Site Visit Report Reviewer (SVRR)

🚀 Parexel Hiring | Site Visit Report Reviewer (SVRR) | Remote Clinical Research Jobs

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🏢 Company: Parexel
💼 Position: Site Visit Report Reviewer (SVRR)
📍 Location: Bengaluru, Karnataka, India (Remote)
🏢 Work Mode: Remote
📄 Employment Type: Full-Time
🏭 Industry: Clinical Research | Pharmaceuticals | Biotechnology

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🏢 About Parexel

Parexel is a global Contract Research Organization (CRO) supporting pharmaceutical and biotechnology companies in clinical development, regulatory solutions, consulting, and healthcare innovation.

The organization works on global clinical research programs focused on improving patient health outcomes and accelerating the development of new therapies.

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📋 Job Description

Parexel is hiring Site Visit Report Reviewer (SVRR) professionals in India.

This opportunity is suitable for candidates with experience in clinical operations, site management, monitoring activities, and clinical research within pharmaceutical, biotech, or CRO environments.

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📌 Job Details

Position: Site Visit Report Reviewer (SVRR)
Company: Parexel
Location: Bengaluru (Remote)
Employment Type: Full-Time
Industry: Clinical Research / Life Sciences

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🎓 Educational Qualification

Candidates with qualifications in:

✔ B.Pharm

✔ M.Pharm

✔ Pharm.D

✔ B.Sc / M.Sc Life Sciences

✔ Nursing

✔ Other Health-Related Disciplines

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📌 Key Responsibilities

🔹 Review Site Qualification Visit Reports.

🔹 Review Site Initiation, Monitoring, and Site Termination Visit Reports.

🔹 Ensure compliance with regulatory requirements, ICH-GCP guidelines, and company procedures.

🔹 Monitor and track:

✔ Open Issues
✔ Protocol Deviations (PDs)
✔ Serious Adverse Events (SAEs)

🔹 Collaborate with Clinical Research Associates (CRAs), Clinical Operations Leaders, and project teams.

🔹 Participate in project meetings and discussions.

🔹 Analyze monitoring visits and identify issue trends.

🔹 Support clinical operations activities after required training.

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🛠 Required Skills

✔ Strong written and verbal communication skills

✔ Good analytical and decision-making ability

✔ Strong attention to detail

✔ Excellent teamwork and interpersonal skills

✔ Ability to manage multiple assignments

✔ Client-focused approach

✔ Problem-solving skills

✔ Time management skills

✔ Microsoft Office proficiency

✔ Ability to work with global teams

✔ Knowledge of ICH-GCP guidelines and clinical research regulations

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⭐ Preferred Experience

Candidates with experience in:

✔ Site Management

✔ Clinical Research Associate (CRA) Role

✔ Clinical Monitoring

✔ Clinical Trial Processes

✔ Pharmaceutical / Biotechnology / CRO Industry

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🌟 Why Join Parexel?

✨ Remote work opportunity

✨ Exposure to global clinical trials

✨ Opportunity to work with international teams

✨ Career growth in clinical research

✨ Learning and professional development opportunities

✨ Meaningful contribution to healthcare innovation

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📧 How to Apply

Interested candidates can apply through the official Parexel career portal.

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