Clinical Research Coordinator - Pharmaceutical Trials

Placements24; Lorenziberg; On-site; EUR 16,000 - 29,000; Full time

Job summary

Placements24 is seeking a diligent Clinical Research Coordinator to support daily trial activities in Queenstown, Eastern Cape. You will work with investigators, participants, and regulatory bodies to ensure protocol adherence and data integrity.

Ideal candidates will have strong knowledge of medical terminology, research methodologies, and ethics in clinical trials, with hands-on experience in coordinating participant visits and data collection.

Qualifications

• Experience coordinating clinical research studies.
• Understanding of medical terminology and research methodologies.
• Ability to recruit and obtain informed consent from participants.

Responsibilities

• Coordinate and manage day-to-day activities of clinical research studies as per protocol.
• Recruit, screen, and enroll eligible participants for clinical trials.
• Obtain informed consent from study participants and ensure their safety and rights are protected.
• Schedule and conduct participant visits, including medical history, physical examinations, and laboratory tests.
• Administer study medications and collect data accurately and efficiently.
• Maintain comprehensive and accurate study documentation, including source documents and CRFs.
• Monitor study progress, identify potential issues, and implement corrective actions.

Skills

Clinical research coordination

GCP compliance

Data collection

Job description

About the Role

Our client, a leading pharmaceutical research organization, is actively seeking a dedicated and meticulous Clinical Research Coordinator to join their expanding team in Queenstown, Eastern Cape. This vital role involves supporting the execution of clinical trials for innovative new therapies, ensuring adherence to protocols, regulatory guidelines, and ethical standards. The successful candidate will work closely with investigators, study participants, and regulatory bodies to manage all aspects of trial conduct. This is a challenging yet rewarding opportunity for an individual passionate about advancing medical science and improving patient outcomes in the Queenstown, Eastern Cape area. A strong understanding of medical terminology and research methodologies is essential.

Key Responsibilities

• Coordinate and manage day-to-day activities of clinical research studies as per protocol.
• Recruit, screen, and enroll eligible participants for clinical trials.
• Obtain informed consent from study participants and ensure their safety and rights are protected.
• Schedule and conduct participant visits, including medical history, physical examinations, and laboratory tests.
• Administer study medications and collect data accurately and efficiently.
• Maintain comprehensive and accurate study documentation, including source documents and case report forms (CRFs).
• Monitor study progress, identify potential issues, and implement corrective actions.