Pharmacovigilance Reporting Associate
Chennai, Trivandrum
JR126918
Drug Safety ICON Full Service & Corporate Support Office Based
About the Role
Pharmacovigilance Reporting Associate – India, CHN/BGLR; Office based
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.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Responsibilities
- Submission of expedited Serious Adverse Event (SAE) reports, periodic reports, line listings, and applicable safety information to clients, regulatory authorities, ethics committees, investigators, third-party vendors, partners, and ICON personnel, if required & as agreed with client during study set-up, within project-specified timelines.
- Release of safety reporting intelligence for expedited and periodic reports, line listings, for regulatory authorities, ethics committees, and investigators within specified timelines in accordance with company procedures.
- Maintain a strong understanding of ICON’s safety reporting systems, processes, and conventions, as appropriate.
- Maintain a strong understanding of ICON Standard Operating Procedures (SOPs), Working Procedures (WPs), guidance documents, and manuals associated with safety reporting.
- Perform oversight of assigned projects ensuring all ICON, sponsor, and regulatory timeframes are met for the reporting of safety information or for the release of global safety reporting intelligence requirements.
- Operate in a lead capacity ensuring ownership and accountability of safety reporting activities or safety reporting intelligence on assigned projects.
- Ensure completion of all assigned project activities accurately and in accordance with ICON standards, regulatory requirements, and client contractual obligations.
- Serve as support to the Safety Reporting Group management in all aspects of departmental activities, including but not limited to quality and compliance metric review, finance tracking and oversight, project resource tracking, client engagement, training oversight, and CAPA oversight as designated.
- Collaborate with various parties such as project team members, client contacts, investigators, adverse event reporters, and third-party vendors as applicable. Build and maintain good relationships across functional units.
- Work within multiple databases. Maintenance of project information or Pharmacovigilance intelligence information with timely updates to the project or intelligence databases.
- Perform filing and quality control of documents submitted to the eTMF or agreed filing solution ensuring file readiness on assigned projects for audits or inspections.
- Prepare for and represent the department in audits and inspections as designated.
- Review regulatory and safety reporting intelligence to keep updated on current regulations, practices, procedures, and proposals as assigned.
- Coach and mentor less experienced associates in safety reporting or safety reporting intelligence activities and other work, as needed.
- Implement and coordinate routine project activities, including presentations at client or investigator meetings, responses to client, authorities, and other stakeholders; review of project requirements and maintenance activities; review, escalation of metrics; and budget considerations as assigned.
- Participate in client and internal meetings, representing the Safety Reporting department for the assigned projects, as designated.
- Maintain understanding of applicable therapeutic areas and disease states as required.
- Travel (approximately 10%) domestic and/or international, as required.
- Perform other activities as identified and requested by management.
Keywords: Pharmacovigilance Reporting Associate, ICON plc, Clinical Research Organization, Patient-Centered Care, Drug Development, Healthcare Intelligence. ICON plc Pharmacovigilance Reporting Associate Job Opening! Apply Now. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.
