Alvotech Hiring Pharmacovigilance Associate – (Partially Remote Job)
- Alvotech Hiring Pharmacovigilance Associate – Drug Safety Jobs in Bangalore (Partially Remote)
- Company Overview
- Job Role and Responsibilities
- Core Responsibilities
- Eligibility and Qualifications
- Educational Qualification
- Experience
- Technical Skills
- Professional Skills
- Location and Salary
- Application Process
- Frequently Asked Questions
- What does a Pharmacovigilance Associate do?
- Who can apply for this pharmacovigilance job?
- What safety systems are commonly used in pharmacovigilance?
- Is this job suitable for freshers?
- Where is the job located?
- Job Summary
Alvotech Hiring Pharmacovigilance Associate – Drug Safety Jobs in Bangalore (Partially Remote)
Alvotech is inviting applications for the position of Pharmacovigilance Associate – Safety Data Management within its Global Safety and Clinical Research division. This opportunity is based in Bangalore with a partially remote work model and is ideal for professionals with experience in pharmacovigilance, drug safety monitoring, and clinical safety data management.
The vacancy is part of the Integrated Clinical and Medical Research (iCMR) department, which focuses on developing effective clinical strategies for biosimilar medicines and ensuring compliance with international regulatory standards. Candidates with 2+ years of experience in pharmacovigilance or clinical safety management and a postgraduate qualification in pharmaceutical sciences or life sciences are encouraged to apply.
This role offers an excellent opportunity to work in the rapidly growing biopharmaceutical and biosimilars industry, contributing to global drug safety monitoring and regulatory compliance activities that directly support patient safety worldwide.
Company Overview
Alvotech is a fully integrated biopharmaceutical company specializing in biosimilar development and manufacturing. The company focuses on delivering high‑quality biosimilar medicines that expand patient access to life‑saving treatments while reducing healthcare costs globally.
Headquartered internationally and operating across multiple global markets, Alvotech collaborates with pharmaceutical partners and regulatory agencies to bring safe and effective biosimilar therapies to patients.
Within the organization, the Integrated Clinical and Medical Research (iCMR) department leads the planning and execution of clinical trials, regulatory compliance strategies, and post‑marketing safety programs. The department aligns clinical development with global biosimilar guidelines and regulatory requirements issued by authorities such as the FDA, EMA, and international regulatory bodies.
By joining Alvotech, professionals gain the opportunity to work with advanced pharmacovigilance technologies, safety databases, and global clinical research programs supporting biologics and biosimilar therapies.
Job Role and Responsibilities
The Pharmacovigilance Associate – Safety Data Management will support clinical safety monitoring activities for both clinical trials and post‑marketing pharmacovigilance programs. The role focuses on maintaining accurate safety data, ensuring regulatory compliance, and supporting global drug safety operations.
The position operates within the Global Safety Data Management team and reports to the Safety Data Management Director.
Core Responsibilities
• Manage assigned pharmacovigilance tasks related to clinical trial safety and post‑marketing drug safety monitoring
• Handle Individual Case Safety Reports (ICSR) and Serious Adverse Event (SAE) management activities
• Support regulatory safety submissions to global health authorities
• Perform literature monitoring and digital safety surveillance for drug safety signals
• Conduct reconciliation activities between clinical safety databases and external partners
• Manage EudraVigilance (EV) and XEVMPD related activities where applicable
• Participate in the configuration, validation, and lifecycle management of pharmacovigilance systems
• Maintain and optimize global pharmacovigilance processes aligned with international regulations
• Ensure compliance with global pharmacovigilance standards including FDA, EMA, and ICH guidelines
• Collaborate with cross‑functional teams including clinical trials, regulatory affairs, quality assurance, and benefit‑risk management
• Coordinate with pharmacovigilance service providers and global business partners
• Deliver training programs related to pharmacovigilance processes and safety compliance standards
• Support internal and external audits and regulatory inspections related to safety data management
Through these responsibilities, the Pharmacovigilance Associate contributes to maintaining patient safety by ensuring accurate monitoring, reporting, and evaluation of drug safety information.
Eligibility and Qualifications
Candidates interested in the Pharmacovigilance Associate role should meet the following educational and professional criteria.
Educational Qualification
Master’s Degree in pharmaceutical sciences or related healthcare disciplines.
Relevant educational backgrounds include:
MPharmacy, MSc Pharmacology, MSc Clinical Research, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Life Sciences, PharmD, MSc Pharmaceutical Sciences, MSc Biomedical Sciences.
Experience
• Minimum 2 years of experience in pharmacovigilance or drug safety operations
• Hands‑on experience in clinical trial safety monitoring and post‑marketing pharmacovigilance activities
Technical Skills
• Experience working with pharmacovigilance safety databases such as Argus Safety, ARISg, or Veeva Safety Vault
• Knowledge of pharmacovigilance regulations including 21 CFR, ICH guidelines, GVP, GCP, and CIOMS standards
• Experience working with global pharmaceutical products and clinical trials
• Understanding of safety data management lifecycle and regulatory reporting requirements
• Familiarity with biologic or combination product safety monitoring is considered an advantage
Professional Skills
• Strong organizational and time‑management abilities
• Excellent written and verbal communication skills
• Ability to work independently and collaborate within multicultural teams
• Strong analytical skills for evaluating clinical safety data
• Ability to manage multiple pharmacovigilance tasks simultaneously in a dynamic environment
• Willingness to travel internationally when required
Professionals with experience in pharmacovigilance case processing, clinical safety data management, drug safety surveillance, and regulatory safety reporting will find this role highly aligned with long‑term careers in pharmaceutical safety science.
Location and Salary
Location: Bangalore, India
Work Model: Partially Remote / Hybrid
Application Process
Candidates interested in applying for the Pharmacovigilance Associate – Safety Data Management role can submit their application through the official Alvotech careers portal.
Apply Here:
Applicants should apply before March 23, 2026 to be considered for this position.
Frequently Asked Questions
What does a Pharmacovigilance Associate do?
A Pharmacovigilance Associate monitors drug safety information, processes adverse event reports, ensures regulatory compliance, and supports clinical trial and post‑marketing safety surveillance activities.
Who can apply for this pharmacovigilance job?
Candidates with a master’s degree in pharmacy, pharmacology, biotechnology, clinical research, or life sciences with at least two years of experience in drug safety or pharmacovigilance can apply.
What safety systems are commonly used in pharmacovigilance?
Common pharmacovigilance systems include Argus Safety, ARISg, and Veeva Safety Vault which help manage safety reports, regulatory submissions, and drug safety monitoring.
Is this job suitable for freshers?
No. This role requires at least two years of experience in pharmacovigilance or clinical safety operations.
Where is the job located?
The role is based in Bangalore, India, with a partially remote work model.
Job Summary
| Category | Details |
|---|---|
| Company | Alvotech |
| Vacancies | Pharmacovigilance Associate – Safety Data Management |
| Required Education | MPharmacy, MSc Pharmacology, MSc Clinical Research, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Life Sciences, PharmD, MSc Pharmaceutical Sciences, MSc Biomedical Sciences |
| Experience | Minimum 2+ years in Pharmacovigilance or Drug Safety |
To apply for this job please visit alvotech.wd103.myworkdayjobs.com.
