1.0 - 5.0 years

0 Lacs

pune, maharashtra

On-site

As an individual responsible for assisting with Clinical Safety and/or PSS operations associated with products, your role will involve managing and processing expeditable adverse events, ensuring timely submission to clients and regulatory agencies if required. Your primary goal is to provide high-quality service to clients in a safe and cost-effective manner. It is essential for you to comply with legal requirements such as the Health and Safety at Work Act 1974, COSHH regulations 1989, and EC Directives 1992/3 as outlined in the Company's Health and Safety Manual. Key Responsibilities: - Assist in processing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs) by maintaining ...

Posted 17 hours ago

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Senior Specialist Case Processing, PER Cencora

3.0 - 7.0 years

0 Lacs

noida, uttar pradesh

On-site

As a valued member of our team at Cencora, you play a crucial role in our mission to create healthier futures for people and animals worldwide. Your contributions are essential to our ability to fulfill this purpose, and we invite you to be a part of our innovative company where you can make a real difference at the core of health. If you are passionate about improving lives and seeking a rewarding career, we encourage you to apply today. Your responsibilities will include: - Performing triage and review to assess the validity of cases, including spontaneous, health authority, Clinical Trial, and literature cases. - Entering data into the Pharmacovigilance (PV) database. - Conducting initial...

Posted 2 months ago

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Medical Data Reviewer : Life Science : 20 LPA : Apply Now Outpace Consulting Services

7.0 - 12.0 years

10 - 20 Lacs

Pune, Bengaluru, Mumbai (All Areas)

Work from Office

Hi We are looking to hire Medical Data Reviewer for our Client. Please go through the JD and Apply. Responsibilities: Review subject/ patient level data for accuracy, to identify any anomalies, trends in patient reported data Review and provide inputs ion design of eCRF Review investigation product dosing Review all reported Adverse Events (AEs), Concomitant Medication and medical Ensure that any out of range data/ anomaly is verified Review all laboratory data on study subjects Review data in the form of visualizations and identify potential issues of concern Training new team members Qualifications: Bachelor/ Masters degree or equivalent in Life sciences/ Alternative Medicine (preferred) E...

Posted 3 months ago

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