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Cliantha Research, a globally recognized Contract Research Organization (CRO), is seeking an experienced Lead PK Scientist to join our team in Ahmedabad, India. With a strong focus on clinical research, bioequivalence (BA/BE) studies, and pharmacokinetics, we offer a dynamic environment for professionals passionate about advancing drug development. Be part of our mission to deliver high-quality clinical research solutions!
Why Cliantha Research?
Cliantha Research is a trusted name in clinical trials, known for compliance with ICH-GCP, USFDA, and EMA guidelines. Our Ahmedabad facility provides cutting-edge opportunities in pharmacokinetics and scientific affairs. Join us to work on innovative projects, collaborate globally, and grow your career in a supportive, high-impact environment.
Job Details
- Position: Lead PK Scientist
- Location: Ahmedabad, India
- Qualification: M. Pharm in Pharmacology
- Experience: 10–15 years in Pharmacokinetics and Scientific Affairs
- Application: Send resume to mjunnarkar@cliantha.com or dmirchandani@cliantha.com
Key Responsibilities
- Design, review, and interpret pharmacokinetic (PK) study data to support regulatory submissions
- Lead scientific strategy for bioequivalence (BA/BE) studies
- Mentor and train junior scientists to build a strong research team
- Collaborate with cross-functional teams to ensure compliance with global regulatory standards
- Prepare protocols, reports, and documentation for clinical trials and regulatory filings
- Analyze PK data using tools like Phoenix WinNonlin® for non-compartmental analysis
- Contribute to innovative approaches in drug development and clinical research
Why Join Us?
At Cliantha Research, you’ll work with a globally recognized team dedicated to excellence in drug development. Our collaborative environment fosters innovation and professional growth. With a strong presence in India, USA, and Canada, we offer opportunities to engage in high-impact clinical research projects.
Qualifications and Skills
- Educational Requirement: M. Pharm in Pharmacology
- Experience: 10–15 years in pharmacokinetics, with expertise in BA/BE studies and regulatory submissions
Skills:
- Strong understanding of PK modeling and bioanalytical methods
- Proficiency in statistical analysis and tools like Phoenix WinNonlin®
- Experience with clinical trial protocols and regulatory guidelines (e.g., USFDA, EMA)
- Leadership and mentoring abilities
- Excellent communication and collaboration skills
How to Apply
Ready to lead impactful pharmacokinetic research? Send your updated resume to mjunnarkar@cliantha.com or dmirchandani@cliantha.com. Learn more about our work at Cliantha Research.
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Be Part of Our Vision
Join Cliantha Research to drive innovation in clinical pharmacokinetics and contribute to global drug development. Apply now and take the next step in your career with a leading CRO committed to excellence!