On-Site Research Assistant (Part-Time) – Clinical Research
Location: Nagpur, Maharashtra, India
Work Setting: Hospital-Based | On-Site
Employment Type: Part-Time (24 Hours per Week)
Contract Duration: 1 Year (Extension Possible)
Job Requisition ID: JR 9146
About the Organization
ProPharma is a global life sciences consulting organization supporting biotechnology, pharmaceutical, and medical device companies across the complete product lifecycle. Through its advise–build–operate model, the organization delivers expertise in regulatory sciences, clinical research solutions, pharmacovigilance, medical information, quality & compliance, and R&D technology. With over two decades of experience, ProPharma partners with global sponsors to accelerate innovation while ensuring regulatory compliance and patient safety.
About the Role
ThePharmaDaily.com invites applications for the position of On-Site Research Assistant in Nagpur, Maharashtra. This hospital-based, part-time opportunity is ideal for professionals seeking hands-on experience in clinical research site operations, study coordination, and regulatory-compliant documentation.
The Research Assistant will support day-to-day clinical trial activities at the study site, including patient pre-screening, data entry, site communication, and database monitoring. This role offers valuable exposure to FDA and IRB-compliant research practices within a structured clinical trial environment.
Key Responsibilities
Serve as the primary point of contact for daily site communications, document submissions, and study activity coordination
Support patient pre-screening activities as assigned
Perform data entry into clinical databases and respond to system-generated queries
Monitor clinical data systems to ensure accuracy and completeness
Maintain site documentation in compliance with IRB and FDA policies
Assist with study closeout activities and regulatory documentation
Provide support for additional study-related tasks as directed by the study team
Eligibility & Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related healthcare discipline
Alternatively, minimum 3 years of related clinical research or healthcare experience may be considered equivalent
Basic understanding of clinical research processes and regulatory compliance preferred
Proficiency in Microsoft Operating Systems and web-based research platforms
Strong verbal and written communication skills
Professional demeanor and ability to interact effectively with healthcare staff and research teams
Experience Required
0–3 years of experience in clinical research, site coordination, hospital research support, or healthcare operations
Prior study team experience will be an added advantage
Core Competencies
Strong critical thinking and analytical skills
Ability to work independently and collaboratively within a clinical study team
High level of organization and multitasking ability
Professional communication and documentation skills
Ability to maintain patient privacy and confidentiality
Initiative-driven while adhering to study protocols and directives
Work Environment
This is a hospital-based, on-site role in Nagpur, Maharashtra. Candidates must be comfortable working within a clinical environment and adhering to regulatory and institutional guidelines.
Diversity & Equal Opportunity
The organization promotes diversity, equity, and inclusion, fostering a workplace environment where professionals can grow and contribute meaningfully. All applications are reviewed individually by the recruitment team.
Application Process
Applications will be evaluated based on academic qualifications, relevant clinical research exposure, and communication skills. Shortlisted candidates will be contacted for further assessment and interview rounds.
This opportunity is well-suited for candidates seeking practical experience in clinical trial site management, regulatory documentation, and hospital-based research operations within the life sciences industry.
Uttar Pradesh :
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