Clinical Trial Assistant
51 minutes ago
**Key Responsibilities**:
- Assist in preparing and maintaining clinical trial documentation (e.g., study protocols, investigator brochures, informed consent forms).
- Support the coordination between clinical research sites and project teams.
- Track trial progress, including recruitment, data collection, and regulatory submissions.
- Ensure adherence to GCP (Good Clinical Practice) and SOPs.
- Assist in managing trial logistics, supplies, and data entry.
- Handle queries from stakeholders and assist in resolving issues promptly.
- Support audits and inspections by maintaining trial records and reports.
- Collaborate in cross-functional activities with clinical, regulatory, data management, and quality teams.
**Requirements**:
- Doctor of Pharmacy (Pharm.D) (mandatory).
- Freshers or up to 1-year experience in clinical research or healthcare industry preferred.
- Good understanding of clinical trial processes and documentation.
- Excellent communication and organizational skills.
- Ability to work independently and in a team environment.
- Proficiency in MS Office and data management tools.
- Attention to detail and adherence to protocols.
- Willingness to work in rotational shifts with flexibility.
- Commitment to a 2-year employment agreement.
**Note**:
**1. Need to do Cross functional, whenever other division/departments requires support**
**2. Need to agree with 2 year agreement**
**3. Should be okay with rotational shifts**
**Benefits**:
- Structured learning and growth opportunities.
- Exposure to real-time clinical trials and research processes.
- Friendly and collaborative work environment.
Pay: ₹17,000.00 - ₹22,000.00 per month
**Benefits**:
- Health insurance
- Provident Fund
Work Location: In person
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