Life Sciences Job at Parexel | Patient Safety Associate | Apply Now
Parexel, a global leader in clinical research, is currently hiring for the position of Patient Safety Associate I across its major Indian hubs in Hyderabad, Bengaluru, and Mohali. This Life Science Job is a foundational role within the Medical Sciences category, perfect for individuals looking to start a Parexel career in pharmacovigilance (PV). As an Associate I, you will be at the front lines of drug safety, managing Individual Case Safety Reports (ICSRs), performing literature surveillance, and ensuring global regulatory compliance for innovative medical treatments. If you are seeking your next Life Sciences Job, this opportunity is designed for you.
- Job Position: Patient Safety Associate I
- Location: Hyderabad, Bengaluru, Mohali
- Job ID: R0000039196
- Category: Medical Sciences
About the Company
Parexel is one of the world’s largest and most respected Clinical Research Organizations (CROs), providing a full suite of Phase I-IV clinical development services. The company’s core mission is to “bring miracles to life” by accelerating the development of innovative therapies that improve world health. With a “Patient-First” priority, Parexel integrates deep scientific expertise with advanced technology to manage complex global trials while maintaining the highest standards of safety and integrity. Notably, working in a Life Sciences Job such as this at Parexel enables employees to collaborate in a vibrant culture that encourages inquisitiveness, ownership, and continuous professional growth through mentorship and exposure to diverse therapeutic areas.
Key Responsibilities
In this role, you will be responsible for the end-to-end processing of safety data to identify potential risks associated with pharmaceutical products. Furthermore, those passionate about a Life Sciences Job will appreciate the responsibility of ensuring thorough risk management in drug development.
- ICSR Case Processing: Monitor incoming reports from mailboxes, literature, and EudraVigilance. You will perform data entry, triage reports for validity, and ensure medically cohesive narratives are prepared for every case. By pursuing a Life Sciences Job with these responsibilities, you support critical safety activities in clinical research.
- Medical Coding: Utilize the MedDRA (Medical Dictionary for Regulatory Activities) system to accurately code adverse events, suspect products, and medical history in accordance with “Points to Consider” guidelines.
- Safety Submissions: Submit ICSRs and Periodic Reports to Regulatory Authorities and Ethics Committees, maintaining a strong understanding of the global submission landscape and eTMF filing. This task is an important part of a Life Sciences Job—ensuring compliance and quality in pharmacovigilance reporting.
- Literature Monitoring: Formulate and execute search strategies to retrieve scientific articles, screening them for potential adverse drug reactions (ADRs) or emerging safety signals.
- Regulatory Intelligence: Research and maintain safety reporting requirements for assigned countries, ensuring all internal repositories and trackers are updated per SOPs. Candidates attracted to a dynamic Life Sciences Job will find this task both challenging and rewarding.
Qualifications & Skills: Microbiology Job
This position is ideal for graduates with a background in specialized bio-sciences such as a Microbiology Job or Biotechnology. Moreover, those seeking a Life Sciences Job will benefit from experience in these disciplines.
- Education: A degree in Life Sciences, Health, or Biomedical Sciences (e.g., Microbiology, Biochemistry, Biotechnology) is required.
- Experience: While this is an entry-level Associate I role, related experience in a healthcare environment is considered a significant advantage for anyone pursuing a Life Sciences Job.
- Knowledge: You should have a basic understanding of healthcare terminology and a strong desire to learn ICH-GCP guidelines and regional safety requirements.
- Technical Skills: Proficiency in MS Office and an introductory familiarity with pharmacovigilance databases (such as Argus or ArisG) is preferred.
- Soft Skills: Requires excellent communication, foundational problem-solving abilities, and the capacity to work under close supervision while meeting tight regulatory timelines. These soft skills are crucial for excelling in a Life Sciences Job and advancing your career in the medical science field.
In summary, the Patient Safety Associate I role is a definitive Life Science Job for those who want to master the complexities of global drug safety. Launching your Parexel career in this capacity provides exposure to high-level clinical operations, from MedDRA coding to regulatory submissions and literature signal detection. Because this role is available in multiple locations (Hyderabad, Bengaluru, and Mohali), it offers geographic flexibility within one of the top CROs in the world. If you have a degree in the biological sciences and a keen eye for detail, Parexel’s Medical Sciences team is an excellent place to build your expertise.
