Pharmacovigilance Specialist Job Vacancy in Tunis, Tunisia – Pharmaceuticals

Job Description

Position: Pharmacovigilance Specialist

Company: Pfizer

Location: Tunis, Tunisia

Experience: 3-5 years in pharmacovigilance or drug safety

Education: Bachelor’s degree in Pharmacy, Medicine, or related field; Master’s preferred

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Drug Safety

Salary: 3000 – 5000 SSP per month

Vacancies:1

Company Overview

Pfizer is a global leader in innovative medicines, vaccines, and consumer health products. With a strong presence in Tunisia, Pfizer is committed to improving health outcomes through cutting‑edge research, rigorous quality standards, and a culture that values scientific excellence. The Tunis office serves as a regional hub for regulatory affairs, clinical development, and market access across North Africa.

Operating in more than 150 countries, Pfizer invests heavily in employee development, offering a collaborative environment where professionals can contribute to life‑changing therapies. The company’s core values—Integrity, Excellence, Courage, and Respect—guide every decision, ensuring that each team member can make a meaningful impact on patient health.

Pfizer’s commitment to sustainability and community engagement is evident through numerous initiatives in Tunisia, including health education programs, partnerships with local universities, and support for public health campaigns. As part of the Pfizer family, you will join a diverse workforce dedicated to scientific advancement and societal well‑being.

Job Overview

The Pharmacovigilance Specialist will play a pivotal role in monitoring the safety profile of Pfizer’s pharmaceutical products marketed in Tunisia and the broader MENA region. You will be responsible for collecting, assessing, and reporting adverse event data in compliance with local and international regulations, ensuring that patients receive safe and effective treatments.

This position collaborates closely with cross‑functional teams, including Clinical Development, Regulatory Affairs, and Medical Affairs, to provide timely safety insights that inform risk management strategies. The role also involves interaction with health authorities, healthcare professionals, and external partners to maintain transparent communication regarding product safety.

For more information about our career portal, visit https://tunisiajobsearch.com.

Key Responsibilities

• Collect, evaluate, and document adverse event reports from healthcare professionals, patients, and literature sources.
• Prepare and submit Individual Case Safety Reports (ICSRs) to the Tunisian National Agency for the Safety of Medicines and Health Products (ANSM) and other relevant authorities.
• Conduct signal detection activities and risk assessments to identify emerging safety concerns.
• Collaborate with Clinical Development to provide safety input for ongoing trials and post‑marketing studies.
• Maintain and update the local safety database, ensuring data integrity and compliance with Good Pharmacovigilance Practices (GVP).
• Develop and deliver safety training sessions for internal stakeholders and external partners.
• Prepare periodic safety update reports (PSURs) and risk management plans (RMPs) for regulatory submissions.

Required Skills

• Strong analytical abilities with attention to detail and accuracy.
• Excellent written and verbal communication skills in French and English; Arabic is a plus.
• Proficiency in pharmacovigilance software (e.g., Argus, Arisg).
• Ability to interpret clinical data and medical literature.
• Knowledge of local and international regulatory requirements (e.g., ICH, EMA, FDA).
• Effective teamwork and stakeholder management capabilities.

Education

A minimum of a Bachelor’s degree in Pharmacy, Medicine, Pharmacology, or a related scientific discipline is required. A Master’s degree or professional certification in Pharmacovigilance (e.g., PVPO) is highly desirable.

Experience

Applicants should have 3‑5 years of hands‑on experience in drug safety, pharmacovigilance, or a related field within the pharmaceutical industry. Experience with regulatory submissions in Tunisia or the MENA region is an advantage.

Salary

The position offers a competitive salary range of 3000 – 5000 SSP per month, commensurate with experience and qualifications. Additional performance‑based incentives may be provided.

Benefits

• Comprehensive health insurance covering medical, dental, and vision.
• Retirement savings plan with employer contributions.
• Generous paid time off and public holiday schedule.
• Professional development budget for conferences, certifications, and training.
• Employee assistance program and wellness initiatives.

Training

• Onboarding program covering Pfizer’s safety processes, systems, and compliance standards.
• Continuous learning opportunities through internal e‑learning platforms and external workshops.
• Mentorship from senior pharmacovigilance experts.

Working Environment

Pfizer provides a modern office environment in the heart of Tunis, equipped with state‑of‑the‑art technology and collaborative workspaces. Flexible working arrangements, including remote work options, are available to support work‑life balance.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining relevant experience through our online portal. Applications will be reviewed on a rolling basis. For additional career resources, visit https://ghanajobsearch.com/job-vacancy-ghana/.

Equal Opportunity Statement

Pfizer is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, religion, disability, or sexual orientation. Learn more about our global commitment to diversity at https://zambiajobssearch.com/job-vacancy-zambia/.