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) - Belagavi, Karnataka

Propharma
Propharma
0-3 years
Not Disclosed
Karnataka, India
10 April 24, 2026
Job Description
Job Type: Contract 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 | Belagavi, Karnataka | Part-Time | ProPharma Careers

About ProPharma
ProPharma is a globally established consulting organization with more than 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—helping clients accelerate innovation and successfully bring therapies to market.

Job Overview
ProPharma is seeking a Research Assistant for a hospital-based clinical research role in Belagavi, Karnataka. This part-time, on-site position involves supporting clinical trial operations, site coordination, and regulatory documentation while ensuring adherence to global compliance standards.

Job Location & Work Model

  • Location: Belagavi, Karnataka, India

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

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

  • Contract Duration: 1 year (with potential extension)

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

  • Review and respond to system-generated queries

  • Maintain effective and timely communication with site teams

  • Ensure all documentation complies with IRB and FDA regulations

  • Assist in study closeout activities and documentation

  • Support additional study-related and administrative tasks as required

Required Skills and Competencies

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

  • Strong analytical and critical thinking skills

  • Excellent written and verbal communication abilities

  • Ability to work independently and collaboratively within a research team

  • Strong organizational and multitasking capabilities

  • High attention to detail and data accuracy

  • Ability to maintain confidentiality and ensure data privacy

  • Professional attitude with strong interpersonal skills

  • Ability to take initiative while following established 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 domain

  • Freshers: Eligible to apply

  • Prior experience in a clinical trial or hospital research setting is preferred but not mandatory

Why Join ProPharma

  • Gain practical experience in hospital-based clinical research

  • Work on real-world clinical trials and regulatory processes

  • Collaborative and inclusive work environment

  • Opportunity to build a career in global clinical research

Diversity, Equity, and Inclusion
ProPharma is committed to creating an inclusive workplace that values diversity and empowers employees to contribute their best. The organization fosters innovation, collaboration, and equal opportunity for all.

Application Process
All applications are reviewed by ProPharma’s recruitment team to ensure a fair and transparent hiring process. Candidates will receive communication 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 role are not permitted.