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5.0 - 9.0 years
0 Lacs
rajasthan
On-site
The Safety & PV Specialist position in Dalian at Syneos Health offers you the opportunity to be part of a leading biopharmaceutical solutions organization dedicated to accelerating customer success. At Syneos Health, we focus on translating clinical, medical affairs, and commercial insights into impactful outcomes that address the challenges of the modern market. Our Clinical Development approach places the customer and patient at the core of our operations. We are committed to simplifying and optimizing our processes to enhance both our ease of collaboration and our dedication to our mission of changing lives. Whether you choose to work with us through a Functional Service Provider partners...
Posted 2 months ago
5.0 - 9.0 years
0 Lacs
pune, maharashtra
On-site
As a Safety & PV Specialist I at Syneos Health, based in the Pune Office, you will play a crucial role in ensuring the safety and pharmacovigilance of our products. Your primary responsibility will be to enter information into PVG quality and tracking systems for the receipt and tracking of ICSRs. Additionally, you will assist in the processing of ICSRs according to SOPs and project-specific safety plans. In this role, you will triage ICSRs, evaluate the data for completeness and accuracy, and ensure regulatory reportability. You will enter data into the safety database, code events, medical history, concomitant medications, and tests, and compile complete narrative summaries. Your attention...
Posted 3 months ago
2.0 - 6.0 years
0 Lacs
pune, maharashtra
On-site
As a Safety & PV Specialist I-Japanese at Syneos Health in Pune Office, your primary responsibility will be to ensure accurate and timely processing of Individual Case Safety Reports (ICSRs) in compliance with Standard Operating Procedures (SOPs) and regulatory requirements. You will play a crucial role in maintaining safety tracking, performing data entry into safety databases, coding events and medical history, and compiling narrative summaries. Additionally, you will be involved in the validation and submission of xEVMPD product records, management of duplicate ICSRs, and activities related to SPOR / IDMP. Your role will also include conducting literature screening and review for safety, ...
Posted 3 months ago
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