Job Summary
The SME-Pharmacovigilance role is crucial for ensuring the safety and efficacy of pharmaceutical products. The candidate will leverage their expertise in PV Case Processing and customer service to enhance pharmacovigilance operations. This position requires a proactive approach to monitoring drug safety and contributing to research and development efforts.
Responsibilities
· Triage & intake of ICSRs in ARGUS databases within agreed timelines
· Download and monitor valid ICSRs from Eudra Vigilance (EV)- or any other sources
· Process literature, spontaneous, clinical trial, and solicited cases
· Search for valid ICSRs in Literature search tools
· Generate reports and submit to health authorities and business partners
· Enter serious and non-serious ICSRs in ARGUS per client SOP and WI with high accuracy
· Code events, indications, patient history using MedDRA
· Code suspect products, amend narratives, and label events
· Obtain follow-up information for all cases per applicable guidelines
· Submit processed cases to regulatory authorities and distribute reports to Partners
· Communicate effectively with client stakeholders and internal teams
· Attend all internal and client trainings to ensure guideline compliance
· Ensure adherence to regulatory requirements and industry standards in all aspects of pharmacovigilance and safety operations.
· Assist in the development and maintenance of standard operating procedures to ensure consistency and quality in process execution.
· Support training and development initiatives to enhance team capabilities and knowledge in pharmacovigilance and safety operations.
· Utilize technical skills to troubleshoot and resolve process-related issues, minimizing disruptions and ensuring smooth operations.
· Engage in rotational shifts to provide consistent support and coverage across different time zones.
Requirements
· Bachelor’s / Master’s degree in pharmacy.
· Minimum 3 years relevant work experience in case processing activities.
· Experience in Cardiovascular (CVS), Neuroscience (CNS), Oncology, Immunology therapeutic areas and Gene Therapy will be an added advantage. Experience with global pharma sponsor will be preferred.
· In-depth knowledge and understanding of applicable global, regional, and local regulatory requirements, including Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and International Conference of Harmonization (ICH) guidelines, SOPs.
· Excellent organizational and time management skills.
· Proficiency in Microsoft Office and web-based applications (e.g., Word, Excel, PowerPoint).
· Good knowledge of medical terminology.
The Cognizant community:
We are a high caliber team who appreciate and support one another. Our people uphold an energetic, collaborative and inclusive workplace where everyone can thrive.
- Cognizant is a global community with more than 300,000+ associates around the world.
- We don’t just dream of a better way – we make it happen.
- We take care of our people, clients, company, communities and climate by doing what’s right.
- We foster an innovative environment where you can build the career path that’s right for you.
About us:
Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2024) is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at www.cognizant.com
Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
If you have a disability that requires reasonable accommodation to search for a job opening or submit an application, please email [email protected] with your request and contact information.
Disclaimer:
Compensation information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.
Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.