Job Details

Job Description

We are seeking a detail-oriented and highly organized Clinical Research Coordinator (CRC) to manage and support clinical trials in accordance with regulatory requirements, study protocols, and ethical guidelines. The ideal candidate will coordinate study activities, ensure data integrity, and act as a liaison between investigators, sponsors, and regulatory bodies.
Key Responsibilities

• Coordinate and manage day-to-day operations of clinical research studies
• Ensure compliance with study protocols, GCP, ICH guidelines, and regulatory requirements
• Screen, recruit, and enroll eligible study participants
• Obtain and document informed consent from participants
• Maintain accurate and complete study documentation and regulatory files
• Schedule and coordinate study visits, procedures, and follow-ups
• Collect, verify, and enter clinical data into study databases and CRFs
• Monitor participant safety and report adverse events per protocol
• Coordinate with investigators, sponsors, CROs, and ethics committees/IRBs
• Prepare for site monitoring visits, audits, and inspections
• Manage study supplies, investigational products, and accountability logs
• Assist in study close-out activities and final reporting

Required Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, Public Health, or related field
• 1-3 years of experience in clinical research or clinical trials (preferred)
• Strong knowledge of GCP, ICH, and regulatory guidelines
• Excellent organizational, communication, and documentation skills
• Ability to manage multiple studies and meet deadlines
• Proficiency in MS Office and clinical data management systems

Preferred Qualifications

• Certification such as CCRC or CRC (SOCRA / ACRP)
• Experience working with IRB/EC submissions
• Familiarity with EDC systems and trial management software

Key Skills & Competencies

• Attention to detail and accuracy
• Strong interpersonal and communication skills
• Problem-solving and time-management abilities
• Ethical judgment and confidentiality
• Ability to work independently and as part of a multidisciplinary team

Work Environment

• Clinical research sites, hospitals, or research institutions
• May require flexible working hours based on study requirements

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Nationality

Any

Iqama

Resident