Indero Hiring TMF Document Coordinator I in India | Remote Clinical Research Jobs 2026

(Indero Hiring TMF Document Coordinator I in India)

Introduction

Remote clinical research jobs in India are growing rapidly as global CROs and pharmaceutical companies continue expanding digital clinical trial operations. Indero CRO has announced an exciting work-from-home opportunity for the position of TMF Document Coordinator I in its Regulatory Affairs and Clinical Operations team.

This remote CRO job is ideal for candidates with backgrounds in:

• Clinical research
• Regulatory affairs
• TMF operations
• Clinical documentation
• Pharmaceutical compliance
• Biotechnology operations

Candidates with experience in Trial Master File (TMF) management, clinical trial documentation, GCP compliance, and regulatory workflows can benefit significantly from this opportunity.

The role provides:

• Permanent full-time remote work
• Flexible work schedules
• Global clinical trial exposure
• CRO operational experience
• Career growth opportunities in TMF and regulatory affairs

As the demand for remote clinical research professionals continues to increase in 2026, TMF specialists and clinical documentation professionals are becoming highly valuable in the pharmaceutical and biotechnology industries.

---

About The Company

Indero CRO is a globally recognized Contract Research Organization (CRO) specializing in dermatology and rheumatology clinical trials.

Previously known as Innovaderm, the company has over 25 years of experience in global clinical research operations and clinical trial management.

Indero supports:

• Pharmaceutical companies
• Biotechnology sponsors
• Clinical research organizations
• Global healthcare partners

through services including:

• Clinical trial management
• Regulatory affairs support
• Patient recruitment
• Biometrics
• Monitoring operations
• TMF management
• Quality compliance

Company Details

• Company Name: Indero CRO
• Former Name: Innovaderm
• Industry: Clinical Research / CRO
• Headquarters: Montreal, Canada
• Founded: 2000
• Global Presence: North America, Europe, Asia Pacific & Latin America
• Employee Strength: 1,000+ Employees
• Specialization: Dermatology & Rheumatology Clinical Trials

Indero is known for its global clinical operations expertise and remote clinical trial support systems.

---

Job Overview Summary

Indero is hiring a TMF Document Coordinator I for its Regulatory Affairs and Clinical Operations department in India.

This is a:

• Home-based remote job
• Full-time permanent opportunity
• Clinical research documentation role

The selected candidate will support:

• Trial Master File maintenance
• Clinical documentation quality control
• Regulatory compliance workflows
• TMF reporting activities
• Sponsor documentation systems

This role is ideal for candidates looking to build careers in:

• Clinical research operations
• Regulatory affairs
• TMF management
• Clinical documentation
• CRO quality systems

Candidates will gain exposure to:

• Global clinical trial workflows
• FDA and ICH-GCP compliance
• TMF quality review activities
• International sponsor communication
• Clinical trial documentation systems

---

Vacancy Details

Job Details	Information
Job Role	TMF Document Coordinator I
Company	Indero CRO
Industry	Clinical Research / CRO
Work Mode	Home-Based / Remote
Job Type	Permanent, Full-Time
Department	Regulatory Affairs / TMF Operations
Location	India
Experience	Clinical Research Experience Preferred
Qualification	College Degree

---

Responsibility Explanation

1. Trial Master File (TMF) Management

The selected candidate will help maintain the Sponsor’s Trial Master File throughout clinical trial operations.

Responsibilities Include:

• Reviewing TMF records
• Organizing clinical trial documents
• Managing document tracking systems
• Supporting TMF completeness reviews

TMF management is critical for regulatory inspections and clinical trial compliance.

---

2. Regulatory Documentation Quality Control

The role involves quality review and compliance verification of clinical research documentation.

Responsibilities Include:

• Checking document accuracy
• Identifying missing information
• Supporting query resolution
• Maintaining regulatory standards

Strong attention to detail is highly important for this responsibility.

---

3. Metadata & Document Classification

Candidates will classify TMF documents and assign appropriate metadata in documentation systems.

Activities Include:

• Organizing clinical records
• Managing document indexing
• Supporting electronic documentation systems
• Maintaining accurate filing structures

This ensures smooth retrieval of regulatory documents during audits and inspections.

---

4. TMF Reporting & Study Milestones

The role also includes tracking TMF metrics and maintaining study timelines.

Responsibilities:

• Assisting monthly TMF reporting
• Tracking expected document lists
• Supporting milestone management
• Participating in TMF review meetings

Candidates with strong organizational skills may perform well in this area.

---

5. Regulatory Compliance Support

The selected candidate will ensure compliance with:

• SOPs
• ICH-GCP guidelines
• FDA regulations
• Health Canada requirements

This role supports global clinical trial quality standards and regulatory readiness.

---

Eligibility Criteria

Educational Qualification

Candidates with the following qualifications can apply:

• Life Sciences
• Pharmacy
• Biotechnology
• Related Healthcare Fields
• College Degree Holders

---

Experience Required

Candidates with experience in:

• Clinical research
• CRO operations
• Pharmaceutical industry
• Biotechnology industry
• Clinical documentation

will have an advantage.

---

Skills Required

Technical Skills

Important technical skills include:

• TMF document management
• Clinical trial documentation handling
• Regulatory affairs understanding
• Microsoft Word and Excel proficiency
• Quality control review skills
• Clinical compliance knowledge

---

Soft Skills

Candidates should possess:

• Strong English communication
• Organizational abilities
• Attention to detail
• Multitasking skills
• Team collaboration capability
• Problem-solving skills

Remote work discipline and time management are also important.

---

Preferred Skills

Candidates with the following additional skills may have stronger selection chances:

• TMF operations experience
• Regulatory documentation exposure
• CRO workflow understanding
• FDA and ICH-GCP knowledge
• Cross-functional team coordination
• Remote work experience

---

Salary Estimate

Based on current CRO and clinical research market trends in India, the estimated salary for this role may range between:

Estimated Salary:

• ₹4.5 LPA – ₹7.5 LPA

Salary may vary depending on:

• TMF expertise
• Clinical documentation experience
• CRO background
• Regulatory knowledge
• Communication skills

---

Benefits Offered by Indero

Employees joining Indero CRO may receive:

• Permanent remote work opportunity
• Flexible work schedules
• Global clinical trial exposure
• Learning and development programs
• International regulatory operations experience
• Career growth in TMF and regulatory affairs

This role offers excellent exposure to global clinical research systems.

---

Why This TMF Coordinator Role is Important

The pharmaceutical and biotechnology industries are rapidly increasing demand for:

• TMF specialists
• Clinical document coordinators
• Regulatory operations professionals
• Remote clinical research staff

Accurate Trial Master File management is essential for:

• Regulatory inspections
• Clinical trial audits
• Sponsor compliance
• Global regulatory approvals

This role provides hands-on experience in:

• Clinical documentation systems
• Regulatory workflows
• CRO quality operations
• Clinical trial compliance

---

Interview Details

Selection Process

The recruitment process may include:

1. Resume Shortlisting
2. HR Screening
3. TMF Operations Discussion
4. Regulatory Compliance Interview
5. Final Selection Round

---

Topics Candidates Should Prepare

Candidates should revise:

• TMF basics
• ICH-GCP guidelines
• Clinical trial phases
• Regulatory documentation
• FDA compliance basics
• Clinical research terminology
• CRO operational workflows

Strong communication and documentation understanding can improve selection chances.

---

Required Documents

Candidates should prepare the following documents:

• Updated Resume/CV
• Educational Certificates
• Experience Certificates
• Government ID Proof
• Passport-size Photograph
• Current Salary Details (if applicable)
• Clinical Research Training Certificates
• Internship Documents

Keeping documents organized can help during the interview and onboarding processes.

---

How to Apply

Interested candidates can apply through the official application link below:

Apply for TMF Document Coordinator I

Candidates are advised to prepare professional resumes highlighting:

• TMF operations exposure
• Clinical research experience
• Regulatory documentation skills
• GCP knowledge
• CRO experience

---

Frequently Asked Questions (FAQs)

1. Which company is hiring for this remote clinical research job?

Indero CRO is hiring for the TMF Document Coordinator I role.

---

2. Is this a work-from-home job?

Yes, this is a home-based remote clinical research job in India.

---

3. Which qualifications are eligible?

Candidates with Life Sciences, Pharmacy, Biotechnology, and related healthcare degrees can apply.

---

4. What experience is preferred?

Clinical research, CRO, biotechnology, or pharmaceutical industry experience is preferred.

---

5. What is TMF in clinical research?

TMF stands for Trial Master File, which contains essential clinical trial documents required for regulatory compliance and inspections.

---

6. What is the expected salary range?

The estimated salary range is approximately ₹4.5 LPA – ₹7.5 LPA.

---

7. Which skills are important for this role?

TMF management, regulatory documentation, ICH-GCP knowledge, communication skills, and organizational ability are important.

---

8. Does this role provide global clinical trial exposure?

Yes, the role provides exposure to international clinical trial operations and regulatory systems.

---

Final Conclusion

Indero’s TMF Document Coordinator I role provides an excellent opportunity for pharmacy, life sciences, and biotechnology professionals looking to build careers in remote clinical research and regulatory operations.

The position offers:

• Work-from-home flexibility
• Exposure to global clinical trials
• Regulatory documentation experience
• CRO operational learning
• Career growth in TMF management

As global pharmaceutical companies continue expanding remote clinical trial operations in 2026, professionals with expertise in:

• TMF management
• Regulatory affairs
• Clinical documentation
• CRO operations
• GCP compliance

will remain highly valuable in the healthcare industry.

Candidates interested in clinical research operations and remote CRO careers should consider applying for this opportunity.

---

Disclaimer

Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.

---

🚨 Not Getting Interview Calls in Pharma?

Even after applying to multiple companies, still no response.

👉 The real problem is NOT your qualification —
it’s your resume + wrong job strategy

Most pharma candidates: ❌ Use non-ATS resumes
❌ Apply randomly without direction
❌ Don’t match recruiter expectations

That’s why they don’t get shortlisted.

---

✅ Here’s How Pharma Duniya Can Help You

We don’t just “make resumes” —
We help you get results 👇

✔ ATS-Friendly Resume (PV / QA / QC / Clinical – role-based)
✔ Proper Job Direction (which domain is best for you)
✔ Daily Apply Strategy (where & how to apply)
✔ Interview Preparation (real pharma questions)
✔ Personal Guidance (step-by-step support)

---

🎯 Choose What You Need

👉 Resume Only (ATS Optimised)
👉 Resume + Basic Guidance
👉 Complete Career Guidance
👉 Premium Mentorship (for serious candidates)

---

🚀 Start Now

👉 Click here to check full details & get started:

🔗 [Pharma Career Support & Resume Service]

📲 WhatsApp support available after form submission

Share on WhatsApp

Recommended Pharma Career & Job Updates (Must Read)

If you are preparing for pharma job interviews or actively searching for the latest QA, QC, Pharmacovigilance jobs and walk-in interviews, don’t miss these important and student-friendly career resources from Pharma Duniya 👇

"Sun Pharma Walk-In Interview 2026 for QC, QA & Microbiology Departments | Pharma Jobs in Gujarat"💜🔥

"Arcolab Hiring XEVMPD/PSMF Associate in Bengaluru | Pharmacovigilance Jobs India 2026"❤️🔥

"MS Clinical Research Hiring Data Monitoring & eCRF Designer in Bengaluru | Clinical Data Management Jobs 2026"💥💖

📢 Stay Updated with Latest Pharma Jobs & Walk-In Interviews

If you want daily verified updates on QA, QC, Pharmacovigilance, Clinical Research, and Pharma Walk-In Interviews, join Pharma Duniya’s official channels and never miss an opportunity.

✅ Join our WhatsApp Group
✅ Join our Telegram Channel

📌 Get verified pharma job alerts, interview tips, resume guidance, and student career support directly on your phone.

🌐 Visit us daily for the latest updates:
👉 www.pharmaduniya.com