7 Pharmacovigilance Services Jobs

Role Overview: As a Pharmacovigilance Services Senior Analyst at Accenture, you will be aligned with the Life Sciences R&D vertical, providing services across the entire life sciences enterprise. Your main focus will be on Clinical, Pharmacovigilance & Regulatory sub-offerings, assisting leading biopharma companies in improving outcomes by converging around the patient. Key Responsibilities: - Manage the Affiliate Mailbox, reconcile reports per process, and perform all written follow-up attempts for both Serious and Non-serious cases. - Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database following clie...

As a Pharmacovigilance Services Specialist at Accenture, you will be responsible for managing the Affiliate Mailbox, reconciling reports, and performing follow-up attempts for Serious and Non-serious cases. Additionally, you will create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database according to client guidelines and global regulatory requirements. Key Responsibilities: - Management of the Affiliate Mailbox, reconciliation of reports, and written follow-up attempts for Serious and Non-serious cases. - Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follo...

Role Overview: As a Pharmacovigilance Services Associate at Accenture, you will be aligned with the Life Sciences R&D vertical. Your responsibilities will include managing the Affiliate Mailbox, reconciling reports, performing follow-up attempts for both Serious and Non-serious cases, and working on case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database. You are expected to work in any shift and have MICC experience. Key Responsibilities: - Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts for Serious and Non-serious cases - Case identification, da...

As a Pharmacovigilance professional at Clarivate, you will be responsible for performing pharmacovigilance services such as biomedical literature monitoring and assessing adverse events reporting. Your role will involve indexing and abstracting using your broad knowledge of scientific terms, medical terminology, drugs, and therapeutic areas, as well as pharmacovigilance regulations. **Key Responsibilities:** - Establish best practices and SOPs for literature screening activities, ensuring compliance with regulatory requirements and industry standards. - Oversee and coordinate all literature screening activities with a focus on quality and accuracy. - Ensure effective communication of finding...

Role Overview: As a Pharmacovigilance Services Associate at Accenture, you will be aligned with the Life Sciences R&D vertical. Your responsibilities will include the management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts for both Serious and Non-serious cases. You will be involved in creating and managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. Key Responsibilities: - Management of the Affiliate Mailbox - Reconciliation of reports per process - Performance of all wri...

Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Japanese (JLPT N3/ N2). A background in Pharma

As a Pharmacovigilance Services Analyst at Accenture, you will be responsible for providing Pharmacovigilance & Drug Safety Surveillance services. With 2 to 5 years of experience and educational qualifications in Any Graduation/Bachelor of Pharmacy/Master of Pharmacy, you will play a key role in the management of the Affiliate Mailbox, reconciliation of reports, and performing follow-up attempts for both Serious and Non-serious cases. Your responsibilities will include case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and global regulatory requirements. In this position, you are expected to po...