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Associate, Patient Safety & Experience Job at Alcon – Apply Now!

Published on

Alcon

2 - 5 Years

Bangalore

M.Pharm, Msc in Pharmacology or Biotechnology, M.Tech in Biotechnology or Biomedical Engineering, Ph.D in Pharmacology, Pharmaceutical Sciences, Biotechnology, or a related discipline

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Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Are you passionate about advancing drug development and patient safety? Alcon, a global leader in medical devices, is hiring an Associate II, Patient Safety & Experience in Bangalore, India. This exciting full-time role offers a chance to work on cutting-edge pharmacokinetic and pharmacodynamic (PK/PD) research while collaborating with R&D teams to shape the future of healthcare innovation. If you’re detail-oriented, skilled in decision-making, and ready to make an impact, this job is for you!

What You’ll Do in This Role

As an Associate II, you’ll dive into the world of model-based drug development (MBDD), using mathematical and statistical tools to evaluate compounds and enhance clinical trial efficiency. Here’s a snapshot of your responsibilities:

  • Analyze pharmacokinetic/pharmacodynamic (PK/PD) characteristics, including absorption, distribution, metabolism, and excretion (ADME).
  • Leverage empiric, mechanistic, and population modeling to assess drug variability in non-clinical and clinical stages.
  • Collaborate with R&D partners to support molecule selection, dosing strategies, and Phase II/III clinical trial designs.
  • Implement innovative trial designs to improve decision-making and streamline drug development processes.
  • Ensure compliance with national and international medical device regulations and safety guidelines.

This role is perfect for professionals who thrive in fast-paced environments and want to contribute to groundbreaking healthcare solutions.

Key Skills & Qualifications

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Alcon is looking for candidates who bring both technical expertise and strong interpersonal skills. Here’s what you need:

  • Excellent communication and listening skills to collaborate effectively with teams.
  • Strong decision-making and negotiation abilities to manage complex projects.
  • Ability to multitask, prioritize, and maintain attention to detail under tight deadlines.
  • Knowledge of medical device safety, vigilance, and regulatory guidelines (pre- and post-marketing).
  • Basic proficiency in MS Office for documentation and analysis.

A background in pharmacokinetics, pharmacodynamics, or medical device development is a plus!

Application Link

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