Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

On-Site Research Assistant (Part Time) - Kanpur, Uttar Pradesh

Propharma
Propharma
0-3 years
Not Disclosed
India
10 April 24, 2026
Job Description
Job Type: Contract Freelance Full Time Hybrid Part Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding

Research Assistant (Clinical Research) – Hospital-Based | Kanpur, Uttar Pradesh | Part-Time | ProPharma Careers

About ProPharma
ProPharma is a leading global consulting organization with over 20 years of experience supporting pharmaceutical, biotechnology, and medical device companies. Through its advise-build-operate model, ProPharma delivers comprehensive solutions across regulatory sciences, clinical research, pharmacovigilance, medical information, and quality & compliance. The company enables clients to accelerate development timelines and successfully bring innovative therapies to market.

Job Overview
ProPharma is hiring a Research Assistant for a hospital-based clinical research role in Kanpur, Uttar Pradesh. This is a part-time, on-site opportunity designed for candidates interested in gaining hands-on experience in clinical trial operations, site coordination, and regulatory documentation.

Job Location & Work Model

  • Location: Kanpur, Uttar Pradesh, India

  • Work Type: On-site (Hospital-based)

  • Employment Type: Part-Time (24 hours per week)

  • Contract Duration: 1 year (extendable based on project requirements and performance)

Key Responsibilities

  • Serve as the primary point of contact for day-to-day site communications and coordination

  • Support pre-screening of study participants as assigned

  • Perform data entry and manage clinical research databases

  • Review and respond to system-generated queries

  • Maintain effective communication with site teams and stakeholders

  • Ensure documentation complies with IRB and FDA regulations

  • Assist with study closeout activities and documentation

  • Support additional study-related tasks as required

Required Skills and Competencies

  • Proficiency in Microsoft Office and web-based clinical research tools

  • Strong analytical and critical thinking abilities

  • Excellent written and verbal communication skills

  • Ability to work independently and collaboratively in a team environment

  • Strong organizational and multitasking skills

  • High attention to detail and commitment to data accuracy

  • Ability to maintain confidentiality and data privacy standards

  • Professional demeanor with strong interpersonal skills

  • Self-motivated with the ability to follow study protocols

Educational Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field

  • Equivalent relevant 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 hospital-based research or clinical trials is an advantage but not mandatory

Why Join ProPharma

  • Gain real-world experience in clinical research within a hospital setting

  • Work on active clinical trials and regulatory processes

  • Collaborative and inclusive work environment

  • Opportunity to build a long-term career in clinical research

Diversity, Equity, and Inclusion
ProPharma is committed to fostering a diverse and inclusive workplace where employees can thrive and contribute meaningfully. The organization values innovation, collaboration, and equal opportunity.

Application Process
All applications are reviewed by ProPharma’s recruitment team to ensure a fair and transparent hiring process. Every applicant receives 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 inquiries via phone or email regarding this position are not permitted.