Parexel Hiring for Remote Clinical Tech Validation
Parexel, a global clinical research organization (CRO), is currently hiring for the position of System Validation Services (SVS) – Specialist II. This remote-based opportunity is based out of Mohali, India, and is designed for candidates with a background in clinical research, life sciences, pharmacy, or information technology. Parexel Hiring for Remote Clinical Tech Validation
This is an ideal position for professionals interested in clinical system validation and technology compliance, particularly within the GxP-regulated environment.
About Parexel
Parexel is one of the world’s leading CROs, delivering clinical trial services, regulatory consulting, and market access solutions to the pharmaceutical, biotechnology, and medical device industries. With operations in more than 100 countries, Parexel is committed to improving global health by helping develop life-changing medicines. Parexel Hiring for Remote Clinical Tech Validation
The company fosters a people-first culture focused on empathy, collaboration, and patient-centered development. Working at Parexel means being part of a mission-driven organization that values expertise and innovation.
Position Details
Role: System Validation Services – Specialist II
Department: Technology Quality Compliance
Location: Remote (Based in Mohali, India)
Experience Required: Minimum 3 years in system validation or clinical research
Work Type: Full-Time (Remote)
Application Mode: Online
Industry: Clinical Research / Pharma IT Compliance
Job Responsibilities
As an SVS Specialist II, you will contribute to ensuring that Parexel’s internal systems meet regulatory compliance standards. The key responsibilities include: Parexel Hiring for Remote Clinical Tech Validation
1. Validation and Compliance
- Lead and execute system validation activities following a risk-based validation approach
- Ensure systems meet regulatory standards, particularly GxP and GCP
- Perform Periodic Reviews to assess and maintain system validation status
- Guide project teams and support validation planning and execution
2. Risk Management
- Support risk assessments related to clinical systems and technologies
- Contribute to audit readiness and participate in regulatory inspections
- Document system issues and support remediation efforts
3. Process and Quality Improvement
- Assist in the development and maintenance of controlled documents related to validation
- Help develop training materials on validation and compliance practices
- Contribute to ongoing process improvement initiatives in system lifecycle management
4. Administrative and Technical Support
- Maintain proper documentation for audits and internal quality checks
- Track validation deliverables, timelines, and ensure compliance documentation is complete and accurate
- Submit regular timesheets and activity logs as per company protocol
Required Qualifications
Educational Background
Candidates must hold one of the following qualifications: Parexel Hiring for Remote Clinical Tech Validation
- B.Pharm / M.Pharm
- B.Tech / M.Tech in Computer Science, IT, or Biotechnology
- B.Sc / M.Sc in Life Sciences or Clinical Research
- Pharm.D
- Diploma in IT Compliance, Quality Assurance, or Clinical Research
Experience
- Minimum 3 years of experience in clinical trials, system validation, or regulatory compliance
- Knowledge of GxP, GCP, 21 CFR Part 11, and other global regulatory standards
- Exposure to System Life Cycle (SLC), Computerized System Validation (CSV), and software development processes
Preferred Skills
- Familiarity with tools such as JIRA, Confluence, or Veeva Vault
- Understanding of Lean Six Sigma and project management methodologies
- Effective communication and problem-solving abilities
- Strong attention to detail and organizational skills
- Ability to manage multiple priorities in a fast-paced, remote environment
Why Join Parexel?
Joining Parexel means becoming part of a mission-driven organization that supports patient-focused innovation and integrity in clinical development. Benefits of working at Parexel include: Parexel Hiring for Remote Clinical Tech Validation
- Remote working flexibility
- Exposure to global clinical development systems
- A collaborative work culture with emphasis on training and upskilling
- Opportunities for career advancement in IT compliance and regulatory operations
- Supportive management and a structured work environment that values quality and precision
How to Apply
Interested candidates are encouraged to apply directly through the Parexel Careers Portal or through verified job platforms. Prepare a professional resume that highlights your experience in clinical system validation, regulatory compliance, and IT documentation. Parexel Hiring for Remote Clinical Tech Validation
Apply before the closing date to ensure consideration. While no specific last date is mentioned, Parexel typically fills such roles quickly, so early application is recommended.
Final Thoughts
This System Validation Services – Specialist II role at Parexel is a valuable opportunity for clinical or IT professionals looking to specialize in technology quality compliance. Whether you come from a life sciences or tech background, this role allows you to contribute to the global healthcare ecosystem by supporting systems that enable clinical research and patient safety. Parexel Hiring for Remote Clinical Tech Validation
If you have a strong eye for detail, knowledge of clinical regulations, and the discipline to work remotely with cross-functional teams, this role is designed for you.
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