Pharmacovigilance Specialist Job Vacancy in Louga, Senegal – Pharmaceuticals

Job Description

Position: Pharmacovigilance Specialist

Company: Sanofi Senegal

Location: Louga, Senegal

Experience: 3-5 years in drug safety or related field

Education: Bachelor’s degree in Pharmacy, Medicine, or Life Sciences (Master’s preferred)

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Pharmacovigilance

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

Vacancies:1

Company Overview

Sanofi is a global healthcare leader dedicated to improving lives through innovative medicines, vaccines, and consumer health solutions. Operating in Senegal for over a decade, Sanofi Senegal combines international expertise with local insight to address the health challenges of the West African region. The company’s commitment to scientific excellence, patient safety, and sustainable development makes it a premier employer for professionals seeking meaningful impact. By joining Sanofi, you become part of a diverse team that values collaboration, integrity, and continuous learning, contributing to the broader mission of advancing health outcomes across Senegal and beyond. This role offers a unique opportunity to work within a dynamic environment that supports career growth while delivering high‑quality pharmaceutical products to the market.

Job Overview

The Pharmacovigilance Specialist will be responsible for monitoring, assessing, and reporting adverse drug reactions (ADRs) to ensure the safety of Sanofi’s products in Senegal. You will collaborate with cross‑functional teams, healthcare professionals, and regulatory authorities to collect safety data, conduct signal detection, and implement risk management strategies. This position plays a critical role in safeguarding public health and maintaining compliance with national and international regulations. For more information about our career opportunities, visit Senegal Job Search, where you can explore additional roles and learn about our hiring process.

Key Responsibilities

• Collect, evaluate, and document adverse event reports from healthcare providers, patients, and internal sources.
• Perform case assessments, causality analysis, and seriousness classification in accordance with local regulations.
• Prepare and submit periodic safety update reports (PSURs) and individual case safety reports (ICSRs) to the Senegalese health authority.
• Collaborate with clinical, regulatory, and medical affairs teams to develop risk mitigation plans.
• Conduct signal detection activities and recommend appropriate follow‑up actions.
• Provide safety training and guidance to sales, marketing, and medical teams.
• Maintain up‑to‑date knowledge of pharmacovigilance guidelines, including ICH, WHO, and national requirements.
• Support audit readiness and contribute to internal and external inspections.

Required Skills

• Strong analytical and problem‑solving abilities with attention to detail.
• Excellent written and verbal communication skills in French and English.
• Proficiency in pharmacovigilance databases (e.g., Argus, VigiBase) and Microsoft Office suite.
• Ability to work independently and within multidisciplinary teams.
• Knowledge of regulatory frameworks governing drug safety in Senegal and the African region.
• High ethical standards and commitment to patient confidentiality.

Education

A minimum of a Bachelor’s degree in Pharmacy, Medicine, Pharmacology, or a related life‑science discipline is required. A Master’s degree or specialized training in pharmacovigilance, drug safety, or clinical research is highly desirable and will be considered an asset during the selection process.

Experience

Candidates should have three to five years of hands‑on experience in pharmacovigilance, drug safety, or clinical monitoring within a pharmaceutical or biotech environment. Experience with regulatory submissions, signal management, and safety data management in an African context will be viewed favorably.

Salary

The compensation package ranges from 1,200,000 to 1,800,000 SSP per month, commensurate with experience, qualifications, and performance. Salary reviews are conducted annually, and the role 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

• Onboarding program covering Sanofi’s safety processes and local regulatory requirements.
• Continuous training in pharmacovigilance best practices, data analytics, and risk management.
• Access to internal e‑learning platforms and external workshops.

Working Environment

Based in Louga, the role offers a modern office setting equipped with the latest technology to facilitate efficient data handling and collaboration. Sanofi promotes a culture of inclusion, where diverse perspectives are encouraged, and flexible working arrangements are considered to support work‑life balance.

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 screened by the Talent Acquisition team, followed by a technical interview and a final assessment with the hiring manager. Successful applicants will be notified within four weeks of submission.

Equal Opportunity Statement

Sanofi Senegal is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of gender, age, disability, ethnicity, religion, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.