Pharmacovigilance Project Lead at ICON plc

Chennai, tamil nadu, India -

Full Time

Start Date

Immediate

Expiry Date

10 Jan, 26

Salary

0.0

Posted On

12 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Drug Safety, Project Management, Safety Monitoring, Regulatory Compliance, Cross-Functional Coordination, Adverse Event Reporting, Analytical Skills, Problem-Solving, Communication Skills, Interpersonal Skills, Team Leadership, Training, Mentoring, Data Integrity, Patient Safety

Industry

Biotechnology Research

Description

Pharmacovigilance Project Lead ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Pharmacovigilance Project Lead to join our diverse and dynamic team. 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. You will ensure compliance with regulatory requirements, lead pharmacovigilance projects, and drive initiatives to enhance patient safety and data integrity across all projects. What You Will Be Doing: 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: Bachelor’s degree in life sciences, pharmacy, or a related field; advanced degree or certification in pharmacovigilance is a plus. 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. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

Responsibilities

The Pharmacovigilance Project Lead will oversee the strategic management of safety monitoring and reporting for clinical trials and post-marketing activities. This role includes ensuring compliance with regulatory requirements and leading pharmacovigilance projects to enhance patient safety and data integrity.