Clinical Trial Data Manager Job Vacancy in Bwiam, Gambia – Healthcare Research & Clinical Data Management
Job Description
Position: Clinical Trial Data Manager
Company: Pfizer Inc.
Location: Bwiam, Gambia
Experience: 5+ years in clinical data management, clinical research, or biostatistics
Education: Bachelor’s degree in Biostatistics, Life Sciences, Computer Science, or related field; Master’s degree preferred
Employment Type: Full-time
Industry: Healthcare Research & Clinical Data Management
Department: Clinical Research & Development
Vacancies:1
Company Overview
Pfizer Inc. is a global biopharmaceutical company dedicated to discovering, developing, and delivering breakthrough medicines and vaccines that significantly improve patients’ lives. With a rich history of innovation spanning over 170 years, Pfizer operates in more than 125 countries, including a growing presence in The Gambia through its clinical research and public health initiatives. Our mission is to become the world’s most valued company to patients, customers, colleagues, investors, business partners, and the communities where we work and live. In The Gambia, Pfizer is committed to advancing healthcare research, building local capacity, and contributing to the development of robust clinical research infrastructure that can address both local and global health challenges. We believe in the power of science to transform lives and are dedicated to rigorous, ethical research that meets the highest standards of quality and integrity.
Job Overview
We are seeking a meticulous and experienced Clinical Trial Data Manager to join our clinical research team in Bwiam, Gambia. This role is central to the success of our clinical trials in the region, ensuring the accuracy, completeness, and integrity of all clinical trial data. The ideal candidate will be responsible for the end-to-end data management activities for assigned studies, from database design and validation through to database lock and archival. You will work closely with clinical research associates, biostatisticians, and medical monitors to ensure data quality and compliance with protocol, regulatory requirements, and standard operating procedures. This position offers a unique opportunity to contribute to groundbreaking medical research in a dynamic and collaborative environment, playing a key role in bringing new treatments to patients. For more Jobs in Gambia and Career Opportunities in Gambia, visit our partner site.
Key Responsibilities
- Develop and review data management plans (DMPs), data validation plans, and edit check specifications for clinical trials.
- Design, build, test, and validate clinical trial databases using electronic data capture (EDC) systems.
- Perform ongoing data review and cleaning activities, including query management and resolution with clinical sites.
- Ensure all data management activities comply with Good Clinical Practice (GCP), regulatory guidelines, and company SOPs.
- Coordinate and participate in database lock and unlock activities, ensuring data integrity is maintained.
- Generate and review data management metrics and status reports for study teams and management.
- Collaborate with biostatistics and programming teams to ensure timely and accurate data transfers for analysis.
- Manage and mentor junior data management staff or contractors as required.
- Contribute to the development and implementation of data management standards and best practices.
- Participate in the selection and oversight of vendors providing data management services.
Required Skills
- Expert knowledge of clinical data management processes, standards, and systems (e.g., Medidata Rave, Oracle Clinical, Veeva).
- Strong understanding of clinical research, GCP, ICH guidelines, and regulatory requirements for data management.
- Proficiency in database design, data validation, and data cleaning techniques.
- Excellent analytical and problem-solving skills with a keen attention to detail.
- Strong project management and organizational skills, with the ability to manage multiple priorities.
- Effective communication and interpersonal skills for collaborating with cross-functional and global teams.
- Ability to work independently and proactively in a fast-paced research environment.
- Familiarity with medical terminology, coding dictionaries (MedDRA, WHODrug), and CDISC standards is a plus.
Education
A Bachelor’s degree in Biostatistics, Life Sciences, Computer Science, Information Systems, or a related scientific field is required. A Master’s degree in a relevant discipline is highly preferred. Professional certifications in clinical data management (e.g., CCDM) are considered a strong asset. Continuous learning in data science, regulatory affairs, or clinical research is encouraged and supported.
Experience
A minimum of 5 years of direct experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry is required. Candidates must have hands-on experience with EDC systems and a proven track record of managing data for Phase II-III clinical trials from start-up to database lock. Experience working on studies in Africa or other emerging markets is a significant advantage. Prior experience in therapeutic areas relevant to Pfizer’s portfolio is desirable.
Benefits
- Competitive salary and comprehensive benefits package aligned with global standards.
- Performance-based annual bonus and long-term incentive plans.
- Extensive health, dental, and vision insurance for employees and their families.
- Generous paid time off, including vacation, sick leave, and company holidays.
- Retirement savings plan with company matching contributions.
- Continuous professional development opportunities, including access to global training programs and conferences.
- Support for further education and professional certification.
- Employee assistance programs and wellness initiatives.
- Opportunities for international career mobility within the Pfizer network.
Training
- Comprehensive onboarding program covering Pfizer’s systems, processes, and therapeutic areas.
- Ongoing training in advanced data management methodologies, new EDC technologies, and regulatory updates.
- Leadership and soft skills development programs for career advancement.
- Specialized training in therapeutic area knowledge relevant to assigned trials.
- Access to Pfizer’s global learning management system with thousands of online courses.
Working Environment
You will be based in our modern clinical research office in Bwiam, working within a collaborative, multidisciplinary team of dedicated professionals. The role may involve occasional travel to clinical trial sites within The Gambia or for regional meetings. Pfizer fosters an inclusive culture that values diversity, innovation, and a patient-centric approach. We provide the tools, technology, and support necessary to perform at your best and make a meaningful impact on global health.
Application Process
Interested candidates who meet the qualifications are invited to submit their application through the Pfizer careers portal. The process typically includes an initial resume screening, followed by one or more interviews with the hiring manager and team members. We encourage all qualified individuals to apply for this Job Vacancy in Gambia. Please ensure your application highlights your specific experience in clinical data management.
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Equal Opportunity Statement
Pfizer is an equal opportunity employer and is committed to providing a workplace free from discrimination and harassment. All qualified applicants will receive consideration for Employment in Gambia without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. We are proud of our diverse workforce and believe that inclusion drives innovation.
