Clinical Research Coordinator

Placements24; Soweto; Hybrid; ZAR 360,000 - 600,000; Full time

Benefits offered by this job

Medical aid

Retirement fund

Job summary

Placements24 seeks a dedicated Clinical Research Coordinator for a role in Soweto, Gauteng. You will manage trial operations, recruit participants, and ensure data integrity while adhering to regulatory requirements.

The candidate should be organized, detail-oriented, and passionate about advancing medical research. You will work closely with investigators, study sponsors, and participants to ensure protocol compliance and patient safety, contributing to the successful execution of clinical

Qualifications

• Bachelor's degree in Nursing, Pharmacy, Life Sciences, or related field.
• Experience as a Clinical Research Coordinator or similar preferred.
• Strong understanding of clinical trial processes and GCP guidelines.
• Excellent organizational, time management, and multitasking skills.
• Proficient data entry and management with meticulous attention to detail.

Responsibilities

• Recruit, screen, and enroll eligible participants into clinical trials.
• Schedule and manage participant visits, ensuring protocol requirements are met.
• Administer study medication and conduct study procedures as directed by the investigator.
• Maintain accurate patient data and study records in line with regulatory standards (GCP).
• Monitor participants for adverse events and report them as required.
• Educate participants and families about the study protocol and expectations.
• Maintain communication with investigators, sponsors, and regulatory authorities.
• Ensure compliance with study protocols and institutional policies.

Skills

Regulatory knowledge

Data management

Communication

Organization

Team collaboration

Education

Bachelor's degree in Nursing/Life Sciences

Tools

EDC systems

Job description

About the Role

Our client, a leading clinical research organization focused on advancing medical treatments, is looking for a dedicated Clinical Research Coordinator to join their team in **Soweto, Gauteng**. This role is essential for the successful execution of clinical trials, ensuring patient safety, data integrity, and adherence to protocols and regulatory requirements. The ideal candidate will be organized, detail-oriented, and passionate about contributing to life-saving research. You will work closely with investigators, study participants, and study sponsors, managing various aspects of trial operations. This is a rewarding opportunity to be part of groundbreaking medical advancements right here in **Soweto**. You will play a vital role in bringing new therapies to patients through meticulous trial management.

Key Responsibilities

• Recruit, screen, and enroll eligible participants into clinical trials.
• Schedule and manage participant visits, ensuring all protocol requirements are met.
• Administer study medication and conduct study procedures as directed by the investigator.
• Collect, document, and maintain accurate patient data and study records in accordance with regulatory standards (GCP).
• Monitor participants for adverse events and report them as required.
• Educate participants and their families about the study protocol, procedures, and expectations.
• Maintain effective communication with investigators, study team members, sponsors, and regulatory authorities.
• Ensure compliance with all study protocols, institutional policies, and Good Clinical Practice (GCP) guidelines.
• Manage study supplies and equipment, ensuring proper storage and handling.
• Assist with study close-out activities and archiving of study documents.

Requirements

• A Bachelor's degree in Nursing, Pharmacy, Life Sciences, or a related field.
• Previous experience as a Clinical Research Coordinator or in a similar clinical research role is highly preferred.
• Strong understanding of clinical trial processes and Good Clinical Practice (GCP) guidelines.
• Excellent organizational, time management, and multitasking skills.
• Proficiency in data entry and management, with meticulous attention to detail.
• Strong interpersonal and communication skills, with the ability to build rapport with diverse patient populations.
• Ability to work independently and as part of a collaborative team.
• Knowledge of medical terminology and human anatomy/physiology.
• Experience with electronic data capture (EDC) systems is a plus.
• Residency or strong familiarity with **Soweto, Gauteng** and its surrounding communities is an advantage.

Benefits

Our client offers a competitive salary, comprehensive benefits including medical aid and a retirement fund, and dedicated training programs to support your career growth in clinical research. We promote a supportive and collaborative work environment where your contributions directly impact medical advancements. This role in **Soweto** offers a fulfilling career path for individuals passionate about healthcare innovation and patient care. Join our dedicated team and be a part of the future of medicine.