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At Reckitt, we're looking for an insightful Senior Associate in Category Medical Affairs to join our innovative R & D team. You're not just providing scientific support you're shaping the future of consumer wellbeing with every project you touch. With your expertise, you'll ensure our products are not only effective but backed by sound science and regulatory compliance. If you're ready to take on a role where your strategic thinking and eye for detail will lead to real-world impact, then we are excited to meet you.
Role/ Purpose
. To provide expert statistical input across the portfolio of work for EG&CR including but not limited to evidence brief, protocol, SAP, topline and CSR using consumer insights to meet business needs
. To select and work efficiently and effectively with outsourcing partners ensuring high quality deliver on time to agreed costs
. To provide data generation know how across the business as required
Scope of Role
. Provide execution of analysis based on primary and secondary use data across the portfolio, supporting the Manager of Statistics
Serve as a leading figure within the Medical Sciences team, actively contributing to our cross-functional project successes.
- Balance commercial insights with scientific rigour to drive the business forward while upholding compliance.
- Establish key external partnerships that reinforce our category initiatives and help navigate product classification strategies.
- Interpret data thoughtfully to provide meaningful insights, encouraging innovative solutions that resonate with our consumers.
- Guide our claim development and defence, setting the bar high for industry standards.
- Embody change leadership and champion continuous improvement across medical affairs to enhance our practises.
Accountabilities
. The role is responsible for individual excellence in a team setting to design and deliver the innovation portfolio as well as develop sound statistical thinking in the wider Reckitt medical team and beyond.
Key Challenges
. Provide expert statistical input to the portfolio of work ensuring scientifically robust evidence generation activities are integrated into the project (e.g. innovative approaches such as methods, models and techniques to achieve claims and end points).
. Deliver key evidence supporting product claims and registration.
. Collaborate and integrate expertise from EG&CR and Medical Affairs to incorporate clinical endpoints, comparators etc
. Assist in efforts to identify, integrate, and/or develop valid clinical outcome assessments (PRO/COA) measurements for use in clinical programs.
OVERSIGHT
Compliance and adherence to SOPs:
. Compliance with necessary regulations for quality and disclosure.
. Input into and ownership of relevant standard operating procedures.
. Ensure best practices and consistency within the team.
- Skilled at interpreting scientific and clinical data, with a knack for detail-oriented document preparation.
- Adept at developing strategic partnerships and engaging with industry bodies.
- Forward-thinking in compliance and regulation, with a strong understanding of its business impact.
- Capable of managing relationships and leading through change, with an eye on consumer insights and creative direction.
- Open to adopting new technologies and challenging the conventional to foster improvement.
Professional Qualification/Experience
. BSc in a numerate degree and experience in a clinical trial setting
. MSc in a statistical/numerate degree with good knowledge of medical statistics.
Reckitt Benckiser (India) Ltd. 6th & 7th Floor, Tower C, DLF Cyber Park, 405 B, Udyog Vihar Phase III, Sector 20, Gurgaon 122016, Haryana.
Job ID: 150197129
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