Job Summary
A company is looking for a Drug Specialist I to support safety data collection and follow-up for clinical trials and post-marketing activities.
Key Responsibilities
- Conduct follow-up calls and outreach to collect safety data
- Process and review adverse event reports from clinical trials and spontaneous sources
- Identify and query missing safety information
Required Qualifications
- Degree in Life Sciences, Nursing, Pharmacy, or related field
- Minimum 4 years of pharmacovigilance or safety experience
- Experience with telephonic outreach and safety databases
- Knowledge of MedDRA coding
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