VP, Research & Development
Role Overview
Reporting to the President & Chief Executive Officer (CEO) and the Global Head of R&D, the Head of Research & Development (R&D) will play a lead role in delivering business critical R&D programmes.
The Head of R&D is a member of the Molecular Imaging Senior Leadership Team and will have management responsibility for the following functions: Biometrics; Chemistry, Manufacturing & Control (CMC); Clinical Operations; Editorial (Medical Writing); Imaging; Non-Clinical; R&D Programme Management
Full Job Posting
Job purpose
- Reporting to the President & Chief Executive Officer (CEO) and the Global Head of R&D, the Head of Research & Development (R&D) will play a lead role in delivering business critical R&D programmes. The Head of R&D is a member of the Molecular Imaging Senior Leadership Team and will have management responsibility for the following functions: Biometrics; Chemistry, Manufacturing & Control (CMC); Clinical Operations; Editorial (Medical Writing); Imaging; Non-Clinical; R&D Programme Management
- Main Responsibilities, Activities, Duties and Tasks
- Biometrics (to include biostatistics, statistical programming, and data management), ensuring operational delivery and the provision of strategic advice concerning statistical methods and data management activities.
- Chemistry, Manufacturing & Control (CMC) ensuring the robust manufacturing and supply of materials used in the manufacture of investigational and finished commercial radiopharmaceutical products.
- Clinical operations, ensuring operational delivery and the provision of strategic advice concerning the design, feasibility and execution of all clinical studies.
- Editorial (medical writing), ensuring the development and implementation of strategic publication plans and the dissemination of scientific and clinical data (e.g., via manuscripts and conference presentations).
- Imaging, providing medical physics support, including radiation physics, medical imaging physics and imaging analytics expertise.
- Non-clinical, to include evaluations of non-clinical toxicology, safety and efficacy.
- R&D programme management, including:
- Delivery of the programme strategy (in accordance with the Long-Range Plan and in close collaboration with colleagues in Clinical Development, Commercial, Finance, Innovation & Strategy, Legal (incl. Intellectual Property), Medical Affairs, Pharmacovigilance & Quality and Regulatory Affairs).
- Operational oversight and project delivery, in compliance with applicable laws, industry codes and regulations
- Budget management (including Long-Range Planning, Annual Budget and Rolling Forecast 2 & 3 and related resource allocation & planning),
- Portfolio review,
- Risk management,
- Regular reporting to the Executive Committee and Board of Directors including progress in achieving strategic objectives; advising of any significant variance from the approved strategic plans and budget; and any significant programme issues.
- Research and Development
- Collaborating with the New Asset Evaluation Team, specifically on the identification and technical assessment of new licensing, lifecycle and geographic expansion opportunities.
- Collaborations with academia, pharma and imaging equipment providers
- All matters of significant organisational structure within R&D, including development of the capabilities of the internal workforce and the recruitment, promotion, retention, succession planning & dismissal of employees, in conjunction with Human Resources.
- Establish or implement departmental policies, goals, objectives, or procedures in conjunction with the Leadership Team and Global R&D at Bracco.
- Other duties as determined by business needs
- Education/Qualifications
- Educated to at least degree level, preferably with a PhD in science or life science (or
- equivalent research experience)
- Professional Experience, Knowledge, & Technical Skills
- Significant experience in clinical drug development and particularly the development of medical imaging agents and radiopharmaceuticals is key, as is significant experience of staff & performance management.
- A strong scientific background in a relevant area in a relevant scientific discipline an advantage and awareness of relevant guidelines and regulations governing drug development activities, particularly imaging drugs, a pre-requisite.
- Knowledge of Regulatory Authority (i.e., EMA, FDA) and Good Clinical Practice (GCP) guidelines.
- Proven leadership, organisational, facilitation, negotiation, collaboration, empowerment, and interpersonal skills with the ability to work effectively with others at all levels of the organisation.
- Experience with cross-functional and highly matrixed organizations.
- Ability to coach, mentor, develop and educate direct reports.
- Excellent written and verbal communication
- Soft Skills – Company Values & Behaviours
- Excellent interpersonal skills, including communication verbally and in writing. Ability to influence and build relationships in a global organisation
- Excellent organisational skills, including multitasking, efficiency, punctuality, and project management
- Excellent collaboration skills including experience in a cross-functional and highly matrixed organisation.
- Contract type:
- If you meet the requirements of this opportunity and would like to join an international group working to improve patients' lives, apply now!
- At Bracco, we believe in the values of diversity and inclusion. We respect and celebrate the diversity of our people and their experiences, ensuring a fair opportunity for all.
- We are #Bracco #JoinUs
About Bracco Imaging
Family-owned diagnostic imaging company developing contrast agents, medical devices, and imaging solutions for healthcare professionals and patients.
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