Clinical Research Coordinator

Placements24; Gqeberha; Hybrid; ZAR 300.000 - 500.000; Vollzeit

Benefits dieser Stelle

Competitive salary

Health insurance

Professional development

Annual leave

Sick leave

Retirement plan

Flexible work

Supportive team

Zusammenfassung

Placements24 is seeking a meticulous Clinical Research Coordinator for a hybrid role in Port Elizabeth. You will balance on-site patient interactions with remote data management to drive successful clinical trials, ensuring protocol adherence and data integrity.

In collaboration with principal investigators and healthcare teams, you will manage participant logistics, monitor safety, and prepare for monitoring visits. A nursing or life sciences background with GCP knowledge is preferred.

Qualifikationen

• Bachelor's degree in Nursing, Life Sciences, or related healthcare field.
• Minimum 2 years of experience as a Clinical Research Coordinator or in a similar clinical research role.
• Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
• Excellent organizational skills and attention to detail.
• Proficiency in electronic data capture (EDC) systems and electronic medical records (EMR).
• Strong interpersonal and communication skills for effective interaction with participants and healthcare professionals.
• Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.
• Certification as a Clinical Research Professional (e.g., ACRP, SoCRA) is an advantage.

Aufgaben

• Coordinate all aspects of assigned clinical trials according to study protocols, ICH-GCP guidelines, and institutional policies.
• Recruit, screen, and enroll study participants, ensuring informed consent procedures are followed meticulously.
• Schedule and manage participant visits, ensuring adherence to the protocol schedule of events.
• Collect, manage, and maintain accurate and complete clinical trial data, including case report forms (CRFs) and source documents.
• Administer study medications/devices and perform study-related procedures as delegated and trained.
• Monitor participant safety and report adverse events and protocol deviations promptly.
• Liaise with principal investigators, sub-investigators, sponsors, and regulatory agencies.
• Manage study supplies and equipment, ensuring adequate inventory.
• Prepare for and participate in internal and external monitoring visits and audits.

Kenntnisse

Organizational skills

Communication skills

Attention to detail

Multitasking

Ausbildung

Bachelor's degree in Nursing, Life Sciences, or related healthcare field

Tools

EDC systems

EMR

Jobbeschreibung

About the Role Our client, a renowned medical research institute located in Port Elizabeth , is actively seeking a meticulous and dedicated Clinical Research Coordinator to support vital clinical trials. This hybrid role offers the flexibility to balance essential on-site patient interaction and data management with remote administrative and organizational tasks. You will play a crucial role in the successful execution of studies, ensuring compliance with protocols and regulatory standards, and contributing to advancements in patient care. The successful candidate will work closely with principal investigators, healthcare professionals, and study participants, maintaining a high level of organization and attention to detail. This position is ideal for an individual passionate about medical research and eager to contribute to impactful scientific endeavors within a supportive and professional setting.

Key Responsibilities

• Coordinate all aspects of assigned clinical trials according to study protocols, ICH-GCP guidelines, and institutional policies.
• Recruit, screen, and enroll study participants, ensuring informed consent procedures are followed meticulously.
• Schedule and manage participant visits, ensuring adherence to the protocol schedule of events.
• Collect, manage, and maintain accurate and complete clinical trial data, including case report forms (CRFs) and source documents.
• Administer study medications/devices and perform study-related procedures as delegated and trained.
• Monitor participant safety and report adverse events and protocol deviations promptly.
• Liaise with principal investigators, sub-investigators, sponsors, and regulatory agencies.
• Manage study supplies and equipment, ensuring adequate inventory.
• Prepare for and participate in internal and external monitoring visits and audits.

Requirements

• Bachelor's degree in Nursing, Life Sciences, or a related healthcare field.
• Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar clinical research role.
• Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
• Excellent organizational skills and attention to detail.
• Proficiency in electronic data capture (EDC) systems and electronic medical records (EMR).
• Strong interpersonal and communication skills for effective interaction with participants and healthcare professionals.
• Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.
• Certification as a Clinical Research Professional (e.g., ACRP, SoCRA) is an advantage.

Benefits

• Competitive salary based on experience and qualifications.
• Comprehensive health insurance package.
• Opportunities for professional development and specialized training.
• Generous annual leave and sick leave benefits.
• Retirement savings plan.
• Exposure to cutting-edge medical research.
• Supportive team environment.
• Potential for flexible work arrangements.