Code Review Manager

Bristol Myers Squibb ,
Uxbridge, Greater London
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Overview

Job Description

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. Job Purpose The Code Review Team forms an integral part of the Bristol-Myers Squibb Medical Affairs department, acting as a specialised hub for ABPI and IPHA Codes of Practice knowledge and Copy Approval expertise. As a Code Review Manager, you will actively collaborate with cross-functional teams (including Commercial, Medical, Regulatory, Pharmacovigilance, Access, and Policy, Advocacy and Government Affairs), to help support the brand, define projects from concept through their development, and be responsible for the compliant and timely review, examination, and certification of both promotional and non-promotional materials and activities. With the challenge of working in one or more dedicated therapy areas and multi-indication products, you will be encouraged to find and drive innovative solutions in the business and help teams skilfully navigate challenges to ensure compliance. Key Responsibilities: * To support the review process and act as a final signatory for the ABPI and IPHA Codes of Practice, ensuring compliance for all promotional and non-promotional materials, activities, and meetings * To work cross-functionally, connecting with multiple internal stakeholders within the organisation, to support the execution of an integrated strategic medical and tactical plans * To ensure business outputs are of a professional quality and that high standards are always maintained * Integrate into a highly efficient, professional and cohesive copy approval team * Partner with the outsourced data accuracy resource team to coordinate priorities and work load, ensuring business needs are always met * To proactively support the Code Governance Manager to assist with training and mentoring of new ABPI signatories, and support on-going company-wide training in all applicable Codes * Demonstrate personal commitment to on-going learning; through attendance at external conference, code fora and workshops, and sharing those learnings internally with the wider signatory matrix * Continue to shape the compliant company culture, by finding new ways to drive forward compliance with all relevant local and international Codes of Practices (IFPMA, EFPIA etc), whilst abiding to business strategy, and company policies and procedures * Identify, plan and implement innovative solutions to business and compliance challenges Candidate profile: Looking for an energetic and proactive individual, with a solution-orientated mindset. Must be agile, flexible and adaptable to a fast-paced role. Must be able to demonstrate sound judgement and accountability in relation to compliance-related decision-making. Will be able to multi-task and manage multiple on-going projects, whilst delivering to tight timelines. Excellent communication skills to enable cross-functional working. Must have a focused mindset and be willing to constantly learn and develop. Must be able to demonstrate excellence in quality and deliver to high standards. Knowledge & Skills: * Ability to understand and negotiate the needs of the commercial and medical teams together with the purpose and application of the Code and BMS policies, to enable the release of compliant, ethical and impactful materials * Ability to establish effective, strong and productive working interfaces with relevant stakeholders, leveraging both formal and informal networks to deliver; * An excellent understanding of country and therapy area specific regulations and guidelines, and broad knowledge of the UK healthcare system * Deep scientific understanding to analyse and dissect in depth scientific data; * Requires Computer Literacy, Strong written and Verbal Communication Skills; * Ability to work within complex cross-functional people matrixes, with differing priorities; * Multitasking and Commitment to delivery to hard deadlines, * Must be decisive to make bold decisions independently, sometimes in ambiguous circumstances, and be able to communicate in difficult and high pressured situations; * Must be able to prioritise workload and ensure business continuity Qualifications: * Required to be a GMC registered medic or a GPhC registered pharmacist * ABPI Final Signatory Experience Experience: Core * Must have significant ABPI Final Signatory Experience * Must have a scientific background to be able to interpret and appraise clin

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