On-Site Research Assistant (Part-Time)
Company: ProPharma
Location: Kanpur
Job Type: Part-Time (24 hrs/week)
Contract: 1 Year (Extendable)
Experience: 0–3 Years
Qualification: Bachelor’s Degree or equivalent
Job Overview
The On-Site Research Assistant supports clinical trial activities at a hospital site by assisting in study coordination, data entry, and documentation while ensuring compliance with regulatory guidelines.
Key Responsibilities
Site Coordination
Act as a point of contact for site communications
Coordinate daily clinical trial activities
Patient & Study Support
Assist in pre-screening of study participants
Support ongoing clinical trial activities
Data Entry & Monitoring
Enter and manage clinical data in clinical databases
Evaluate and respond to system queries
Monitor study data and records
Compliance & Documentation
Maintain documentation in accordance with FDA and IRB guidelines
Ensure accuracy and completeness of records
Study Closure
Assist in study close-out activities
Required Skills
Basic clinical research knowledge
Data entry and database handling
Strong communication and coordination skills
Organizational and multitasking abilities
Ability to work independently and in a team
Keywords
Clinical Research Jobs, Research Assistant Kanpur, Clinical Trials India, Pharma Jobs India, Entry Level Clinical Research, Hospital Research Jobs, Data Entry Clinical Research
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