Wanted Clinical ResearchTrainee- New Delhi

Resolve Medicode; New Delhi, Dadri; On-site; INR 4,00,000 - 8,00,000; Full time

Job summary

A pharmaceutical company in New Delhi is seeking professionals in clinical trials to monitor and assess drug safety. Candidates should possess relevant degrees and skills in data entry, analysis, and regulatory knowledge. The role includes case processing, risk management, and preparing safety reports. Interested applicants can contact Nandini at [e-mail].

Qualifications

• Degree in Pharmacy, Life Sciences, or Medicine required.
• Passed out in 2020 - 2024.

Responsibilities

• Receive, document, and process reports of adverse drug reactions (ADRs).
• Analyze safety data to identify risks or trends associated with a drug.
• Develop and implement strategies to mitigate identified risks.
• Prepare and submit safety reports to regulatory authorities.
• Create and maintain accurate scientific and regulatory documents.

Skills

Scientific Background

Attention to Detail

Analytical Skills

Regulatory Knowledge

Education

MBBS, BDS, BHMS, BAMS, BSMS, PHARMACY, B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology)

Job description

Overview

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, PHARMACY, B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology)
• 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.
• Documentation: Create and maintain accurate and compliant scientific and regulatory documents, including Standard Operating Procedures (SOPs) and safety reports.

For more details contact

Nandini (HR)

7708146649
Mail to- [e-mail]