Entry level role supporting Global Safety Physicians and PV Scientists with safety data review, identifying/escalating safety issues, and drafting safety documents and regulatory reports.
Responsibilities
Supports proactive pharmacovigilance and risk management planning for designated products
Project managing preparation of the safety aspects of the global Risk Management Plans
Provides patient safety input to pivotal study documents like Investigator Brochures, Protocols, Informed Consents and Clinical Study Reports
Runs/supports routine signal detection processes
Identifies and uses appropriate sources of information and database searches to retrieve relevant data for evaluation of signals
Lead and support clinical development activities for late phase AstraZeneca-sponsored clinical programs, including protocol design, data review, safety monitoring, and regulatory submissions.
Locations (2)
Manyata Tech Park, Bangalore, India
Bangalore, India
Responsibilities
Draft and review clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other Health Authority submissions
Implement protocols and interact with vendors and CROs
Produce materials for investigator meetings
Triage and address questions regarding scientific and protocol procedures
Serve as contact with vendors and CROs regarding medical/clinical science issues
Requirements
Required Life Sciences degree or equivalent
PharmD with equivalent experience, Ph.D. degree in life sciences, or MD preferred
Nice to have: Oncology experience
Nice to have: Industry or academic experience in drug development
Principal Medical Science Liaison - Rare Epilepsies
The Principal MSL provides advanced, field-based medical and scientific leadership in support of Lundbeck’s NeuroRare focus on developmental and epileptic encephalopathies, serving as a strategic pre-launch scientific partner to external experts.
Locations (8)
Northeast, Northeast, United States
Mid-Atlantic, Mid-Atlantic, United States
Southeast, Southeast, United States
Texas, Texas, United States
Central Gulf, Central Gulf, United States
Principal Medical Science Liaison - Rare Epilepsies
The Principal MSL provides advanced, field-based medical and scientific leadership in support of Lundbeck’s NeuroRare focus on developmental and epileptic encephalopathies, serving as a strategic pre-launch scientific partner to external experts and internal stakeholders.
Pacific Northwest, Pacific Northwest, United States
Show all 8 locations
Upper Midwest, Upper Midwest, United States
Great Lakes, Great Lakes, United States
Compensation
Salary Pay Range: $215,000 - $245,000 and eligibility for a 20% bonus target based on company and individual performance, and eligibility to participate in the company’s long-term incentive plan.
Responsibilities
Establishishes and sustains deep, longitudinal scientific partnerships with Key Opinion Leaders (KOLs), Centers of Excellence, and investigators.
Serves as a trusted scientific expert through high-quality, compliant scientific exchange that advances understanding of disease biology, unmet need, endpoints, and emerging evidence.
Acts as a primary generator of pre-launch actionable field medical insights by systematically testing scientific value narratives, differentiation hypotheses, and evidence gaps.
Synthesizes and communicates high-quality insights with clear implications for evidence strategy, publication planning, disease education, and portfolio-level decision-making.
Ensures timely, accurate, and compliant documentation of insights in CRM systems.
Requirements
Accredited advanced degree in a health or life sciences–related field
Salary Pay Range: $215,000 - $245,000 and eligibility for 20% bonus target based on company and individual performance
Responsibilities
Estishes and sustains deep, longitudinal scientific partnerships with Key Opinion Leaders (KOLs), Centers of Excellence, and investigators.
Serves as a trusted scientific expert through high-quality, compliant scientific exchange advancing understanding of disease biology, unmet need, and emerging evidence.
Acts as a primary generator of pre-launch actionable field medical insights by testing scientific value narratives and differentiation hypotheses.
Synthesizes and communicates high-quality insights for evidence strategy, publication planning, and portfolio-level decision-making.
Leads or co-leads cross-functional workstreams across Medical Directors, Clinical Development, and Evidence Strategy.
Requirements
Accredited advanced degree in a health or life sciences–related field (MD, DO, PharmD, PhD, NP, PA, or Master's)
Nice to have: Rare disease experience
Nice to have: Developmental and epileptic encephalopathies expertise
Nice to have: Epilepsy knowledge
Nice to have: Pediatric neurological disorders experience