GCMA Associate

This role is integrated within the Global Gastrointestinal Category Medical Affairs team, responsible for medical sciences activities during the development and throughout the entire life cycle of RB products.

The post-holder is responsible for all relevant medical science activities under the guidance of the Global Category Medical Affairs Senior Manager, supporting our research, product development and medical strategy to deliver safe, efficacious, and meaningful solutions to consumers.

The position is accountable to the Global Category Medical Affairs Senior Manager, working closely with others across the medical sciences function and interacting as appropriate with other internal functions including Safety, Quality, Regulatory and Compliance (SQRC), R&D, Marketing, Professional Relations etc to drive commercial success.

With a broad remit, you'll support our research, product development and medical strategy.

• You'll support the investigation and substantiation of product claims for both advertising materials and regulatory submission, including creation of high-quality regulatory documentation.
• You'll interpret clinical and pre-clinical data accurately for the development of scientific manuscripts for publication.
• You'll deliver projects on time, on budget and to the appropriate success criteria / KPIs, whilst ensuring all technical work is completed to required procedures and standards.
• You'll provide support to advisor-level employees where appropriate.
• You'll effectively communicate and escalate to supervisor, cross functional teams and external partners.
• You'll build functional and technical knowledge alongside an awareness of current and future business requirements.
• You'll develop an understanding of the R&D operating model and identify ways to execute initiatives in accordance with it.

• You're qualified in healthcare or life sciences
• You're have good attention to detail which ensures excellent written communications.
• You understand clinical data, research methodology, information management and regulatory requirements across different product classifications
• You can demonstrate contribution to project delivery and collaboration.
• You have the ability to work efficiently, accurately and independently within a multi-discipilinary team.
• A good team player and proactive collaborator.
• You're have an ability to effectively prioritise and execute tasks under pressure.
• Desirable: good understanding and application of clinical statistics

Medical Affairs, Clinical Data, Research Methodology, Information Management and Regulatory Requirements R&D, Safety, Quality, Regulatory and Compliance (SQRC), Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes.