Life Science Jobs | Parexel is Hiring Patient Safety Specialist | Apply Now
If you are a life science graduate looking to enter the clinical research and pharmaceutical industry without extensive laboratory work, this opportunity under Parexel Career can be a perfect move. A Life Sciences Job at Parexel offers a strong entry into global drug development through pharmacovigilance and patient safety roles. Pharmacovigilance professionals play a critical role in monitoring drug safety, evaluating adverse events, and protecting patient health worldwide.
- Position: Patient Safety Specialist
- Location: India, Hyderabad
- Job ID: R0000038090
- Category: Medical Sciences
About the Company
Parexel is a leading global Clinical Research Organization (CRO) providing advanced drug development, regulatory consulting, and clinical trial solutions to pharmaceutical and biotechnology companies worldwide. The company operates across multiple countries supporting clinical research, pharmacovigilance, and regulatory services. Parexel focuses on accelerating drug development while maintaining patient safety and regulatory compliance. With strong global collaborations, it offers excellent career growth opportunities for life science professionals entering the pharmaceutical industry.
Key Responsibilities
- Maintain knowledge of drug safety profiles, labeling requirements, and global pharmacovigilance regulations
- Implement project workflows and ensure compliance with regulatory reporting timelines and documentation standards
- Support ICSR processing, case assessment, narratives preparation, quality control, and safety report generation
- Execute safety submissions including ICSR, periodic reports, and regulatory authority submissions
- Assist in audit and inspection preparation while maintaining compliant documentation and archiving procedures
- Perform literature search, review scientific publications, and identify adverse drug reactions and safety signals
- Coordinate safety communication between global teams, affiliates, clients, and regulatory authorities
- Support regulatory intelligence activities including monitoring global regulatory updates and maintaining databases
- Assist with regulatory submissions, product lifecycle management, data validation, and reconciliation activities
- Collaborate with cross-functional teams, monitor compliance metrics, identify risks, and support continuous quality improvement initiatives
Education
Degree in Life Science, or other health-related field, or equivalent qualification/work experience
- Experience in safety case management and regulatory reporting
- Basic proficiency with safety databases and data analysis
- Knowledge of ICH guidelines and regional requirements
- Willingness to learn and develop process improvement skills
- Experience in pharmaceutical or healthcare environments preferred
- Knowledge of pharmacovigilance or regulatory regulations and pharmacovigilance processes
- Good analytical and problem-solving abilities
- Effective communication skills
- Strong organizational and time management capabilities
- Familiarity with pharmacovigilance or regulatory systems and databases
This Life Sciences Job through Parexel career openings provides an excellent opportunity for graduates aiming to enter the pharmaceutical industry through pharmacovigilance jobs. With growing demand for drug safety professionals worldwide, this role offers strong career stability, international exposure, and future advancement into regulatory and clinical leadership positions.
