Senior Clinical Research Associate (Pharmaceuticals)

Placements24; Kimberley; Híbrido; CAD 60.000 - 94.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Retirement plan

Paid time off

Professional development

Descripción de la vacante

Placements24 is seeking a Senior Clinical Research Associate to oversee clinical trials from Kimberley, South Africa. You will identify sites, initiate and monitor visits, ensure GCP compliance, and manage data integrity with cross-functional teams.

The role requires a Life Sciences degree (advanced degree preferred), 5+ years of CRA experience in pharma, and willingness to travel. You will collaborate with investigators, monitor safety, and contribute to study documentation in a fast-paced

Formación

• Bachelor’s degree in life sciences or nursing; advanced degree preferred.
• 5+ years as a Clinical Research Associate in pharma.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience in site management, monitoring, and trial conduct.

Responsabilidades

• Identify, evaluate, and select potential clinical trial sites.
• Initiate, monitor, and close-out sites per protocol and regulatory requirements.
• Conduct site visits (on-site and remote) to verify data accuracy and safety.
• Communicate with investigators and site staff; provide training.
• Submit essential documents timely and maintain records.
• Prepare monitoring visit reports and follow-up on action items.
• Collaborate with study teams (project managers, data managers, medical monitors).
• Develop study documents such as monitoring plans and CRFs.

Conocimientos

Communication skills

Attention to detail

Time management

Educación

Bachelor’s degree in life sciences / nursing

Advanced degree preferred

Herramientas

CTMS

EDC systems

Descripción del empleo

About the Role

Our client, a global leader in pharmaceutical research and development, is seeking a highly experienced and motivated Senior Clinical Research Associate (CRA) to oversee clinical trials from their base in Kimberley, Northern Cape . This role is essential for ensuring the successful execution of clinical studies in accordance with protocol requirements, Good Clinical Practice (GCP), and all applicable regulatory guidelines. You will be responsible for site selection, initiation, monitoring, and close‑out activities, ensuring data integrity, patient safety, and timely trial progression. The ideal candidate will possess strong knowledge of clinical trial processes, excellent communication skills, and a meticulous approach to detail. Join our client's dedicated team in Kimberley and play a vital part in bringing innovative therapies to patients.

Key Responsibilities

• Identify, evaluate, and select potential clinical trial sites.
• Initiate, monitor, and close‑out clinical trial sites according to study protocols and regulatory requirements.
• Conduct site visits (on-site and remote) to verify data accuracy, ensure compliance with protocol and GCP, and assess patient safety.
• Manage communication with investigators and site staff, addressing study‑related issues and providing necessary training.
• Ensure timely submission of essential documents and accurate record‑keeping.
• Prepare monitoring visit reports and follow up on action items.
• Collaborate with internal study teams, including project managers, data managers, and medical monitors.
• Contribute to the development of study‑related documents, such as monitoring plans and case report forms (CRFs).

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
• In‑depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
• Proven experience in site management, monitoring, and trial conduct.
• Excellent interpersonal, communication, and negotiation skills.
• Strong organizational skills with a high level of attention to detail.
• Ability to work independently and manage multiple priorities effectively.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Valid driver's license and willingness to travel extensively within the assigned region.

Benefits

• Our client offers a highly competitive salary and benefits package, including comprehensive health insurance, a retirement savings plan, and generous paid time off.
• We provide excellent opportunities for professional development, including training on new technologies and methodologies, and support for professional certifications.
• This role is based in Kimberley, Northern Cape , and offers a chance to work on impactful clinical trials that contribute to medical advancements.
• Enjoy a dynamic work environment with a team dedicated to scientific excellence and patient well‑being.