Job Description
Position: Clinical Research Associate
Company: Pfizer Ethiopia
Location: Bahir Dar, Ethiopia
Experience: 2-4 years in clinical research
Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing or related field
Employment Type: Full-time
Industry: Pharmaceuticals – Research & Development
Department: Clinical Research
Salary: SSP 150,000 – 250,000 per month
Vacancies:1
Company Overview
Pfizer Ethiopia is a leading global pharmaceutical company dedicated to improving health outcomes through innovative medicines, vaccines, and consumer health products. With a strong presence across Africa, Pfizer Ethiopia operates state‑of‑the‑art laboratories and collaborates with local hospitals, universities, and research institutions to drive scientific advancement. The company’s commitment to ethical standards, patient safety, and community engagement makes it a premier employer for professionals seeking impactful careers in the pharmaceutical sector. As part of its expansion strategy, Pfizer Ethiopia is establishing a robust clinical research hub in Bahir Dar, creating new career opportunities and contributing to the region’s economic growth. This role offers a unique chance to be part of a dynamic team that shapes the future of healthcare in Ethiopia and supports the nation’s ambition to become a hub for clinical trials in East Africa.
Job Overview
The Clinical Research Associate (CRA) will support the planning, execution, and monitoring of clinical trials in accordance with Good Clinical Practice (GCP), local regulations, and Pfizer’s internal standards. Reporting to the Clinical Project Manager, the CRA will act as the primary liaison between the study sites, internal stakeholders, and external partners. This position plays a critical role in ensuring data integrity, participant safety, and timely study completion, directly contributing to Pfizer’s pipeline of life‑saving therapies. For more information about Pfizer Ethiopia’s career opportunities, visit Pfizer Ethiopia Careers.
Key Responsibilities
- Coordinate and monitor site activities for assigned clinical studies, ensuring compliance with protocol and regulatory requirements.
- Conduct site initiation, monitoring, and close‑out visits, preparing detailed visit reports and follow‑up actions.
- Verify source data, ensure accurate case report form (CRF) completion, and resolve data queries promptly.
- Maintain effective communication with investigators, study coordinators, and internal project teams.
- Assist in the preparation of regulatory submissions, safety reports, and study documentation.
- Track study timelines, enrollment targets, and budget expenditures, providing regular status updates.
- Identify and mitigate risks, escalating issues to the Project Manager as needed.
Required Skills
- Strong knowledge of GCP, ICH guidelines, and Ethiopian regulatory requirements.
- Excellent organizational and time‑management abilities.
- Effective written and verbal communication skills in English and Amharic.
- Proficiency with electronic data capture (EDC) systems and Microsoft Office Suite.
- Analytical mindset with attention to detail and problem‑solving capabilities.
- Ability to work independently and collaboratively in a multicultural environment.
Education
A minimum of a Bachelor’s degree in Pharmacy, Nursing, Biology, Chemistry, or a related life‑science discipline is required. Advanced degrees (MSc, PhD) or certifications such as Certified Clinical Research Professional (CCRP) are advantageous.
Experience
Applicants should have 2‑4 years of hands‑on experience in clinical research monitoring, preferably within pharmaceutical or contract research organizations. Experience with oncology, infectious diseases, or vaccine trials is a plus.
Salary
The position offers a competitive salary range of SSP 150,000 to 250,000 per month, commensurate with experience and qualifications, along with performance‑based incentives.
Benefits
- Comprehensive health insurance covering employee and dependents.
- Retirement savings plan with employer contributions.
- Paid annual leave, sick leave, and public holidays.
- Professional development allowance and tuition reimbursement.
- Employee assistance program and wellness initiatives.
Training
- Induction program covering Pfizer’s corporate culture, compliance, and SOPs.
- Ongoing GCP and regulatory training workshops.
- Mentorship from senior clinical scientists and project managers.
- Access to internal e‑learning platforms for continuous skill enhancement.
Working Environment
The role is based in a modern office in Bahir Dar with flexible working arrangements, including occasional remote work. The CRA will travel to study sites across Ethiopia, requiring a valid driver’s license and willingness to travel up to 30% of the time. Pfizer Ethiopia fosters an inclusive, collaborative, and innovative workplace where diversity of thought is celebrated.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on the Pfizer Ethiopia careers page. 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 Ethiopia is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, religion, disability, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.