Founded in 1968, Lupin has established itself as a leader in the pharmaceutical industry, renowned for innovation, research excellence, and a commitment to healthcare. With a strong presence in over 100 countries, Lupin continues to deliver quality products that improve lives worldwide.
Responsibilities of a Clinical Trial Assistant
As a Clinical Trial Assistant at Lupin, you will be responsible for:
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- Document Management and Coordination:
- Preparing and sending Ethics Committee (EC) and Site Initiation Visit (SIV) dossiers to sites based on instructions from the COM/CPM/CRA.
- Maintaining and updating study trackers, including documents, finances, and study equipment.
- Clinical Trial Support:
- Dispatching clinical trial supplies to sites according to study requirements.
- Coordinating with study sites and assisting CRAs with in-house file updates and quality reviews.
- Reviewing invoices from sites and conveying feedback to CRAs and site teams.
- Meeting and Communication:
- Preparing minutes for important study-related discussions.
- Assisting training coordinators with organizing departmental training sessions.
- Administrative Assistance:
- Providing in-house support to CRAs for ongoing studies.
- Completing other assigned activities as per the study and organizational requirements.
Preferred Candidate Profile
Educational and Professional Background:
- Experience in Pharma, Biotech, or CROs in clinical research (0-3 years preferred).
Skills and Expertise:
- Thorough understanding of ICH-GCP guidelines.
- Strong communication skills, both written and verbal.
- Ability to multitask and work efficiently under pressure.
- Detail-oriented with the ability to work independently.
