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Cognizant
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Associate Returnship Program

Associate Returnship Program

Cognizant

4 - 7 years

15 - 25 Lacs

mumbai

Posted:1 day ago| Platform:

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Skills Required

standard operating procedures development regulatory submissions data analysis pv program pharmacovigilance regulatory requirements excel providing training ops continuous improvement case processing collaboration safety reporting communication skills

Work Mode

Work from Office

Job Type

Full Time

Job Description

Job Summary

We are seeking an experienced professional for the role of TL-Pharmacovigilance with 6 to 9 years of experience. The ideal candidate will have expertise in Pharma Research & Development and proficiency in MS Excel. Experience in PV Case Processing and Pharmacovigilance & Safety Ops is a plus. The role involves a hybrid work model with rotational shifts.

Responsibilities

Oversee the pharmacovigilance activities to ensure compliance with regulatory requirements and company standards.
Provide expertise in Pharma Research & Development to enhance the quality and efficiency of safety operations.
Utilize MS Excel to analyze and report pharmacovigilance data accurately and efficiently.
Coordinate with cross-functional teams to ensure seamless integration of safety data into the overall drug development process.
Monitor and evaluate adverse event reports to identify potential safety signals and trends.
Ensure timely and accurate case processing in accordance with standard operating procedures.
Collaborate with global teams to harmonize pharmacovigilance practices and share best practices.
Develop and implement safety monitoring plans to proactively manage potential risks.
Conduct regular audits and assessments to ensure compliance with pharmacovigilance regulations.
Provide training and guidance to junior staff on pharmacovigilance processes and procedures.
Support the preparation of safety reports and regulatory submissions.
Engage in continuous improvement initiatives to enhance pharmacovigilance operations.
Maintain up-to-date knowledge of pharmacovigilance regulations and industry trends.

Qualifications

Demonstrate strong expertise in Pharma Research & Development with a focus on safety operations.
Exhibit proficiency in MS Excel for data analysis and reporting.
Possess experience in PV Case Processing and Pharmacovigilance & Safety Ops as a valuable asset.
Show ability to work effectively in a hybrid work model with rotational shifts.
Display excellent communication and collaboration skills to work with cross-functional teams.
Have a keen eye for detail and a proactive approach to identifying and managing risks.

Certifications Required

Certified Pharmacovigilance Professional (CPP) or equivalent certification preferred.

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Associate Returnship Program