Paraxel Careers: Apply Now for Patient Safety Associate Position

Paraxel Careers: Apply Now for Patient Safety Associate Position

Paraxel Careers: Parexel is hiring a Patient Safety Associate I for its Hyderabad location. This role is ideal for fresh graduates and early-career professionals in dentistry who want to build a strong foundation in pharmacovigilance, drug safety, and medical monitoring within a global CRO environment. This is a full-time, office-based role with excellent learning exposure, global processes, and structured growth opportunities.

Paraxel Careers—Details:

• Position: Patient Safety Associate I
• Job ID: R0000035109
• Location: India – Hyderabad

About the Company:

Parexel is one of the world’s leading Clinical Research Organizations (CROs), with more than 16,000 employees across 100+ countries. Headquartered near Boston and Durham, Parexel delivers end-to-end clinical development solutions—from clinical trials and regulatory affairs to market access and commercialization.

Paraxel Careers-Qualification:

• Bachelor’s in Dentistry (BDS).
• Related experience in healthcare, pharmacovigilance, or clinical safety is an added advantage.
• Strong communication, documentation, and analytical skills.
• Ability to perform literature and database searches.
• Proficient with computer applications and safety database systems.
• Excellent organizational and time management abilities.
• Ability to work collaboratively in a fast-paced, global team environment.

Role:

The Patient Safety Associate I supports clinical drug safety, pharmacovigilance operations, and medical monitoring activities. The role involves managing Individual Case Safety Reports (ICSRs), performing safety data processing, literature review, regulatory reporting, and ensuring compliance with global pharmacovigilance guidelines and SOPs.

Key Responsibilities:

• Process and triage Individual Case Safety Reports (ICSRs) from multiple sources.
• Perform data entry, coding (using MedDRA), quality checks, and case narrative writing.
• Support project-specific safety database setup and development of data entry guidelines.
• Manage follow-ups, query resolution, and documentation of case files.
• Assist in regulatory submissions, including SUSARs, PSRs, and expedited reporting.
• Conduct literature searches and track regulatory requirements.
• Participate in audits, inspections, team meetings, and client interactions as needed.
• Support Medical Directors/Safety Physicians with safety-related insights.
• Ensure compliance with global safety regulations and Parexel SOPs.
• Maintain project files, working documents, and safety reporting logs.

Why Join Parexel?

Joining Parexel means becoming part of a globally trusted CRO where your work directly impacts patient safety and global healthcare outcomes. You gain hands-on training in world-class pharmacovigilance systems, mentorship from experienced safety leaders, and exposure to international drug development processes. Parexel offers structured career paths, continuous learning programs, and a highly supportive culture rooted in empathy, scientific excellence, and patient-first values. This role provides the perfect launchpad for long-term growth in PV, clinical research, and drug safety operations—making it an ideal opportunity for anyone passionate about advancing medical innovation.

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