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:Minimum 5 years in clinical data management, clinical research, or biostatistics within pharmaceutical, biotechnology, or CRO environments

Education:Bachelor’s degree in Biostatistics, Life Sciences, Computer Science, Nursing, Public Health, or related field. Master’s degree or professional certification in Clinical Data Management (e.g., CCDM) preferred.

Employment Type:Full-time

Industry:Healthcare Research & Clinical Data Management

Department:Clinical Research & Development

Vacancies:1

Company Overview

Pfizer Inc. is a premier global biopharmaceutical company with a 170-year legacy of innovation and a profound commitment to delivering breakthroughs that change patients’ lives. Our mission is clear: to apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety, and value in the discovery, development, and manufacturing of medicines for everyone, everywhere. Our portfolio includes vaccines, medicines, and some of the world’s best-known consumer healthcare products. In Gambia, our operations are pivotal to advancing clinical research in West Africa, contributing to vital public health initiatives and building local capacity in advanced healthcare research methodologies. We are dedicated to creating a diverse and inclusive workplace where every colleague can grow and contribute to our purpose.

Job Overview

We are seeking a meticulous and experienced Clinical Trial Data Manager to join our Clinical Research & Development team in Bwiam, Gambia. This role is central to the integrity and success of our clinical trials in the region. You will be responsible for the end-to-end data management activities for assigned clinical studies, ensuring the collection, processing, and validation of clinical data meet the highest standards of quality, accuracy, and compliance with regulatory requirements. This position offers a unique opportunity to contribute to groundbreaking medical research while developing expertise in global clinical data standards and systems. You will collaborate closely with cross-functional teams including Clinical Operations, Biostatistics, Medical Affairs, and Programming to ensure clean, reliable, and analysis-ready databases. For more Jobs in Gambia and Career Opportunities in Gambia, visit our partner portal. Explore this and other Job Vacancy in Gambia listings to find your next career move.

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Key Responsibilities

• Develop and review data management documentation including Data Management Plans (DMPs), Case Report Form (CRF) completion guidelines, and data validation specifications.
• Design and validate electronic Case Report Forms (eCRFs) using clinical data management systems (e.g., Medidata RAVE, Oracle Clinical).
• Perform user acceptance testing (UAT) for clinical databases and edit checks.
• Oversee the data collection process, including site training on data entry guidelines and electronic data capture (EDC) systems.
• Manage and perform clinical data cleaning activities, including running data validation checks, query generation, and resolution tracking.
• Perform medical coding (MedDRA and WHODrug) for adverse events and concomitant medications.
• Coordinate and lead data review meetings with the clinical study team to identify data trends and issues.
• Manage database lock and unlock activities, ensuring all data management activities are complete and documented.
• Ensure compliance with FDA, ICH-GCP, GDPR, and other relevant regulatory guidelines for data management.
• Contribute to the preparation of data for statistical analysis and regulatory submissions.
• Participate in the selection and oversight of Contract Research Organization (CRO) data management activities, as required.
• Support internal and external audit/inspection activities related to data management.

Required Skills

• Expert knowledge of clinical data management processes, standards (CDISC), and regulatory requirements (ICH-GCP).
• Proficiency with leading clinical data management systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and electronic data capture (EDC) technology.
• Strong understanding of medical terminology, clinical trial design, and phases of clinical development.
• Excellent analytical and problem-solving skills with a keen attention to detail.
• Advanced skills in data review and reconciliation.
• Proven ability to manage multiple priorities and deliverables in a fast-paced, deadline-driven environment.
• Strong communication and interpersonal skills for effective collaboration with global and local teams.
• Leadership capabilities to guide and mentor junior data management staff.
• Fluency in English is required; knowledge of local languages is a significant advantage.

Education

A Bachelor’s degree in Biostatistics, Life Sciences, Computer Science, Nursing, Public Health, or a closely related scientific field is required. A Master’s degree in Clinical Research, Epidemiology, or Data Science is highly desirable. Professional certification such as Certified Clinical Data Manager (CCDM) from the Society for Clinical Data Management (SCDM) is a strong plus. Continuous education in data standards (CDISC), regulatory updates, and new data management technologies is expected.

Experience

A minimum of 5 years of hands-on experience in clinical data management within the pharmaceutical, biotechnology, or Contract Research Organization (CRO) industry is essential. Candidates must have demonstrated experience with the full data management lifecycle from study start-up through database lock for Phase I-IV clinical trials. Experience working on studies in infectious diseases, vaccines, or non-communicable diseases relevant to the African context is highly preferred. Prior experience in a global/matrix organization and familiarity with risk-based monitoring approaches are significant assets.

Benefits

• Competitive salary and comprehensive benefits package aligned with international standards.
• Performance-based annual bonus and long-term incentive plans.
• Extensive health, dental, and vision insurance for employee and family.
• Generous paid time off, including vacation, sick leave, and public 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 global network.

Training

• Comprehensive onboarding program covering Pfizer systems, processes, and compliance standards.
• Specialized training in advanced clinical data management systems and CDISC standards.
• Regular workshops on ICH-GCP updates, data integrity, and regulatory submission requirements.
• Leadership and project management training for career advancement.
• Access to Pfizer’s global online learning portal with thousands of courses.

Working Environment

You will be based in our modern clinical research office in Bwiam, working within a collaborative, science-driven, and patient-focused team. The role involves a hybrid working model, combining office-based work with remote flexibility. You will interact regularly with a diverse global team via digital collaboration tools. The environment is fast-paced and requires adaptability, but it is also highly supportive, with a strong emphasis on work-life balance, innovation, and ethical conduct. We provide the tools and technology needed to perform at your best.

Application Process

Interested and qualified candidates are invited to submit their updated CV and a cover letter detailing their relevant experience and motivation for this role through the official Pfizer careers portal. The recruitment process will include an initial screening, technical assessment, and multiple interview rounds with the hiring manager and key stakeholders. Only shortlisted candidates will be contacted. We encourage all eligible applicants seeking Employment in Gambia in the healthcare research sector to apply. Discover more about Hiring in Gambia across various sectors through our regional partners.

https://sudanjobsearch.com/job-vacancy-in-sudan/

https://cameroonjobsearch.com/job-vacancy-in-cameroon/

Equal Opportunity Statement

Pfizer is an equal opportunity employer and is committed to providing a diverse, inclusive, and accessible work environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We comply with all applicable employment laws in Gambia and are dedicated to creating a workplace where every employee feels valued and empowered to contribute to our shared mission.