Hatch Pros is hiring a 3rd Party Clinical Data Specialist for a remote contract opportunity in India, reporting to Cambridge, MA. This remote clinical data specialist role is ideal for professionals experienced in clinical data acquisition, third-party data management, FDA compliance, and Veeva systems.
If you have strong exposure to external clinical data integration, Veeva Vault, TMF documentation, and ICH regulatory standards, this opportunity offers global project exposure in a fast-paced clinical development environment.
Job Overview
- Role: 3rd Party Clinical Data Specialist
- Location: Remote (India)
- Reporting To: Cambridge, MA
- Employment Type: Contract
- Compensation: $8–$10 per hour (approx. ₹660–₹830/hour)
This remote clinical data specialist position focuses on managing external/third-party clinical trial data, ensuring regulatory compliance, and supporting data integration pipelines for drug development programs.
Key Responsibilities
The Clinical Data Specialist will:
- Serve as subject matter expert (SME) for planning and acquisition of third-party clinical data.
- Manage study-level activities including startup, conduct, and closeout.
- Draft and manage external data transfer agreements aligned with regulatory and company standards.
- Support infrastructure setup for external data flow into clinical data pipelines.
- Oversee validation and integration of third-party clinical trial data.
- Collaborate with Clinical Data Management, Clinical Data Engineering, Standards, and Study Execution Teams.
- Ensure proper documentation in the Trial Master File (TMF).
- Support regulatory submission readiness and inspection/audit activities.
- Review work from external vendors including laboratories and eCOA providers.
- Escalate data-related risks to CT3 leadership when necessary.
Technical & Functional Requirements
Essential Skills
- Strong knowledge of FDA and ICH regulations
- Experience across all phases of drug development
- Extensive expertise in clinical data acquisition and management
- Ability to negotiate and manage data transfer agreements
- Understanding of quality control and compliance standards
- Strong cross-functional collaboration skills
Preferred Skills
- Experience with:
- Veeva Vault (access management)
- Veeva CDMS
- Veeva TMF
- Elluminate
- Globalscape (FTP secure transfer tools)
- Leadership experience in data verification teams
Salary & Compensation
- Hourly Rate: $8–$10 per hour
- Approximate INR Equivalent: ₹660 – ₹830 per hour
- Estimated monthly earnings (160 hours): ₹1,05,000 – ₹1,32,000
Compensation may vary based on experience and project scope.
Who Should Apply?
This remote clinical data specialist job in India is suitable for:
- Clinical Data Managers
- Clinical Data Engineers
- CDMS Specialists
- TMF Documentation Experts
- Professionals experienced in third-party clinical trial data integration
- Candidates with Veeva Vault and regulatory compliance experience
Benefits of This Role
- 100% Remote opportunity (India-based)
- Global exposure reporting to US stakeholders
- Hands-on experience in regulatory submission readiness
- High-impact role in external clinical data governance
- Opportunity to work across full drug development lifecycle
How to Apply
