Research Assistant (Clinical Research) – Hospital-Based | Nagpur, Maharashtra | Part-Time | ProPharma Careers
About ProPharma
ProPharma is a globally recognized consulting organization with over 20 years of expertise in supporting pharmaceutical, biotechnology, and medical device companies. Through its advise-build-operate model, ProPharma delivers end-to-end solutions across regulatory sciences, clinical research, pharmacovigilance, medical information, and quality compliance, enabling clients to accelerate innovation and bring safe, effective therapies to patients worldwide.
Job Overview
ProPharma is hiring a Research Assistant for a hospital-based clinical research role in Nagpur, Maharashtra. This is a part-time, on-site position requiring 24 hours per week. The role involves supporting clinical trial operations, site coordination, and data management activities while ensuring compliance with regulatory and ethical standards.
Job Location & Work Model
Location: Nagpur, Maharashtra, India
Work Type: On-site (Hospital-based)
Employment Type: Part-Time (24 hours/week)
Contract Duration: 1 year (extendable based on performance and project needs)
Key Responsibilities
Act as the primary point of contact for daily site communications and coordination
Support pre-screening of study participants as assigned
Perform data entry and manage clinical databases
Evaluate and respond to system-generated queries
Ensure timely and effective communication with site stakeholders
Maintain study documentation in compliance with IRB and FDA guidelines
Assist in study closeout activities and documentation
Support additional study-related tasks as required by the research team
Required Skills and Competencies
Proficiency in Microsoft Office and web-based clinical research platforms
Strong critical thinking and analytical skills
Excellent written and verbal communication abilities
Ability to work independently and collaboratively in a clinical research team
Strong organizational and multitasking capabilities
Professional attitude with attention to detail and data accuracy
Ability to maintain confidentiality and data privacy in a clinical setting
Willingness to take initiative while adhering to study protocols and guidelines
Educational Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field
Equivalent experience may be considered
Experience Requirements
Minimum: 0–3 years of experience in clinical research or related field
Freshers: Eligible to apply
Prior experience in a clinical study team or hospital research setting is preferred but not mandatory
Why Join ProPharma
Opportunity to gain hands-on experience in clinical research at a hospital site
Exposure to real-world clinical trials and regulatory processes
Collaborative and inclusive work environment
Career development opportunities within global clinical research projects
Diversity, Equity, and Inclusion
ProPharma is committed to fostering a diverse and inclusive workplace where all employees are empowered to succeed. The company values innovation, collaboration, and equal opportunity for all individuals.
Application Process
All applications are reviewed by ProPharma’s recruitment team, ensuring a fair and transparent hiring process. Every applicant will receive a response regarding their application status. ProPharma does not use AI-based screening tools.
Important Notice
ProPharma does not accept unsolicited resumes from third-party recruiters. Direct outreach via phone or email regarding this role is not permitted.
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