Clinical Research Coordinator Job Vacancy in Lunsar, Sierra Leone – Healthcare

Job Description

Position: Clinical Research Coordinator

Company: Johnson & Johnson Sierra Leone

Location: Lunsar, Sierra Leone

Experience: 2-4 years of clinical research experience

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

Employment Type: Full-time

Industry: Healthcare

Department: Clinical Operations

Salary: SSP 800,000 – 1,200,000 per month

Vacancies:1

Company Overview

Johnson & Johnson Sierra Leone is a leading multinational healthcare company dedicated to improving health outcomes across the nation. With a strong presence in pharmaceuticals, medical devices, and consumer health products, the company supports a broad portfolio of initiatives that address local health challenges. As part of its commitment to innovation and community impact, Johnson & Johnson Sierra Leone invests heavily in research, development, and capacity building, creating a dynamic environment for professionals seeking meaningful career growth. The organization values diversity, integrity, and collaboration, fostering a culture where every employee can contribute to the mission of advancing health for all Sierra Leoneans. This role offers a unique opportunity to be part of a global leader while making a tangible difference in the local healthcare landscape.

Job Overview

The Clinical Research Coordinator will manage and oversee clinical trial activities at our Lunsar site, ensuring compliance with regulatory standards, study protocols, and ethical guidelines. This position serves as the primary liaison between investigators, sponsors, and regulatory bodies, coordinating patient recruitment, data collection, and documentation. The role is critical for the successful execution of clinical studies that drive innovative treatments and improve patient care. For more information about our commitment to career development, visit our main website: https://sierraleonejobsearch.com.

Key Responsibilities

• Coordinate all phases of clinical trials, from start‑up to close‑out, ensuring adherence to timelines and budgets.
• Maintain accurate and complete study documentation, including case report forms, source documents, and regulatory submissions.
• Facilitate patient screening, enrollment, and follow‑up, ensuring informed consent is obtained and recorded.
• Monitor study sites for compliance with Good Clinical Practice (GCP) and local regulatory requirements.
• Prepare and present progress reports to internal stakeholders and external sponsors.
• Manage investigational product accountability, storage, and dispensing according to protocol.
• Collaborate with cross‑functional teams, including data management, pharmacovigilance, and medical affairs.
• Assist in the preparation of audit and inspection readiness activities.

Required Skills

• Strong knowledge of GCP, ICH guidelines, and local regulatory frameworks.
• Excellent organizational and multitasking abilities.
• Effective communication skills for interacting with investigators, sponsors, and regulatory authorities.
• Proficiency in electronic data capture (EDC) systems and Microsoft Office Suite.
• Attention to detail and high level of accuracy in documentation.
• Problem‑solving mindset with the ability to anticipate and mitigate study challenges.

Education

A bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related discipline is required. Advanced certifications such as Certified Clinical Research Professional (CCRP) or equivalent are advantageous and demonstrate a commitment to professional excellence.

Experience

Candidates should possess 2‑4 years of hands‑on experience in clinical research coordination, preferably within a multinational pharmaceutical or medical device environment. Experience with Phase I‑III trials and familiarity with local ethics committees will be considered strong assets.

Salary

The competitive salary range for this position is SSP 800,000 to 1,200,000 per month, commensurate with experience and qualifications. Performance‑based incentives may also be offered.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan with employer contributions.
• Paid annual leave and sick leave.
• Professional development allowance for certifications and conferences.
• Employee assistance program supporting mental health and well‑being.

Training

• On‑boarding program covering company policies, GCP standards, and local regulatory requirements.
• Continuous training modules on advanced clinical trial methodologies.
• Mentorship opportunities with senior clinical scientists.

Working Environment

The role is based at our modern Lunsar facility, equipped with state‑of‑the‑art laboratories, secure data management systems, and collaborative workspaces. Employees enjoy a supportive atmosphere that encourages teamwork, innovation, and a balanced work‑life integration.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through our online portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews. For additional career resources, explore our regional partner sites: https://namibiajobsearch.com/job-vacancy-in-namibia/ and https://eritreajobsearch.com/job-vacancy-eritrea/.

Equal Opportunity Statement

Johnson & Johnson Sierra Leone is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, disability, religion, or sexual orientation. Our recruitment practices reflect our dedication to fairness and merit‑based selection.