Senior Pharmaceutical Clinical Research Associate (CRA)

Placements24; Upington; Hybrid; ZAR 700,000 - 1,200,000; Full time

Benefits offered by this job

Health insurance

Retirement contributions

Career development opportunities

Job summary

Placements24 is seeking a Senior Pharmaceutical Clinical Research Associate (CRA) based in Upington, Northern Cape, for a hybrid role balancing field-based monitoring with office or remote work. You will oversee trial conduct, ensure GCP compliance, and act as liaison between sites and sponsor to ensure data integrity and patient safety.

The ideal candidate has 5–7 years of CRA experience, strong ICH/GCP knowledge, and proficiency with CTMS/EDC systems, with willingness to travel regionally.

Qualifications

• Minimum 5–7 years of Clinical Research Associate experience in pharma/biotech.
• Strong knowledge of ICH guidelines and GCP.
• Experience in site monitoring across initiation, routine, and close-out visits.
• Proficient in CTMS and electronic data capture systems.
• Willingness to travel extensively within the assigned region.

Responsibilities

• Conduct site initiation, interim, and close-out visits to ensure GCP compliance.
• Monitor trial sites for data integrity, timeliness, and accuracy.
• Ensure patient safety and rights throughout the study.
• Train site staff on study procedures and regulatory requirements.
• Prepare monitoring visit reports and track action items.
• Collaborate with investigators and sponsor to resolve issues.
• Develop monitoring plans and stay updated on regulations.

Skills

Site monitoring

GCP knowledge

CTMS/EDC experience

Travel readiness

Education

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

Tools

CTMS

EDC systems

Job description

About the Role

Our client, a leading pharmaceutical company renowned for its groundbreaking clinical research, is seeking an experienced Senior Pharmaceutical Clinical Research Associate (CRA) to join their dedicated team. This role, based in Upington, Northern Cape , offers a hybrid work arrangement, allowing for a balance between field-based site monitoring and office-based or remote work. You will be responsible for overseeing the conduct of clinical trials, ensuring adherence to protocols, regulatory guidelines (GCP), and company standards. The ideal candidate will possess strong monitoring skills, excellent communication abilities, and a thorough understanding of the clinical trial process from initiation to closure. You will act as the key liaison between the investigative sites and the sponsor, ensuring data integrity, patient safety, and timely study execution. This is a vital role in advancing the development of new pharmaceutical therapies.

Key Responsibilities

• Conduct site initiation, interim, and close-out visits to ensure compliance with study protocols and GCP.
• Monitor clinical trial sites to verify the accuracy, completeness, and timeliness of data.
• Ensure patient safety and rights are protected throughout the trial.
• Train and support site staff on study-related procedures and regulatory requirements.
• Liaise with investigators and site staff to resolve study-related issues and discrepancies.
• Prepare detailed monitoring visit reports and ensure timely follow-up on action items.
• Review essential study documents and regulatory binders.
• Communicate effectively with project teams, investigators, and other stakeholders.
• Contribute to the development and implementation of study-specific monitoring plans.
• Stay updated on relevant regulations and industry best practices in clinical research.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• A minimum of 5-7 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical or biotech industry.
• Thorough knowledge of ICH guidelines and Good Clinical Practices (GCP).
• Demonstrated experience in site monitoring, including initiation, routine, and close-out visits.
• Strong understanding of clinical trial protocols, data management, and regulatory submissions.
• Excellent interpersonal, communication, and negotiation skills.
• Ability to manage multiple priorities and work independently with minimal supervision.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel extensively within the assigned region as required by monitoring activities.

Benefits

Our client offers a competitive salary, a comprehensive benefits package including health insurance and retirement contributions, and excellent opportunities for professional development and career advancement. This role is based in Upington, Northern Cape , with a hybrid work model that combines field travel with flexibility. Join a leading pharmaceutical company that is dedicated to ethical research and employee growth. You will be part of a collaborative team working on life-changing therapies and contributing to significant advancements in medicine.