Clinical Safety Associate
3 weeks ago
Clinical Safety Associate
to join our dynamic team to contribute to the activities performed in the Hub:
Responsibilities: Processing of Adverse Events (AEs) / Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs), and other immediately reportable events in the safety database including relevant communication with Customer Query preparation, sending and follow-up Maintenance of study trackers and other relevant tools Reconciliation of clinical safety information/activities with Customer/CRO/Data Management Assisting in aggregate periodic safety reports preparation Assisting in expedited and periodic safety reports submissions
Education and Experience: BSc or equivalent in Life Science discipline or PharmD Experience in Pharmacovigilance/Drug Safety Data Entry Knowledge of databases (Safety database: SafetyEasy ) Knowledge of drugs and pharmaceutical environment Knowledge of
Pharmacovigilance/Drug Safety regulation
(national and international) and Pharmacovigilance tools Demonstrable case management experience Skills: Adaptability Analytical skills Flexibility Reliable Good writing skills Adept in using MS Office tools and Pharmacovigilance tools
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Delhi, Delhi, India DAVA Oncology Full timeClinical Research Associate – Tuberculosis InitiativeThis role offers an opportunity to contribute to a healthcare initiative aimed at improving access totuberculosis treatment, diagnostics, and patient care . The focus is on collaborating withleading hospitals and government TB treatment centersto enhance treatment delivery and optimize patient...
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