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Hiring TMF Document Coordinator I
Indero CRO is hiring TMF Document Coordinator I for its Regulatory Affairs and Clinical Operations team in India.
This remote CRO opportunity is ideal for candidates with experience in Clinical Research, Trial Master File (TMF) Management, Regulatory Documentation, GCP Compliance, and Clinical Operations.
📘 Learn More: Clinical Research Coordinator Career Guide
📋 Indero CRO Recruitment 2026 – Overview
- Company: Indero CRO
- Role: TMF Document Coordinator I
- Industry: Clinical Research / CRO
- Employment Type: Permanent Full-Time
- Work Mode: Remote / Home-Based
- Location: India
- Department: Regulatory Affairs / TMF Operations
- Experience: 1 Year+
🏢 About Indero CRO
Indero CRO is a globally recognized clinical research organization specializing in dermatology and rheumatology clinical trials. Formerly known as Innovaderm, the company supports global pharmaceutical and biotechnology sponsors with clinical trial delivery, monitoring, biometrics, and regulatory compliance services.
📌 Key Responsibilities
- Review TMF records for completeness and compliance
- Process TMF documents through quality workflows
- Classify documents and assign metadata
- Identify quality issues and coordinate query resolution
- Participate in TMF quality review activities
- Maintain study milestones and expected document lists
- Support monthly TMF metrics and reporting
- Collaborate with cross-functional project teams
- Ensure compliance with SOPs, ICH-GCP, FDA, and Health Canada guidelines
📚 Learn TMF & Clinical Documentation: Clinical Documentation & CDISC Guide
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- BSc / MSc
- Life Sciences
- Biotechnology
- Clinical Research Background
- 1+ Years Experience Preferred
💻 Required Skills
- TMF document management
- Regulatory affairs understanding
- ICH-GCP & FDA guideline knowledge
- Clinical trial documentation handling
- Microsoft Word & Excel proficiency
- Quality control and compliance review
- Attention to detail & multitasking
- Strong English communication skills
🧠 Practice Here: Drug Safety & Clinical Research Quiz
🎁 Benefits of Working at Indero
- Flexible work schedule
- Permanent remote work opportunity
- International clinical trial exposure
- Career growth in TMF & regulatory operations
- Learning and development programs
- Global sponsor communication exposure
📈 Why This TMF Job is Important
The demand for TMF specialists, clinical document coordinators, and remote CRO professionals is increasing rapidly across the pharmaceutical and biotechnology industry.
This role provides exposure to:
- Clinical trial documentation
- Regulatory compliance workflows
- CRO operations
- Quality assurance activities
- Global sponsor communication
- TMF lifecycle management
❓ Frequently Asked Questions
- Is this a remote job? Yes, this is a home-based remote role.
- Who can apply? Candidates from Life Sciences, Pharmacy, Biotechnology, and Clinical Research backgrounds.
- What experience is required? Clinical research experience is preferred.
- What skills are important? TMF management, GCP compliance, documentation handling, and communication skills.
- Is CRO experience mandatory? Preferred but not mandatory.
🧠 Prepare Before Applying
🚀 Job Application Link
Please make sure to read the complete job description carefully before submitting your application. Make sure your qualifications and experience align with the role requirements before proceeding.
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