Clinical Research Associate Job Vacancy in Bamenda, Cameroon – Pharmaceuticals

Job Description

Position: Clinical Research Associate

Company: Novartis AG

Location: Bamenda, Cameroon

Experience: 3-5 years

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

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Clinical Research

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

Vacancies:1

Company Overview

Novartis AG is a global leader in innovative medicines, dedicated to improving health outcomes worldwide. With a strong presence in Africa, Novartis brings cutting‑edge research, development, and manufacturing capabilities to Cameroon, supporting local healthcare infrastructure and fostering scientific excellence. As part of its commitment to the region, Novartis invests in community health programs, partnerships with local universities, and sustainable practices that align with the country’s development goals. This dynamic environment offers unparalleled Career Opportunities in Cameroon for professionals eager to make a meaningful impact in the pharmaceutical sector.

Job Overview

The Clinical Research Associate (CRA) will play a pivotal role in managing and monitoring clinical trials conducted in Cameroon, ensuring compliance with regulatory standards and study protocols. Reporting to the Clinical Project Manager, the CRA will coordinate with investigators, sites, and internal teams to facilitate high‑quality data collection and patient safety. This position is essential for advancing Novartis’ pipeline of innovative therapies and contributes directly to the company’s mission of delivering life‑changing medicines. For more information about Novartis and its global initiatives, visit https://cameroonjobsearch.com/.

Key Responsibilities

• Monitor clinical trial sites in Bamenda and surrounding regions to ensure adherence to protocol, Good Clinical Practice (GCP), and regulatory requirements.
• Conduct site initiation, routine monitoring, and close‑out visits, preparing detailed reports and corrective action plans.
• Collaborate with investigators, study coordinators, and ethics committees to facilitate patient recruitment and informed consent processes.
• Verify source data, ensure accurate case report form (CRF) completion, and resolve data queries promptly.
• Maintain comprehensive trial documentation, including regulatory submissions, safety reports, and audit readiness files.
• Support the preparation of study timelines, budgets, and risk assessments.
• Participate in internal project meetings, providing updates on site performance and potential issues.
• Assist in the development and implementation of training materials for site staff.

Required Skills

• Strong knowledge of GCP, ICH guidelines, and local regulatory frameworks.
• Excellent communication and interpersonal skills for effective stakeholder engagement.
• Proficiency in electronic data capture (EDC) systems and Microsoft Office Suite.
• Analytical mindset with attention to detail and problem‑solving abilities.
• Ability to travel frequently within the region and manage multiple site visits.
• Fluency in English and French is essential.

Education

A minimum of a Bachelor’s degree in Pharmacy, Nursing, Life Sciences, or a related discipline is required. Advanced degrees (e.g., MSc, MPH) or certifications such as Certified Clinical Research Professional (CCRP) are advantageous.

Experience

Applicants should have 3‑5 years of experience in clinical monitoring or related roles within the pharmaceutical industry, preferably with exposure to trials conducted in Africa.

Salary

The compensation package ranges from 2,500,000 to 3,500,000 SSP per month, reflecting the candidate’s expertise and the responsibilities of the role. This competitive salary aligns with market standards for similar positions in Cameroon.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan with employer contributions.
• Performance‑based bonuses and annual salary reviews.
• Paid parental and sick leave in accordance with Cameroonian labor law.
• Professional development allowance for conferences and certifications.

Training

• On‑boarding program covering Novartis’ SOPs, GCP, and local regulatory requirements.
• Continuous learning opportunities through internal e‑learning platforms.
• Mentorship from senior clinical research professionals.
• Access to global webinars and workshops on emerging therapeutic areas.

Working Environment

Novartis offers a collaborative, inclusive, and innovative workplace where diversity is celebrated. Employees benefit from modern office facilities in Bamenda, flexible working arrangements, and a culture that encourages knowledge sharing and career growth. The role involves both office‑based tasks and field visits, providing a balanced and dynamic work experience.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on our website. Applications will be reviewed on a rolling basis, and shortlisted applicants will be contacted for a virtual interview followed by on‑site assessments.

Equal Opportunity Statement

Novartis AG is an equal opportunity employer. We welcome applications from all qualified individuals regardless of gender, race, religion, disability, or any other protected characteristic. Our commitment to diversity and inclusion ensures a supportive environment for all employees.