Manager Pharmacovigilance

7 - 11 years

0 Lacs

Posted:2 days ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

As a Pharmacovigilance professional at Clarivate, you will be responsible for performing pharmacovigilance services such as biomedical literature monitoring and assessing adverse events reporting. Your role will involve indexing and abstracting using your broad knowledge of scientific terms, medical terminology, drugs, and therapeutic areas, as well as pharmacovigilance regulations. **Key Responsibilities:** - Establish best practices and SOPs for literature screening activities, ensuring compliance with regulatory requirements and industry standards. - Oversee and coordinate all literature screening activities with a focus on quality and accuracy. - Ensure effective communication of findings to stakeholders and collaborate with cross-functional teams for safety updates and risk management. - Collaborate with cross-functional teams to develop and implement risk mitigation measures. - Set clear goals aligned with departmental and organizational objectives and lead the creation of a training program for new recruits. - Assess the performance of trainees and maintain training records ready for audit. **Qualifications Required:** - Bachelor's degree or equivalent in Pharmacy, Life Sciences, Nursing, or related field. - Minimum 7 years of relevant experience in drug safety/pharmacovigilance. - Experience with commercial and client-specific biomedical literature databases. - Writing skills to create succinct, accurate summaries and working knowledge of biomedical terminology, drugs, and therapeutic areas. It would be beneficial if you also possess: - Certification from a professional medical writers association. - Effective time management skills. - Excellent English written and verbal communication skills. - Adherence to SOP and policies. As part of the Pharmacovigilance team at Clarivate, you will provide services to global customers covering various therapeutic areas. You will work in a supportive environment with personalized training and opportunities to engage in different aspects of pharmacovigilance and customer engagement. The team is based in India (Bangalore or Noida) and operates from 9:00 AM IST to 6:00 PM IST or 11:00 AM to 8:00 PM (Mon-Friday) with a hybrid work mode. Clarivate is committed to offering equal employment opportunities to all qualified individuals regarding hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. Compliance with non-discrimination laws and regulations is maintained in all locations.,

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Clarivate

Information Services

London Penang

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