Clinical Research Coordinator (CRC)

About PharmaKnowl Consulting

PharmaKnowl is a Saudi-based Contract Research Organization (CRO) and regulatory affairs service provider. The company supports pharmaceutical, biotechnology, and MedTech companies with their research and regulatory needs.

The Role of Clinical Research Coordinator

PharmaKnowl Consulting is seeking a Clinical Research Coordinator (CRC) to join its team in Riyadh, Saudi Arabia. This is a full-time, on-site position. The CRC will be responsible for coordinating day-to-day clinical trial activities, ensuring adherence to approved study protocols and regulatory standards.

Key Responsibilities

• Coordinating participant screening, enrollment, and scheduling in alignment with approved study protocols.
• Organizing and documenting informed consent processes.
• Maintaining accurate study records and source documents.
• Ensuring data collection, entry, and management comply with GCP and SFDA regulatory standards.
• Supporting investigators and monitors during site visits.
• Preparing and updating regulatory and ethics committee submissions.
• Assisting with safety reporting and query resolution.
• Collaborating closely with cross-functional teams.
• Adhering to established timelines for all study activities.
• Providing continuous oversight of site compliance and quality.

Qualifications and Experience

Candidates for the Clinical Research Coordinator position should possess 0-1 years of relevant experience. A strong understanding of clinical trial processes and regulatory requirements is beneficial.

Work Environment

This is a full-time, on-site role based in Riyadh, Saudi Arabia, requiring daily presence at the designated work location. The CRC will work within a collaborative team environment, supporting various clinical trial initiatives.

Application Process

Interested candidates are encouraged to apply for this position. Salary details will be discussed during the interview process.