ICON
Supervisor, Pharmacovigilance (Safety reporting)
Bulgaria · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerICON
- LocationBulgaria
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
Supervisor Pharmacovigilance - Poland or Bulgaria
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Supervisor, Pharmacovigilance to join our diverse and dynamic team. Within this position you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products. You will contribute to ensuring patient safety and regulatory compliance through effective management of pharmacovigilance activities, coordination with cross-functional teams, and maintaining the highest standards of safety reporting.
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What You Will Be Doing:
Supervising the day-to-day pharmacovigilance safety reporting operations, ensuring timely and accurate reporting to regulatory authorities.
Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.
Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.
Managing safety submissions workflow and submission to regulatory authorities.
Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety reporting.
Your Profile:
8+ years in pharmacovigilance or drug safety
Bachelor’s degree in life sciences, pharmacy, or a related field.
Team Management skills
Solid experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance.
Strong knowledge of global pharmacovigilance regulations and guidelines.
Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively.
Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked