Job Description
We are seeking detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trial activities, ensuring strict adherence to GCP guidelines, regulatory requirements, and study protocols. You will play a critical role in coordinating all aspects of clinical research — from participant recruitment to data management and compliance monitoring — to support the delivery of groundbreaking medical advancements.
This is an exciting opportunity to work at the intersection. Of healthcare innovation, patient care, and research excellence in a collaborative, fast-paced environment.
Job Responsibilities
* Coordinate and manage the day-to-day operations of clinical studies
* Recruit, screen, and consent eligible study participants in accordance with IRB-approved protocols
* Maintain accurate and up-to-date source documentation and electronic data capture (EDC) systems
* Monitor patient safety, schedule study visits, and ensure protocol adherence
* Liaise with principal investigators, sponsors, and ethics committees
* Prepare regulatory documentation, site initiation, and close-out reports
* Track study progress and submit timely updates to stakeholders
* Ensure quality assurance and compliance with ICH-GCP, MHRA, and institutional regulations
Requirements
Required Skills
* In-depth knowledge of GCP, clinical research regulations, and ethical standards
* Experience with clinical data collection, source documentation, and informed consent processes
* Proficiency with electronic data capture systems (e.g., REDCap, Medidata, or similar)
* Strong organizational and time management skills
* Excellent communication and interpersonal abilities
* Detail-oriented and able to handle multiple trials simultaneously
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Desired Skills
* Bachelor’s degree in Life Sciences, Nursing, or Health Sciences
* ACRP or SOCRA certification
* Previous experience in oncology, cardiology, or rare disease clinical trials
* Familiarity with clinical trial software platforms and regulatory submissions
Benefits
Job Benefits
* Competitive salary with annual performance bonuses
* Training and career development in clinical operations and trial management
* Private health insurance and pension plan
* Supportive work environment with flexible working options
* Work with a cross-disciplinary team of clinical and research experts