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Job Description
Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. Qualification & Specifications :MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry). 2020 -2024 passed out
Skills Required:
- Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine.
- Attention to Detail: Meticulous accuracy in data entry and documentation.
- Analytical Skills: Ability to analyze data and identify safety signals.
- Regulatory Knowledge: Understanding of Good Pharmacovigilance Practices (GVP) and other regulations.
Key Responsibilities:
- Case Processing: Receive, document, and process reports of adverse drug reactions (ADRs) from various sources, ensuring accurate data entry into safety databases.
- Signal Detection: Analyze safety data to identify new risks or trends associated with a drug.
- Risk Management: Develop and implement strategies to mitigate identified risks, ensuring the drug's benefits outweigh its potential harms.
- Regulatory Reporting: Prepare and submit safety reports (e.g., PSURs) to regulatory authorities, ensuring compliance with global guidelines.
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- Documentation: Create and maintain accurate and compliant scientific and regulatory documents, including Standard Operating Procedures (SOPs) and safety reports.
For more details Contact
Vinodhini (HR)
7540052460
Mail to - contact@resolveitech.com
Skills
PharmacovigilanceMedical CodingCPTCPCRadiologyHccCpc CertifiedEDIf an employer asks you to pay any kind of fee, please notify us immediately. Jobaaj does not charge any fee from the applicants and we do not allow other companies also to do so.
Important dates & deadlines?
Application Deadline
11 Jan 26, 05:09 PM IST
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