Remote Safety Physician Job at Parexel, India
Interested in building a career in Pharmacovigilance and Drug Safety with a global clinical research organization? Parexel is hiring a Patient Safety Physician for a remote role in India. This Remote Safety Physician Job at Parexel Careers in India is ideal for MBBS or MD professionals looking to work in medical safety review, adverse event assessment, pharmacovigilance, and regulatory compliance. The role offers exposure to global drug safety operations, clinical trial safety monitoring, and signal detection activities. If you are passionate about patient safety, medical review, and global healthcare regulations, this could be an excellent career opportunity.
About the Company:
Parexel is a leading global clinical research organization (CRO) that supports the development of innovative therapies and healthcare solutions worldwide. The company specializes in clinical trials, regulatory consulting, pharmacovigilance, and medical communications. Parexel works closely with pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate drug development. With a strong focus on innovation, collaboration, and scientific excellence, Parexel offers professionals opportunities to contribute to global healthcare advancements.
Job Details:
- Job Role: Patient Safety Physician
- Job ID: R0000040536
- Category: Medical Sciences
- Location: India
- Work Type: Remote
- Employment Type: Full-Time
- Experience Required: Fresher / Relevant Experience Accepted
Key Responsibilities:
- Perform medical review of adverse event and safety cases including spontaneous, clinical trial, and literature cases.
- Assess seriousness, causality, listedness, and expectedness of adverse events.
- Write Pharmacovigilance and Marketing Authorization Holder (MAH) comments.
- Review narratives for medical coherence and scientific accuracy.
- Provide medical guidance to safety and case processing teams in this Remote Safety Physician Job
- Conduct literature reviews for product safety assessment and signal management activities.
- Support signal detection, validation, and safety alert assessment activities.
- Review and contribute to regulatory safety documents including PSURs, PBRERs, DSURs, and SERs at Parexel Careers
- Participate in safety management meetings and scientific discussions.
- Review adverse event coding, medical histories, and concomitant medications for consistency.
- Support preparation of clinical protocols, journal articles, and safety reports.
- Provide medical expertise for pharmacovigilance workflows and clinical safety monitoring in this Remote Job in India
- Interact with internal teams, healthcare professionals, and other stakeholders to resolve issues.
- Ensure compliance with global pharmacovigilance regulations and reporting timelines.
Educational Requirements for this Job:
- MBBS / MD or medically qualified degree from a recognized medical school.
- Completion of internship, residency, or basic clinical medicine training required.
- Freshers and candidates with relevant pharmacovigilance, clinical practice, or drug safety experience can apply.
Skills Required:
- Strong understanding of medical terminology and clinical medicine
- Knowledge of pharmacovigilance and drug safety principles
- Familiarity with ICH-GCP, GVP, and global drug safety regulations
- Excellent scientific writing and medical review skills
- Strong verbal and written communication abilities
- Attention to detail and analytical thinking
- Ability to work with web-based applications and Microsoft Office tools
- Good presentation and collaboration skills
- Ability to manage multiple tasks within timelines
- Flexibility and willingness to learn new processes and technologies
Benefits of the Remote Safety Physician Job:
- Opportunity to work remotely with a global CRO
- Exposure to international pharmacovigilance and drug safety projects
- Career growth in Medical Safety and Pharmacovigilance
- Hands-on experience with global regulatory safety reporting
- Opportunity to work on clinical trials and post-marketing safety activities
- Collaborative and scientifically driven work environment
- Learning opportunities in signal detection and risk management
- Exposure to global pharmaceutical and biotechnology projects
- Opportunity to develop expertise in medical review and regulatory compliance
- Work with multidisciplinary global healthcare teams
