Pharmacovigilance Associate
9 hours ago
Pharmacovigilance Associate
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 Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance.
What You Will Be Doing:
- Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.
- Conducting signal detection and risk assessment activities to identify potential safety issues.
- Collaborating with cross-functional teams to support safety-related inquiries and investigations.
- Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices.
- Assisting in the preparation of safety reports and regulatory submissions.
Your Profile:
- Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred.
- 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.
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.
-
Senior Pharmacovigilance Reporting Associate
5 days ago
Chennai, Tamil Nadu, India ICON plc Full time ₹ 9,00,000 - ₹ 12,00,000 per yearSenior Pharmacovigilance Reporting AssociateICON 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 developmentWe are currently seeking a Senior Pharmacovigilance...
-
Hiring Safety Associate
2 weeks ago
Chennai, India Pharmnova Full time**Qualifications and relevant experience**: - 1-4 years of experience in pharmacovigilance particularly in safety report processing and review-ICSR or literature review. - Graduated in pharmacy, dental, nursing or life sciences. **Skills and competency requirements**: - Acumen to retrieve safety information from reports. - Responsible for data entry of...
-
Safety Surveillance Associate
2 weeks ago
Chennai, Tamil Nadu, India Pfizer Full timeAbout the job Use Your Power for Purpose At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential...
-
Associate Safety Data Management Specialist
6 days ago
Chennai, India Pfizer Full timeThis job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety...
-
Associate Safety Data Management Specialist
7 hours ago
Chennai, Tamil Nadu, India Pfizer Full time ₹ 4,00,000 - ₹ 8,00,000 per yearIn this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database.Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database, prioritizing cases as per company guidance, updating...
-
Associate Safety Data Management Specialist
3 weeks ago
Chennai, India myGwork - LGBTQ+ Business Community Full timeJob Description This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the...
-
Safety Data Management Specialist
2 weeks ago
IND - Chennai Office, India Pfizer Ltd Full time ₹ 9,00,000 - ₹ 12,00,000 per yearAssociate Safety Data Management Specialist In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database. Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database,...
-
Safety Surveillance Associate
4 days ago
Chennai, India Pfizer Full timeWhy Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
-
Cloud Engineer – Microsoft Azure
6 days ago
Selaiyur, Chennai, Tamil Nadu, India Pharmnova Medical Research Pvt Ltd Full time ₹ 3,00,000 - ₹ 5,00,000 per yearJob SummaryWe are seeking a skilled and proactive Cloud Engineer with experience in Microsoft Azure and relevant domain knowledge in healthcare, pharmacovigilance (PV), or CRO environments. This role combines responsibilities across cloud infrastructure, on-premises IT systems, and IT support to ensure smooth and secure operations.Key ResponsibilitiesDesign,...
-
Aggregate Report Analyst Senior Associate
6 days ago
Chennai, India Pfizer Full timeThis job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Position Purpose The PSSR Aggregate Report Analyst creates documents pertaining to post-marketing safety data to support product development, license application, and...