Clinical Research Associate Job Vacancy in Samfya, Zambia – Healthcare

Job Description

Position: Clinical Research Associate

Company: Pfizer Zambia

Location: Samfya, Zambia

Experience: 3-5 years of experience in clinical research, preferably in pharmaceutical trials

Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing or related field

Employment Type: Full-time

Industry: Healthcare

Department: Research & Development

Salary: SSP 30,000 – 45,000 per month

Vacancies:1

Company Overview

Pfizer Zambia is a leading global pharmaceutical company dedicated to improving health outcomes across the continent. With a strong presence in Zambia, Pfizer focuses on delivering innovative medicines, vaccines, and health solutions that address the most pressing medical needs of the population. The Samfya office serves as a strategic hub for clinical operations, supporting trials that span multiple therapeutic areas, including oncology, infectious diseases, and cardiovascular health. Pfizer’s commitment to ethical research, patient safety, and community engagement makes it an employer of choice for professionals seeking to make a meaningful impact in the healthcare sector.

As part of its mission to advance science and improve lives, Pfizer Zambia collaborates with local hospitals, research institutions, and regulatory bodies to ensure that clinical studies meet the highest standards of quality and compliance. The company invests heavily in employee development, offering continuous training, mentorship programs, and opportunities for career progression within a dynamic, multicultural environment.

Job Overview

The Clinical Research Associate (CRA) will play a pivotal role in the planning, execution, and monitoring of clinical trials conducted in Zambia. Reporting to the Clinical Operations Manager, the CRA will ensure that studies are conducted in accordance with the protocol, Good Clinical Practice (GCP), and all applicable regulatory requirements. This position offers a unique opportunity to contribute to groundbreaking research that can transform patient care across the region.

For more information about our career opportunities, visit our main portal: https://zambiajobssearch.com

Explore related opportunities in neighboring markets: https://zimbabwejobsearch.com/

Discover additional regional openings: https://mozambiquejobsearch.com/

Key Responsibilities

• Coordinate and monitor all aspects of clinical trial activities at study sites in Samfya and surrounding regions.
• Ensure compliance with study protocols, GCP guidelines, and local regulatory requirements.
• Conduct site initiation visits, routine monitoring visits, and close‑out visits, documenting findings accurately.
• Manage source data verification, query resolution, and timely reporting of adverse events.
• Collaborate with investigators, study coordinators, and internal cross‑functional teams to resolve issues and optimize study performance.
• Maintain comprehensive trial documentation, including regulatory binders, case report forms, and electronic data capture systems.
• Assist in the preparation of study reports, regulatory submissions, and audit readiness activities.

Required Skills

• Strong knowledge of GCP, ICH guidelines, and local regulatory frameworks.
• Excellent communication and interpersonal skills for effective stakeholder engagement.
• Proficiency in electronic data capture (EDC) systems and clinical trial management software.
• Detail‑oriented with strong organizational and time‑management abilities.
• Ability to travel to multiple sites within the region as required.
• Problem‑solving mindset with a proactive approach to issue resolution.

Education

A minimum of a Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related discipline is required. Advanced certifications such as Certified Clinical Research Professional (CCRP) or equivalent are advantageous.

Experience

Applicants should possess 3‑5 years of hands‑on experience as a Clinical Research Associate or in a similar role within the pharmaceutical industry. Experience conducting trials in low‑resource settings or emerging markets is highly valued.

Salary

The position offers a competitive salary range of SSP 30,000 to 45,000 per month, commensurate with experience and qualifications. Additional performance‑based incentives may be provided.

Benefits

• Comprehensive health insurance covering medical, dental, and vision.
• Retirement savings plan with employer contributions.
• Paid annual leave, sick leave, and public holidays.
• Professional development allowance for certifications and conferences.
• Employee assistance program and wellness initiatives.

Training

• On‑boarding program covering Pfizer’s SOPs, GCP, and local regulatory landscape.
• Continuous training modules on advanced clinical monitoring techniques.
• Mentorship from senior clinical operations leaders.
• Access to Pfizer’s global learning platform for skill enhancement.

Working Environment

Pfizer Zambia offers a collaborative, inclusive, and safety‑focused workplace. The Samfya office provides modern facilities, flexible working arrangements, and a culture that encourages innovation and knowledge sharing. Employees benefit from a supportive leadership team that values diversity, equity, and professional growth.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online application portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for a virtual interview followed by an on‑site assessment.

Equal Opportunity Statement

Pfizer Zambia is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, race, religion, disability, or sexual orientation. Our recruitment practices are designed to ensure fairness and transparency, providing all qualified applicants with an equal chance to succeed.