Pharmacovigilance Specialist @ Clin Biosciences

Job Description

Roles and Responsibilities

• Data Collection and Management: Receive, catalog, and manage large volumes of adverse event reports. 
• Reporting: Report adverse events and safety concerns to regulatory authorities, ensuring compliance with local and international regulations. 
• Assessment and Analysis: Evaluate safety data, identify potential safety signals, and assess the benefit-risk profile of drugs. 
• Compliance: Ensure that reporting and assessment are complete and comply with current practices and company policies. 
• Documentation: Maintain accurate and complete documentation of all drug safety information. 
• Communication: Communicate with various stakeholders, including internal teams, clients, and regulatory authorities. 

Qualifications

• Bachelor's degree in a related field, such as pharmacy, nursing, or biology
• 0-2 years of experience in pharmacovigilance or a related field
• Strong analytical and problem-solving skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team

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Rs 0 - 50K PM Rs 50K - 1 LPA Rs 1.0 - 1.5 LPA Rs 1.5 - 2.0 LPA Rs 2.0 - 2.5 LPA Rs 2.5 - 3.0 LPA Rs 3.0 - 3.5 LPA Rs 3.5 - 4.0 LPA Rs 4.0 - 4.5 LPA Rs 4.5 - 5.0 LPA Rs 5 - 6 LPA Rs 6 - 7 LPA Rs 7 - 8 LPA Rs 8 - 9 LPA Rs 9 - 10 LPA Rs 10 - 12 LPA Rs 12 - 14 LPA Rs 14 - 16 LPA Rs 16 - 18 LPA Rs 18 - 20 LPA Rs 20 - 22 LPA Rs 22 - 24 LPA Rs 24 - 26 LPA Rs 26 - 28 LPA Rs 28 - 30 LPA Rs 30 - 32 LPA Rs 32 - 34 LPA Rs 34 - 36 LPA Rs 36 - 38 LPA Rs 38 - 40 LPA Rs 40 - 42 LPA Rs 42 - 44 LPA Rs 44 - 46 LPA Rs 46 - 48 LPA Rs 48 - 50 LPA Rs 50 - 75 LPA Rs 75 Lakh - 1C PA Rs 1 Crore+ PA

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Keyskills:   pharmacovigilance argus safety arisg drug safety