Hybrid Pharmacovigilance Job at Sanodz, Telangana
Looking for a senior-level pharmacovigilance and drug safety career in the pharmaceutical industry? Sandoz is hiring a Medical Safety Lead for its Research & Development division in Telangana, India. This Hybrid Pharmacovigilance Job at Sanodz Careers is ideal for experienced professionals in drug safety, medical review, and pharmacovigilance operations. The selected candidate for this Job in Telangana will work on clinical safety monitoring, signal detection, adverse event evaluation, and regulatory safety support. The role also involves collaboration with cross-functional medical, regulatory, and clinical development teams. Candidates with strong experience in medical review and pharmacovigilance are preferred.
About the Company:
Sandoz is a global leader in generic and biosimilar medicines, providing affordable and high-quality healthcare solutions across more than 100 countries.
The company has delivered over 900 million patient treatments globally and continues to expand through innovation, partnerships, and advanced pharmaceutical development capabilities. Sandoz focuses on improving access to sustainable and cost-effective medicines worldwide.
Job Details:
- Job Role: Medical Safety Lead
- Job ID: REQ-10028869
- Department: Research & Development
- Business Unit: Administration & Facility
- Job Location: Telangana, India
- Employment Type: Full Time
- Job Type: Regular
- Work Mode: Hybrid/Flexible Work Environment
- Shift Work: No
- Industry: Pharmaceutical / Pharmacovigilance
Key Responsibilities:
- Monitor clinical safety of products and projects
- Conduct literature reviews and safety evaluations in this Hybrid Pharmacovigilance Job
- Review individual adverse event cases and perform signal detection
- Respond to safety-related medical queries
- Perform medical assessment of safety cases
- Collect additional follow-up information when required
- Evaluate product quality defects associated with adverse events
- Review line listings of single safety cases in this Job in Telangana
- Prepare investigator notifications and periodic medical assessments
- Identify and evaluate safety signals from solicited and unsolicited reports as a Medical Safety Lead
- Conduct safety signal monitoring and analysis
- Support responses to regulatory authority and healthcare professional inquiries
- Prepare safety data for health authority review boards
- Provide inputs for legal and country organization safety-related queries at Sandoz Careers
- Evaluate clinical context and medical implications of adverse event reports
- Collaborate with Clinical Development, Regulatory Affairs, Medical Affairs, Epidemiology, and Statistics teams
- Support departmental goals and safety objectives
- Participate in pharmacovigilance and safety management activities
Educational Requirements for this Hybrid Pharmacovigilance Job:
- A medical or scientific-related degree is mandatory
- Healthcare, or medical background preferred
Skills Required:
- Pharmacovigilance expertise
- Drug safety medical review skills
- Signal detection and safety monitoring knowledge
- Adverse event assessment expertise
- Clinical safety evaluation abilities
- Medical data interpretation skills
- Knowledge of regulatory safety requirements
- Literature review and analysis skills
- Scientific communication abilities
- Cross-functional collaboration skills
- Clinical judgment and decision-making abilities
- Regulatory documentation understanding
- Attention to detail and analytical thinking
- Problem-solving and risk assessment skills
- Stakeholder communication abilities
Experience Required:
- Minimum 8+ years of experience in medical review
- Strong experience in Drug Safety or Pharmacovigilance mandatory
- Experience in pharmaceutical safety operations preferred
- Experience handling adverse event and signal detection activities preferred
Preferred Candidate Profile:
- Strong understanding of clinical safety and pharmacovigilance workflows
- Ability to work in collaborative global teams
- Excellent scientific and analytical mindset
- Strong communication and stakeholder management skills
- Ability to manage complex safety evaluations independently
- Experience working with regulatory authorities and safety boards preferred
Benefits of the Hybrid Pharmacovigilance Job:
- Opportunity to work with a global leader in generic and biosimilar medicines
- Exposure to advanced pharmacovigilance and drug safety operations
- Flexible hybrid work environment
- Career growth in pharmaceutical safety and regulatory sciences
- Opportunity to collaborate with global research and development teams
- Participation in international safety monitoring activities
- Inclusive and diversity-focused work culture
- Exposure to global healthcare and regulatory systems
- Professional growth in clinical safety leadership roles
- Opportunity to contribute to patient safety worldwide
