PV Associate Job at ICON |For Pharmacy Graduates Apply Now
ICON, a world-leading healthcare intelligence and clinical research organization, is seeking a PV/Sr Associate to join our team. In this pivotal role, you’ll contribute to our mission of shaping the future of clinical development by ensuring the accurate and timely processing of safety events. This position offers the opportunity to work on diverse projects and collaborate with a global team, all while upholding the highest standards of quality and compliance.
- Job Position: PV Associate/Sr Associate
- Location: Chennai, India (Office or Home)
- Job ID: JR127208
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment that drives innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. 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 a competitive salary, ICON offers a range of benefits designed to be competitive within each country, with a focus on well-being and work-life balance opportunities for you and your family.
PV Associate at ICON Job Description
This role involves reviewing and processing safety events (pre-marketing, post-marketing, medical device, and drug) and/or other medically related information, as assigned, in accordance with project-specific procedures. You will be responsible for collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.
PV Associate Job at ICON – Key Responsibilities
- Review and process safety events (pre-marketing, post-marketing, medical device, and drug) and/or other medically related information in accordance with assigned tasks and project-specific procedures.
- Review abstracts and full articles to identify safety information from literature sources for both pre- and post-marketed products.
- Generate data listings from the safety database and assume responsibility for the accuracy of the data.
- Complete adverse event follow-up in writing and/or by phone based on requirements for each Client.
- Provide input and review relevant safety tracking systems for accuracy and quality, and assist with maintaining project files.
- Perform a safety review of clinical and diagnostic data as part of case processing.
- Be responsible for the effective and efficient development of the Safety Management Plan, including the development of specific processes to assure consistency within the project.
- Support the creation of post-marketing safety activities, such as PSMF, RMP, and PBRER.
- Support the Qualified Person for Pharmacovigilance as required.
- Liaise with the investigational site, reporter, and/or Sponsor as necessary regarding safety issues.
- Liaise with the ICON Medical Monitor, project manager, and other relevant departments as needed.
PV Associate Job at ICON – Qualifications
- Bachelor’s degree in life sciences, pharmacy, or a related field; advanced degree preferred.
Experience and Skills
- Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment.
- Strong analytical skills with attention to detail in data collection and reporting.
- Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders.
- A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
Keywords: Pharmacovigilance, PV Associate, Sr PV Associate, Drug Safety, Clinical Research, Life Sciences, Regulatory Affairs, Medical Device Safety, Chennai jobs, ICON careers, Clinical Development.
