Looking for remote clinical research jobs in India? Indero is hiring for the position of TMF Document Coordinator I for its Regulatory Affairs and Clinical Operations team. This home-based CRO job is ideal for candidates with experience in clinical research, Trial Master File (TMF) management, regulatory documentation, and GCP compliance.

Candidates with a life sciences background and experience in pharmaceutical, biotechnology, or CRO industries can apply for this exciting opportunity. The role offers flexible work schedules, career growth, and exposure to global clinical trials.

About Indero CRO

Indero CRO Official Website is a globally recognized clinical research organization specializing in dermatology and rheumatology clinical trials. Formerly known as Innovaderm, the company has over 25 years of experience in global clinical research and trial delivery.

Indero supports pharmaceutical and biotech sponsors with protocol design, patient recruitment, monitoring, biometrics, and regulatory compliance services across North America, Europe, Asia Pacific, and Latin America.

Job Details

Key Responsibilities of TMF Document Coordinator I

The TMF Document Coordinator I will support the maintenance and quality control of the Sponsor’s Trial Master File during clinical trials.

Main Responsibilities

• Review TMF records for completeness, accuracy, and regulatory compliance
• Process TMF documents through quality control workflows
• Classify records and assign appropriate metadata
• Identify document quality issues and coordinate query resolution
• Participate in TMF quality review activities
• Maintain study milestones and expected document lists
• Assist with monthly TMF metrics and reporting
• Attend TMF focus meetings and provide updates
• Collaborate with project teams to resolve TMF-related issues
• Ensure compliance with SOPs, ICH-GCP, FDA, and Health Canada guidelines

Eligibility Criteria

Candidates applying for this remote clinical research job in India should meet the following qualifications:

• College degree in Life Sciences, Pharmacy, Biotechnology, or related field
• Experience in clinical research, CRO, biotechnology, or pharmaceutical industry
• Good understanding of Trial Master File (TMF) processes
• Knowledge of ICH-GCP and FDA regulations
• Strong English communication skills
• Proficiency in Microsoft Word and Excel
• Excellent organizational and multitasking abilities
• High attention to detail and accuracy

Preferred Skills

• TMF document management experience
• Regulatory affairs knowledge
• Clinical trial documentation handling
• Quality control and compliance review skills
• Ability to work in remote and cross-functional teams

Salary Details

Based on current CRO industry standards in India, the expected salary for the TMF Document Coordinator I role at Indero may range between:

₹4.5 LPA – ₹7.5 LPA (Estimated)

Salary may vary depending on experience, TMF expertise, and clinical research background.

Benefits Offered by Indero

Employees joining Indero CRO will receive:

• Flexible work schedule
• Permanent full-time employment
• Remote work opportunity in India
• Ongoing learning and development programs
• International clinical research exposure
• Career growth opportunities in TMF and regulatory operations

Why This TMF Coordinator Job is Important

The demand for TMF specialists, clinical document coordinators, and remote CRO professionals is increasing rapidly in the pharmaceutical and biotechnology industry. Companies conducting global clinical trials require accurate and compliant Trial Master File management to meet regulatory standards.

This Indero TMF Document Coordinator I job provides excellent exposure to:

• Clinical trial documentation
• Regulatory compliance
• CRO operations
• Quality assurance workflows
• Global sponsor communication

How to Apply

Application Link