Pharmacovigilance Project Lead

Beschreibung:

Pharmacovigilance Project Lead - solid pharmacovigilance and drug safety experience needed - 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.

As a Pharmacovigilance Project Lead at ICON, you will oversee the strategic management of safety monitoring and reporting for clinical trials and post-marketing activities.

What You Will Do:

You will oversee pharmacovigilance and drug safety workstreams, ensuring deliverables meet quality and timeline expectations.

Key responsibilities include:
* Leading and managing pharmacovigilance projects, including overseeing safety data collection, evaluation, and reporting processes.
* Developing and implementing strategies to ensure the effective management of adverse event reports and compliance with global regulatory standards.
* Coordinating with cross-functional teams, including clinical operations, regulatory affairs, and data management, to support project objectives and resolve safety-related issues.
* Ensuring the timely preparation and submission of safety reports, including periodic safety updates and risk assessments, to regulatory authorities and sponsors.
* Providing leadership and guidance to pharmacovigilance teams, including training and mentoring staff to support project success and compliance.

Your Profile:

You will have solid pharmacovigilance and drug safety experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:
* Bachelor's degree in a relevant scientific discipline or healthcare-related field
* Proven experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting and regulatory requirements.
* Strong leadership and project management skills, with experience overseeing complex pharmacovigilance projects and managing cross-functional teams.
* Excellent analytical and problem-solving abilities, with a track record of driving improvements in safety monitoring processes.
* Effective communication and interpersonal skills, with the ability to collaborate with diverse stakeholders and manage multiple priorities in a fast-paced environment.

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