monitoring visits, audits, and inspections to ensure site readiness and regulatory compliance.
Qualifications
- Bachelor’s degree in life sciences, nursing, pharmacy, or related field.
- Minium 3 years of experience in clinical research coordination (preferably in pharma, biotech, or CRO).
- Strong understanding of ICH‑GCP, DOH/IRB procedures, and ethical research conduct.
- Excellent communication, organizational, and interpersonal skills.
- Proficiency in English and Arabic.
- GCP certification (mandatory) and ability to work independently in a fast‑paced, collaborative environment.
- Vaid UAE driving Licence
Why Join Us At Cellcolabs, you will be part of an innovative, mission‑driven team accelerating the future of regenerative medicine. We offer a collaborative work culture, professional growth opportunities, and a chance to make a real difference in patients’ lives.
Let’s recruit together and find your next colleague.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.