Senior Product Director- Clinical Operations
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Søborg
Do you enjoy making a high impact at a strategic level and strive to deliver great results? Are you a strong communicator who is able to effectively navigate complex, cross-cultural discussions across Senior Vice President (SVP) Areas? Are you ready to take Risk Based Quality Management to the next level in Development? Then this is your chance to take your next challenge and be our new Senior Product Director for Risk Based Quality Management (RBQM) in Clinical Drug Development. Apply today! The position In the role as Senior Product Director for RBQM, you will be responsible for developing and executing the RBQM project plan involving processes, procedures, people, and application of digital solutions to ensure RBQM is taken to the next level. You will be supported by a team of Project Managers from different SVP areas across Development who coordinate, develop and roll out new ways of working. This is to ensure a consolidated Risk Based approach in how we setup and monitor our studies across skill areas. You will also set direction in how to train and coach the employees involved in studies from Line of Business (LoB) managers to trial squad members to fulfil RBQM goals. Your key responsibilities include: Drive the Novo Nordisk strategy for RBQM across all involved skill areas: RBQM scope, goals, expected deliverables, and stakeholders, and ensure alignment with corporate objectives and priorities, and LoB leadership Build, prioritize and maintain the development plan, roadmap, and backlog, including on top industry standards and regulatory authorities’ position Show excellence in finding synergies with other functions, secure proper alignment, and identify risks Lead and challenge relevance and impact of defined goals, and fit with existing and upcoming regulation Ensure delivery according to agreements, guarantee organizational readiness and implementation, and challenge the status-quo to further optimize resources and improve quality Ensure high visibility of RBQM project, lead and continuously improve the way project outcomes are shared, how they impact the organization (from global to local and across functions), and take action upon it Furthermore, you will work with the RBQM Leadership on a daily basis overcoming challenges and clarifying questions to ensure flow. Qualifications To thrive and succeed, we expect you to have: Master’s degree or bachelor’s degree in science Solid understanding and +8 years experience working with Clinical Trial execution and/or monitoring and operational aspects of planning and conducting global clinical trials Proven track record working in a project-oriented and international matrix organisation with strong business insight and knowledge Fluency in English You have the ability to inspire and motivate employees to do their best. You communicate a compelling purpose and vision with passion and translate strategy into ambitious goals with clear priorities. You can make bold decisions and take risk, seek new and innovative solutions and demonstrate ability and willingness to adjust quickly to new situations in a continuously developing environment. Additionally, you have a proactive mind-set and ability to work independently in a continuously developing environment. You possess proven strong analytical skills, are well organised, and have solid problem-solving capabilities. You can keep your spirits high even when under pressure, and can collaborate at any organisational level. About the department The Senior Product Director for RBQM is based in the Clinical Operations Centre of Expertise anchored in Trial Portfolio Management and Innovation (TPM&I) in Clinical Drug Development. We work closely with all other skill areas in Clinical Drug Development, e.g. Trial Management, Data Management, Clinical Pharmacology, Biostatistics, Clinical Reporting, Medical & Science as well as with our Clinical Drug Development Global Business Services in India, and our global Clinical, Medical & Regulatory organisation. Overall, the TPM&I area consists of approximately 250 highly skilled people based in Denmark and India, responsible for providing strategic leadership in the areas of Medical & Science, Clinical Operations, Global Trial Effectiveness, Vendor Management, Process Improvements and Compliance. In Clinical Drug Development, we are responsible for managing clinical drug development worldwide from early development phases to product launch. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Bo Maach-Møller +45 3079 5437. Deadline 31 January 2023. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 23.12.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forretningsudvikler
- Søborg
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