Job Description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Benefit/Risk Associate based in India.

This is an excellent opportunity for recent graduates and early-career professionals to begin a meaningful career in pharmacovigilance and drug safety. The role focuses on supporting benefit-risk assessments and signal detection activities that contribute directly to patient safety and regulatory compliance across global healthcare programs. You will work within collaborative international teams, gaining exposure to a wide variety of clinical and post-marketing projects while developing specialized expertise in pharmacovigilance processes. The position offers continuous learning opportunities, hands-on experience with safety data analysis, and the chance to contribute to critical healthcare decisions. It is ideally suited for individuals who are detail-oriented, scientifically curious, and motivated by making a positive impact on patient outcomes worldwide.

Accountabilities:
  • Support signal detection activities, including process setup and ongoing pharmacovigilance operations.
  • Review safety data and line listings to assist in the identification and evaluation of potential safety signals.
  • Draft and contribute to signal detection reports while ensuring accuracy, completeness, and quality standards.
  • Perform quality control activities related to benefit-risk documentation and pharmacovigilance deliverables.
  • Maintain accurate records, tracking tools, and documentation in accordance with internal procedures and regulatory requirements.
  • Collaborate with cross-functional teams to ensure signal management activities are conducted efficiently and compliantly.
  • Contribute to the continuous improvement of pharmacovigilance processes and operational practices.
  • Ensure all assigned activities are completed within established timelines and quality expectations.
  • Requirements

    • Bachelor's degree in Life Sciences, Biomedical Sciences, Pharmacy, Biotechnology, Chemistry, Biology, Veterinary Science, or another healthcare-related discipline.
    • Previous professional experience is not required, making this an ideal opportunity for recent graduates and early-career professionals.
    • Strong interest in pharmacovigilance, drug safety, and patient-focused healthcare initiatives.
    • Excellent organizational skills with the ability to manage multiple priorities and maintain strong attention to detail.
    • Strong analytical thinking and problem-solving capabilities.
    • Effective interpersonal and communication skills, with the ability to work collaboratively in international and multicultural environments.
    • Good time management and multitasking abilities.
    • Proficiency in written and spoken English, with a minimum level equivalent to B2 or above.
    • Proactive mindset, eagerness to learn, and commitment to delivering high-quality work.
    • Benefits

      • Opportunity to launch and develop a long-term career in pharmacovigilance and drug safety.
      • Exposure to diverse projects ranging from clinical trials to large-scale post-marketing activities.
      • Comprehensive training and continuous professional development opportunities.
      • Collaborative and supportive international work environment.
      • Meaningful work contributing directly to patient safety and public health outcomes.
      • Inclusive culture that values diversity, teamwork, and individual contributions.
      • Opportunities to work with experienced professionals across global healthcare and life sciences sectors.
      • Dynamic environment that encourages learning, growth, and career progression.
      • Flexible and people-focused workplace culture designed to support employee wellbeing and professional success.