Pharmacovigilance Specialist at ICON plc

Chennai, tamil nadu, India -

Full Time

Start Date

Immediate

Expiry Date

01 Aug, 26

Salary

0.0

Posted On

03 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Drug safety, Adverse event reporting, Regulatory compliance, Risk assessment, Signal detection, Data analysis, Clinical research, Regulatory submissions, Safety reporting, Communication, Interpersonal skills, Quality assurance

Industry

Biotechnology Research

Description

Pharmacovigilance Specialist 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 Specialist to join our diverse and dynamic team. As a Pharmacovigilance Specialist at ICON, you will be responsible for monitoring the safety of pharmaceutical products by analyzing, interpreting, and reporting adverse event data in accordance with regulatory requirements. Your expertise will play a critical role in ensuring patient safety and maintaining compliance with industry standards. What You Will Be Doing: Collecting, reviewing, and analyzing adverse event reports to ensure timely and accurate reporting in compliance with regulatory guidelines. Conducting risk assessments and signal detection activities to identify and evaluate potential safety concerns. Collaborating with cross-functional teams to support safety-related inquiries and investigations. Preparing and submitting safety reports and regulatory submissions in a timely manner. Staying current on pharmacovigilance regulations and industry best practices to enhance the safety framework. Your Profile: 6+ years experience in pharmacovigilance, drug safety, preferably within a clinical or pharmaceutical setting. Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. Strong analytical skills and attention to detail in data collection and reporting. Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams. A commitment to upholding high standards of quality and compliance in all pharmacovigilance activities. 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 Specialist is responsible for monitoring pharmaceutical product safety by analyzing and reporting adverse event data in compliance with regulatory standards. They will also conduct risk assessments, perform signal detection, and collaborate with cross-functional teams to support safety investigations.