Freelance Study Coordinator ProPharma remote job India 2026. Check eligibility, responsibilities, salary, and apply online for clinical research role today.
Introduction
If you are aiming to grow your career in clinical research while enjoying flexible working hours, this opportunity is worth exploring. The Freelance Study Coordinator at ProPharma offers a part-time remote role where professionals can contribute to global clinical trials. This position is ideal for individuals with prior experience in study coordination, clinical operations, or trial management.
With increasing demand for remote clinical research jobs in India, this role provides both exposure and flexibility. Let’s explore complete details including eligibility, responsibilities, and how to apply.
Job Overview
| Details | Information |
|---|---|
| Job Title | Freelance Study Coordinator |
| Company Name | ProPharma |
| Location | Remote (India) |
| Employment Type | Freelance / Part-time (10 hours per week) |
| Department | Clinical Research / Study Coordination |
| Experience Required | Minimum 1 Year |
| Education | Life Sciences / Nursing / Public Health |
| Salary | As per company standards |
Company Overview
ProPharma is a globally recognized organization providing comprehensive clinical research and regulatory consulting services. The company supports pharmaceutical, biotechnology, and medical device industries across various stages of product development.
With a strong presence in clinical trial management and compliance, ProPharma offers professionals the chance to work on international projects while developing expertise in regulatory standards, data management, and study operations.
Job Location & Employment Type
This is a remote job opportunity, allowing candidates to work from anywhere in India. The role is part-time, requiring approximately 10 hours per week, making it ideal for professionals seeking flexible work arrangements or freelance clinical research roles.
Open Positions / Department Details
- Position: Freelance Study Coordinator
- Department: Clinical Research Operations
- Industry: Life Sciences / CRO
- Work Mode: Remote (India-based candidates preferred)
Key Roles & Responsibilities
As a Freelance Study Coordinator at ProPharma, you will play a crucial role in managing and supporting clinical studies. Your responsibilities include:
- Coordinating daily clinical trial activities across sites and teams
- Maintaining accurate study documentation, trackers, and logs
- Acting as a communication bridge between stakeholders, vendors, and clinical sites
- Assisting in study start-up processes and site readiness activities
- Monitoring patient enrollment, timelines, and study progress
- Ensuring compliance with Good Clinical Practice (GCP) and regulatory standards
- Organizing meetings, preparing agendas, and documenting minutes
- Supporting issue resolution and reconciliation processes
- Contributing to training materials and study-related documentation
Eligibility Criteria
Educational Qualification
- Bachelor’s degree in:
- Life Sciences
- Nursing
- Public Health
- Or related discipline
Experience Required
- Minimum 1 year of experience in:
- Clinical Trial Assistant (CTA)
- Clinical Research Associate (CRA)
- Study Coordinator role
Skills Required
- Strong knowledge of clinical trial processes
- Understanding of GCP guidelines
- Excellent communication and organizational skills
- Ability to manage multiple tasks efficiently
- Proficiency in MS Office and study management tools
- Fluency in English and Gujarati
Salary & Benefits
- Salary: As per company standards
- Flexible working hours (10 hours/week)
- Opportunity to work remotely
- Exposure to global clinical research projects
- Hands-on experience in clinical trial coordination
- Skill enhancement in compliance and documentation
Selection Process
The selection process for this role generally includes:
- Application screening
- Shortlisting based on experience and qualifications
- Virtual interview (technical + HR)
- Final selection and onboarding
How to Apply
Interested candidates can apply through the online application link provided by the company. Ensure your resume highlights your clinical research experience, GCP knowledge, and relevant skills.
Important Dates
- Application Deadline: Not specified (Apply early to avoid missing out)
Why Apply for This Job?
Choosing the Freelance Study Coordinator ProPharma job can be a smart move for your career because:
- It offers flexibility with part-time remote work
- You gain experience with a global CRO company
- Enhances your understanding of clinical trial management
- Provides exposure to international regulatory standards
- Ideal for professionals looking to balance work and personal commitments
FAQs
1. Who can apply for this job?
Candidates with a degree in Life Sciences, Nursing, or Public Health and at least 1 year of clinical research experience can apply.
2. What is the salary for this role?
The salary is not disclosed but will be offered as per company standards.
3. Is this a full-time or part-time job?
This is a part-time freelance role, requiring around 10 hours per week.
4. Is prior experience mandatory?
Yes, at least 1 year of experience in clinical research roles like CTA, CRA, or Study Coordinator is preferred.
5. What skills are required for this role?
Candidates should have knowledge of GCP, clinical trial processes, communication skills, and proficiency in documentation and MS Office.
Conclusion
The Freelance Study Coordinator at ProPharma is an excellent opportunity for clinical research professionals seeking flexibility and global exposure. With remote working benefits and hands-on experience in trial coordination, this role can significantly enhance your career in the clinical research domain. If you meet the eligibility criteria, consider applying as soon as possible.
Disclaimer
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