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Senior Clinical Research Associate
Senior Clinical Research Associate-September 2024
Mumbai
Sep 8, 2025
About Senior Clinical Research Associate

   ABOUT UNILEVER:

  Be part of the world's most successful, purpose-led business. Work with brands that are well-loved around the world, that strive to improve the lives of our consumers and the communities around us every day. Every day, nine out of ten Indian households use our products to feel good, look good and get more out of life - giving us a unique opportunity to build a brighter future. We promote innovation, big and small, to make our business win and grow; and we believe in business as a force for good. Our brilliant business leaders and colleagues provide mentorship and inspiration, so you can be at your best.

  At HUL, we believe that every individual irrespective of their race, color, religion, gender, sexual orientation, gender identity or expression, age, nationality, caste, disability or marital status can bring their purpose to life. So, apply to us, to unleash your curiosity, challenge ideas and disrupt processes; use your energy to make the world a better place. As you work to make a real impact on the business and the world, we'll work to help you become a better you!

  We are looking to hire a Clinical Research Associate/ Sr. Clinical Research Associate in our Beauty & Wellbeing team based in Mumbai.

  Background & Job description:

  Clinical research area is a strategic Capability for Unilever Research & Development (R&D). The Clinicals team at Mumbai is seeking a Clinical Research Associate to support Oral Care clinical programs.

  The role involves leading clinical studies from communication (internal/external/CROs), study design, documentation, coordinating with third parties for clinical study execution, study monitoring for compliance, and study reporting. Responsible for full delivery of the studies supporting Oral Care R&D teams across geographies within agreed timelines and budgets.

  Main Responsibilities of Project Management:

  Independent full clinical project management skills in delivering the study on time in full (OTIF) and within budget. Ability to identify and flag potential issues and associated risks to Clinicals Manager/Global Clinical Leader. Proactively communicate with project team and within clinicals on clinical study all elements. Effective coordination of all activities with third parties to conduct clinical studies and reporting. Engage with cross functional teams to understand requirements (clinical) with project teams and suggest suitable action/study design. Capture all relevant data, interpret, and write the clinical study reports.

  Others:

  This role will require innovative and creative thinking, as well as personal drive for clinical study execution. Able to adapt to changing needs of project and/or business. Knowledge of clinical design and a broad science base; oral biology would be added advantage. Ability to recognize significance of unusual test results and how they lead to new clinical insights and technical opportunities; ability to handle & interpret data and communicate significance of what it means to teams. Fundamental knowledge of claim support.

  Relevant Experience:

  Bachelors or Master's degree in biological or dental sciences (or comparable) with minimum 2-3 (upto 4-5) years of experience in Personal Care category/FMCG experience or equivalent relevant work experience within a clinical setting.

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