Clinical Research Coordinator
Posted Updated
Description
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
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