5 Pharmacovigilance Manager jobs in the United Arab Emirates

Pharmacovigilance and medical information associates play a crucial role in ensuring the safety of pharmaceutical products.

Our ideal candidate will be responsible for monitoring and analyzing product safety profiles, validating deliverables from vigilance teams, and reviewing protocols to ensure compliance with regulatory requirements.

1. Monitor and analyze product safety profiles to identify potential risks
2. Validate deliverables from vigilance teams to ensure accuracy and completeness
3. Review protocols and procedures to ensure compliance with regulatory requirements
4. Develop and implement risk management plans to mitigate potential risks
5. Collaborate with cross-functional teams to ensure seamless integration of pharmacovigilance activities

To succeed in this role, you will need:

• Strong analytical and problem-solving skills
• Ability to work effectively in a team environment
• Excellent communication and interpersonal skills
• Proficiency in Microsoft Office and data analysis tools
• Knowledge of pharmacovigilance regulations and guidelines

We offer a competitive salary and benefits package, including:

• Opportunities for professional growth and development
• A dynamic and supportive work environment
• Recognition and rewards for outstanding performance
• A comprehensive benefits package, including health insurance and retirement plan

We are a global leader in the pharmaceutical industry, dedicated to improving human health through innovative research and development. Our values include a commitment to excellence, integrity, and collaboration.

Our Pharmacovigilance and Medical Information Team is seeking a highly skilled professional to support the surveillance of product safety profiles and ensure compliance with regulatory requirements.

• Validate vigilance reports from team members
• Continuously monitor and analyze product safety profiles, identifying potential risks and benefits
• Review and argue paragraphs related to product tolerance in clinical trial protocols, investigator brochures, and summary of product characteristics
• Verify the existence of local vigilance systems and update procedures as needed
• Draft risk management plans and ensure their dissemination across the organization
• Respond to all authority questions and ensure signal detection activities
• Analyze the impact of regulatory texts on our products
• Update procedures related to this activity and participate in due diligence

• Proven experience in pharmacovigilance or a related field
• Strong analytical and problem-solving skills
• Ability to work independently and as part of a team
• Excellent communication and writing skills
• Fluency in English (written and spoken)

• A dynamic and supportive work environment
• Ongoing training and development opportunities
• The chance to work on challenging projects and make a meaningful contribution to our organization

Pierre Fabre is a global leader in the dermo-cosmetics and pharmaceutical industries. The company has a strong presence in over 130 countries and employs around 10,000 people worldwide.

The Group's portfolio includes several medical franchises and international brands, with a focus on innovation and quality.

As part of the team, you will be responsible for ensuring the continued surveillance of product safety profiles in development and commercialized products.

Key responsibilities include:

• Validating vigilance deliverables
• Monitoring and analyzing product safety profiles and risk-benefit ratios from information collected globally
• Reviewing and arguing tolerance paragraphs in study protocols, investigator brochures, IMPDs, clinical trial reports, and AMM files
• Verifying the existence of local vigilance systems
• Drafting risk management plans and disseminating them to subsidiaries
• Preparing responses to regulatory inquiries
• Ensuring signal detection activities
• Analyzing the impact of regulatory texts
• Updating procedures related to this activity
• Participating in due diligence

Strong analytical and problem-solving skills

Excellent communication and collaboration skills

Ability to work independently and as part of a team

Proficiency in Microsoft Office Suite

Competitive salary and benefits package

Opportunities for professional growth and development

Collaborative and dynamic work environment

Our group is recognized as one of the World's Best Employers 2021 by Forbes.

We are committed to diversity and inclusion, and our offers are open to all without restriction.

We are seeking an experienced Drug Safety Coding Specialist with a strong background in pharmacovigilance terminology and regulatory coding standards.

• Perform accurate and consistent coding of adverse events, medical history, lab terms, and concomitant medications using MedDRA and WHO-DD.
• Review and validate terms in Individual Case Safety Reports (ICSRs) to ensure alignment with global PV standards.
• Perform recoding or dictionary version updates in compliance with regulatory requirements.
• Collaborate with case processors, medical reviewers, and data management teams to resolve coding discrepancies.
• Ensure compliance with ICH-GCP, GVP, and internal SOPs.
• Maintain and update code lists and contribute to coding conventions development.
• Support training of new team members on dictionary use and coding best practices.
• Participate in audits, inspections, and quality control checks related to coding.

• B.Pharm / M.Pharm / PharmD / MBBS / BDS / B.Sc. Life Sciences
• MedDRA coding training or pharmacovigilance certification is a plus
• Strong analytical and problem-solving skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team

Interested to apply can share CV or call/WhatsApp to