Tata Consultancy Services (TCS) Careers is hiring experienced professionals for the role of Clinical Trial Disclosure & Redaction Specialist in India. This opportunity is ideal for candidates with experience in Regulatory Affairs, Clinical Research, Clinical Trial Disclosure, EMA 0070, EUCTR, and document redaction activities.
Professionals with hands-on expertise in clinical document anonymization, confidential information redaction, and global compliance regulations can explore this exciting opportunity to work in a fast-paced regulatory environment.
The role offers exposure to international clinical trial disclosure standards and collaboration with cross-functional global teams.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Trial Disclosure & Redaction Specialist |
| Company | Tata Consultancy Services |
| Experience Required | 2–3 Years |
| Department | Regulatory Affairs / Clinical Research |
| Industry | Clinical Research, Regulatory Affairs |
| Location | India |
| Employment Type | Full-Time |
| Application Mode | Email Application |
Key Responsibilities
Candidates applying for the Clinical Trial Disclosure & Redaction Specialist job at TCS will be responsible for:
- Understanding Clinical Trial Disclosure regulations including EUCTR, EMA 0070, and EMA 0043
- Identifying personal confidential information (PCI) and company confidential data in clinical documents
- Performing redaction and anonymization activities for clinical study documents
- Uploading documents into disclosure management systems
- Coordinating review and approval workflows
- Supporting project planning activities including:
- Project trackers
- Performance matrices
- Meeting coordination
- Documentation support
- Ensuring compliance with global clinical disclosure standards
Required Skills & Qualifications
Educational Qualification
Candidates from the following backgrounds may apply:
- B.Pharm
- M.Pharm
- Life Sciences
- Clinical Research
- Regulatory Affairs
- Related healthcare disciplines
Experience Required
- Minimum 2–3 years of experience in:
- Clinical Research
- Regulatory Affairs
- Clinical Trial Disclosure
- Redaction Activities
Preferred Skills
- Strong understanding of:
- EUCTR
- EMA Policy 0070
- EMA Policy 0043
- Experience with:
- Clinical document anonymization
- Confidentiality review
- Regulatory submissions
- Good communication and stakeholder coordination skills
- Ability to manage timelines and compliance-driven projects
Why Join TCS?
Working with Tata Consultancy Services offers professionals an opportunity to:
- Gain exposure to global clinical compliance frameworks
- Work with international regulatory standards
- Build expertise in clinical trial disclosure and redaction
- Collaborate with global clinical and regulatory teams
- Enhance career growth in Regulatory Affairs and Clinical Operations
How to Apply
Interested candidates can share their updated CV directly via email:
Email ID: manohar.jadhav@tcs.com
Candidates should mention:
- Current Experience
- Notice Period
- Current Location
- Relevant Clinical Trial Disclosure / Redaction Experience
