At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering
an environment where you grow at every step, take charge of your journey and
thrive in a supportive community.
ARE YOU READY TO CREATE YOUR OWN SUNSHINE?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every
day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and
lead with confidence. Additionally, demonstrate a collaborative spirit, knowing
that we ‘Thrive together’ and support each other’s journeys.”
Job Description:
1. Literature search and study designing of Bioavailability and Bioequivalence
studies of oral & non-oral products towards different regulatory submission.
2. Review of BA/BE study protocol and provide Pharmacokinetic (PK) inputs into
the study protocols
3. Coordinate with the CRO in India and outside India for finalizing biostudy
pilot and pivotal study protocol for DCGI BE application.
4.
Develop protocol for patient based BA/BE studies & PD end point study for
complex generics.
5. Perform PK and Statistical analysis of in-vivo data obtained from BA/BE and
pharmacokinetics studies using Phoenix Software.
6. Literature search and study designing of Bioavailability and Bioequivalence
studies of oral & non-oral products towards different regulatory submission.
7. Review of BA/BE study protocol and provide Pharmacokinetic (PK) inputs into
the study protocols
1.
Travel Estimate
NA
Job Requirements
Educational Qualification
M.Pharm
Experience
Tenure: 4-6 years
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities We provide
robust perks and opportunities to foster personal and professional growth.
Join us at Sun Pharma, where every day is an opportunity to grow, collaborate,
and make a lasting impact. Let’s create a brighter future together