Clinical Research Associate Job Vacancy in Chililabombwe, Zambia – Pharmaceuticals

Job Description

Position: Clinical Research Associate

Company: Pfizer Zambia

Location: Chililabombwe, Zambia

Experience: 2-4 years of clinical research experience

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

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Clinical Operations

Salary: SSP 150,000 – 250,000 per month

Vacancies:1

Company Overview

Pfizer is a global leader in innovative medicines, vaccines, and consumer health products. With a strong presence in Zambia, Pfizer Zambia is dedicated to improving health outcomes through cutting‑edge research, local partnerships, and community outreach. The company operates state‑of‑the‑art facilities and collaborates with hospitals, universities, and regulatory bodies to bring life‑saving therapies to patients across the nation.

As part of its commitment to excellence, Pfizer Zambia invests heavily in talent development, fostering a culture of scientific curiosity, integrity, and collaboration. Employees enjoy a supportive environment that encourages continuous learning, professional growth, and meaningful impact on public health. This makes Pfizer Zambia a premier destination for ambitious professionals seeking to advance their careers in the pharmaceutical sector.

Joining Pfizer Zambia means becoming part of a worldwide network of experts while contributing directly to the health and wellbeing of Zambians. The role offers exposure to international best practices, robust training programs, and the chance to work on groundbreaking clinical studies that shape the future of medicine.

Job Overview

The Clinical Research Associate (CRA) will support 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 compliance with Good Clinical Practice (GCP), local regulations, and Pfizer’s internal standards. This position plays a critical role in safeguarding participant safety, data integrity, and study timelines, thereby contributing to the successful delivery of new therapies.

For more information about Pfizer Zambia and its commitment to innovation, visit https://zambiajobssearch.com/. This opportunity is a key part of our ongoing hiring in Zambia, offering career opportunities in a dynamic, fast‑growing environment.

Key Responsibilities

• Coordinate site selection, initiation, monitoring, and close‑out activities for assigned clinical trials.
• Ensure compliance with protocol, GCP, and local regulatory requirements at each study site.
• Conduct source data verification, query resolution, and accurate documentation of trial data.
• Maintain effective communication with investigators, site staff, and internal project teams.
• Prepare and review regulatory submissions, informed consent forms, and study-related documentation.
• Identify and mitigate risks to study timelines and data quality.
• Participate in internal audits and contribute to continuous improvement initiatives.

Required Skills

• Strong knowledge of GCP, ICH guidelines, and local regulatory frameworks.
• Excellent organizational and time‑management abilities.
• Effective communication and interpersonal skills for stakeholder engagement.
• Proficiency in electronic data capture (EDC) systems and Microsoft Office Suite.
• Analytical mindset with attention to detail and problem‑solving capabilities.
• Ability to travel to multiple sites across Zambia as required.

Education

Candidates must hold a Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related discipline. Advanced degrees (e.g., MSc, PhD) or certifications such as Certified Clinical Research Professional (CCRP) are advantageous but not mandatory.

Experience

A minimum of 2‑4 years of hands‑on experience in clinical research monitoring, preferably within pharmaceutical or contract research organizations, is required. Experience with oncology, infectious diseases, or vaccine trials is a plus.

Salary

The position offers a competitive salary ranging from SSP 150,000 to SSP 250,000 per month, commensurate with experience and qualifications. Additional performance‑based incentives may be provided.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan with employer contributions.
• Generous paid leave, including annual, sick, and parental leave.
• Professional development allowance for conferences and certifications.
• Employee assistance program and wellness initiatives.
• Transportation allowance for site visits.

Training

• Induction program covering Pfizer’s culture, policies, and compliance standards.
• GCP and regulatory affairs training modules.
• On‑the‑job mentorship with senior clinical scientists.
• Access to online learning platforms for continuous skill enhancement.
• Opportunities to attend international webinars and scientific symposia.

Working Environment

Pfizer Zambia provides a collaborative, inclusive, and safety‑focused workplace. Employees work in modern office spaces equipped with the latest technology, and fieldwork involves visits to well‑equipped clinical sites across the country. The company promotes work‑life balance, encouraging flexible scheduling where operationally feasible.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their suitability for the role through the online portal on our website. 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, age, disability, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.