Senior Specialist Case Processing PharmaLex

3.0 - 7.0 years

0 Lacs

noida, uttar pradesh

On-site

As a member of the team at Cencora, you play a crucial role in creating healthier futures for people and animals everywhere. Your work is essential in delivering on our purpose of making a positive impact at the center of health. If you are passionate about improving lives and making a difference, we invite you to join our innovative company. **Role Overview:** - Perform triage and review for initial validity assessment of cases, including spontaneous, health authority, Clinical Trial, and literature cases. - Enter data into the PV database. - Assess initial ICSR, if applicable. - Evaluate the need for expedited reporting to Health Authorities/partners of a client, including reporting timeli...

Posted 3 weeks ago

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Senior Specialist Case Processing World Courier

2.0 - 5.0 years

3 - 12 Lacs

noida, uttar pradesh, india

On-site

Performing triage and review for initial validity assessment of cases including spontaneous, health authority, Clinical Trial and literature cases. Data entry into PV database Initial ICSR assessment, if applicable Evaluation of the need for expedited reporting to Health Authorities / partners of a client concerned, including reporting timelines Preparation of standard reporting forms (e.g., CIOMS I / MedWatch Forms and XML Preparation and sending of follow up requests Submission of ICSRs to Health Authorities and partners of a client Case completion / documentation Conduct quality checks of Individual Case Safety Reports (ICSRs) and ensure quality assurance in accordance with project requir...

Posted 2 months ago

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Senior Specialist Case Processing PharmaLex

5.0 - 9.0 years

0 Lacs

noida, uttar pradesh

On-site

As a member of the team at Cencora, you will play a crucial role in creating healthier futures for people and animals everywhere. Your responsibilities will include: - Performing triage and review for initial validity assessment of cases, such as spontaneous, health authority, Clinical Trial, and literature cases. - Data entry into the PV database. - Conducting initial ICSR assessment, when applicable. - Evaluating the need for expedited reporting to Health Authorities or partners of a client, including reporting timelines. - Preparing standard reporting forms like CIOMS I/MedWatch Forms and XML files. - Sending follow-up requests and submitting ICSRs to Health Authorities and partners of a ...

Posted 3 months ago

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