Senior Research Associate - ADME & Formulation

Let’s build the future of medicine—together.

Join Enveda as a SRA, Bioanalyst ADME & Formulation in Hyderabad, India and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation—are you ready to make a difference?

Hyderabad, India | Full-Time

What Makes Us Enveda

Life is smart, and we can learn from it. We’re reinventing drug discovery by harnessing nature’s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can’t wait.

What sets Enveda apart isn’t just what we do—it’s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day.

Our Momentum

• Unicorn status: Achieved following a $150 million Series D funding round in 2025
• Discovery and innovation: Advanced our first drug candidate to Phase 1 trials in 2024

Award-winning culture

• Newsweek: Top 100 Global #MostLovedWorkplaces (2025)
• Forbes: America’s Best Startup Employers (2024 & 2025)

Newsweek: America’s Greatest Startup Workplaces (2025)

LinkedIn: Top Startups to Watch (2024)

These milestones reflect the impact of our team and we’re just getting started, but they’re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you.

Your Role in Our Mission

At Enveda, every role drives impact. As a SRA in our DMPK department, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in bioanalytical methods will be critical in accelerating our mission to transform drug discovery because every breakthrough starts with bold questions and brave actions.

What You Will Do

• Run assays including CYP inhibition, kinetic and thermodynamic solubility, plasma protein binding, brain tissue binding, and microsomal/hepatocyte stability per Enveda SOPs and regulatory guidelines
• Conduct formulation feasibility studies and optimize formulations to support in vivo pharmacokinetic studies across multiple routes of administration
• Analyze and interpret experimental data; communicate findings clearly to the DMPK team and cross-functional stakeholders
• Plan, coordinate, and prioritize assay workload to meet turnaround time targets without compromising data quality
• Collaborate with medicinal chemists and pharmacologists to integrate ADME data into compound prioritization strategies
• Optimize and validate experimental protocols to ensure accuracy and reproducibility
• Stay current with industry trends and advancements in ADME science and formulation development

Who Will Thrive Here

The ideal candidate brings

• Master's degree in Pharmaceutical Sciences, Pharmaceutics, Formulation, Pharmaceutical Chemistry, or a closely related field
• 1–2 years of hands-on experience in DMPK or drug discovery in a research institute or pharmaceutical company
• Practical experience conducting one or more in vitro ADME assays: kinetic solubility, thermodynamic solubility, plasma protein binding, brain tissue binding, CYP inhibition, microsomal and/or hepatocyte stability
• Hands-on experience with formulation optimization for in vivo pharmacokinetic studies (preferred)
• Strong understanding of ADME properties, formulation science, and pharmacokinetics of small molecules