Clinical Trials Project Coordinator Job Vacancy in Oshogbo, Nigeria – Pharmaceuticals – Clinical Research

Job Description

Position: Clinical Trials Project Coordinator

Company: Roche Nigeria

Location: Oshogbo, Nigeria

Experience: 2-4 years in clinical trial coordination or related field

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

Employment Type: Full-time

Industry: Pharmaceuticals – Clinical Research

Department: Clinical Operations

Salary: NGN 2,500,000 – NGN 3,500,000 per month

Vacancies:1

Company Overview

Roche Nigeria is a leading global healthcare company dedicated to improving patient outcomes through innovative medicines and diagnostics. With a strong presence across Africa, Roche combines cutting‑edge scientific research with a deep commitment to local communities. The company’s operations in Nigeria focus on delivering high‑quality pharmaceutical products, supporting clinical research initiatives, and fostering partnerships with hospitals, universities, and research institutions. As part of Roche’s worldwide network, the Oshogbo site plays a strategic role in expanding clinical trial capabilities in the southwestern region of the country, contributing to the broader mission of advancing health in Nigeria.

Roche’s reputation for scientific excellence and ethical standards makes it an attractive employer for professionals seeking meaningful career growth. The organization emphasizes a culture of collaboration, continuous learning, and diversity, ensuring that every employee can thrive while contributing to groundbreaking healthcare solutions. By joining Roche Nigeria, you become part of a global team that values innovation, integrity, and impact on the lives of patients across the continent.

Job Overview

The Clinical Trials Project Coordinator will support the planning, execution, and monitoring of Phase I‑III clinical studies conducted in Nigeria. Reporting to the Clinical Operations Manager, you will act as a liaison between internal project teams, external investigators, regulatory bodies, and CROs. This role is essential for ensuring that studies are conducted in compliance with Good Clinical Practice (GCP), local regulations, and Roche’s internal standards. The position offers a unique opportunity to contribute to life‑saving research while gaining exposure to international clinical development processes. For more information about Roche’s commitment to career development, visit https://nigeriajobsearch.com/.

Key Responsibilities

• Coordinate day‑to‑day activities of assigned clinical trials, including site initiation, monitoring visits, and close‑out procedures.
• Prepare and review essential trial documentation such as informed consent forms, case report forms, and regulatory submissions.
• Maintain accurate trial master files (TMF) and ensure timely updates in electronic data capture systems.
• Facilitate communication between study sites, CROs, and internal stakeholders to resolve operational issues.
• Track study timelines, budgets, and milestones, providing regular status reports to senior management.
• Assist in the preparation of safety reports, adverse event documentation, and audit readiness activities.
• Support the development and implementation of site training materials and ensure compliance with GCP guidelines.

Required Skills

• Strong organizational and multitasking abilities with keen attention to detail.
• Excellent written and verbal communication skills, capable of interacting with diverse stakeholders.
• Proficiency in clinical trial management systems (e.g., Medidata, Veeva) and Microsoft Office Suite.
• Knowledge of Nigerian regulatory requirements (NAFDAC) and international GCP standards.
• Problem‑solving mindset with the ability to anticipate and mitigate risks.
• Team‑oriented attitude with a collaborative approach to cross‑functional projects.

Education

A bachelor’s degree in Life Sciences, Pharmacy, Nursing, Biomedical Sciences, or a related field is required. Advanced certifications such as Certified Clinical Research Professional (CCRP) or equivalent are advantageous but not mandatory.

Experience

Applicants should have 2‑4 years of experience in clinical trial coordination, site management, or a related role within the pharmaceutical or CRO environment. Experience with multi‑site studies in Nigeria or other African countries is highly valued.

Salary

The compensation package ranges from NGN 2,500,000 to NGN 3,500,000 per month, commensurate with experience and qualifications. Salary is reviewed annually and includes 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 for certifications and conferences.
• Employee assistance program and wellness initiatives.

Training

• On‑boarding program covering Roche’s corporate culture, compliance, and clinical research processes.
• Access to internal e‑learning platforms for GCP, data management, and regulatory affairs.
• Mentorship from senior clinical scientists and project managers.
• Opportunities to attend international Roche training workshops and webinars.

Working Environment

Roche Nigeria offers a modern office environment in Oshogbo equipped with collaborative workspaces, meeting rooms, and secure data systems. The culture promotes work‑life balance, encouraging flexible working arrangements where feasible. Employees benefit from a supportive leadership team that values transparency, ethical conduct, and continuous improvement.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining relevant experience through the Roche Careers portal. Applications will be screened by the Talent Acquisition team, and shortlisted candidates will be invited for a virtual interview followed by an on‑site assessment at the Oshogbo office.

Equal Opportunity Statement

Roche Nigeria is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, ethnicity, disability, or any other protected characteristic. Our hiring practices reflect our dedication to fairness, and we encourage qualified individuals from all backgrounds to apply for this position.