Clinical Project Lead for Real World Evidence studies
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Søborg
Do you want to join a large, committed global clinical operation area that plays a key role in ambitious and innovative drug development at Novo Nordisk? Are you motivated by bringing new innovative treatments to millions of patients worldwide and do you wish for a career in a global company offering great opportunities for personal and professional development? We are looking for a Clinical Project Lead to plan and drive innovative Real World Evidence studies within Rare Disease & Advanced Therapies. Read on and apply for a life-changing career! The position
As Clinical Project Lead for Real World Evidence (RWE) studies, you take on a senior role with extensive clinical project management responsibilities. You will be overall accountable for global RWE studies and initiatives and lead global cross functional study teams. You will be a key contributor and assume accountability for end-to-end planning and execution in collaboration with internal and external partners. You will be curious and contribute to innovative development of RWE data within Rare Disease & Advanced Therapies. Your responsibilities will also include:
• That study key deliverables are met on time, at a high quality and within budget by using your extensive project leadership competences
• Operational trial management processes including vendor management and oversight
• Being a proactive partner in internal and external partner collaborations
• Ample opportunity to influence our deliverables, improve our processes and identify novel ways of generating RWE data to the benefit of patients
Qualifications
To succeed in this role, you have:
• a MSc in Natural Science with at least five years of relevant experience or
• a BSc in Natural Science or equivalent with at least seven years of relevant experience (e.g., CRA, Global Trial Manager)
• Extensive clinical operational experience preferably with studies with RWE elements e.g. pragmatic trials, non-interventional studies and/or observational disease area studies
• Strong clinical project management expertise and the ability to independently impact and influence the execution and improvement of RWE processes
• Experience from cross-functional organizational work representing trial management views
• Experience in setting up and collaborating with external academic partners
• Curious mindset and innovative approach to plan and conduct RWE studies and initiatives
• Strong people and leadership skills, excel in stakeholder management and strong communication
Visit our Clinical Operations webpages:
If you are curious to know more about Clinical Operations in Novo Nordisk, the different positions, job content and qualifications, then please have a look here. We know it can be difficult to grasp the true sense of a role by reading a job add, so if your curiosity is triggered, we encourage you to give us a call, either to the hiring manager or to the RWE Specialist CPL in our area. About the project area
In our project area we cover the entire spectrum of clinical activities within the Rare Disease & Advanced Therapies area from early phase 1 trials to larger phase 3a programs and phase 3b/4 life cycle management activities on our marketed products. On RWE studies we work in close collaboration with our affiliates, CROs and external partners.
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 necessary 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
If you would like further information about the position, please contact Director Johanna Mercke Odeberg phone +4530759759 or email [email protected], or RWE expert CPL Eik Dybboe Bjerre, phone +45-30777482 or email [email protected] Deadline
8 March 2024, but screening and interviewing will be done on an ongoing basis.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. We are committed to an inclusive recruitment process and equality of opportunity for all our job applicants. 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.
As Clinical Project Lead for Real World Evidence (RWE) studies, you take on a senior role with extensive clinical project management responsibilities. You will be overall accountable for global RWE studies and initiatives and lead global cross functional study teams. You will be a key contributor and assume accountability for end-to-end planning and execution in collaboration with internal and external partners. You will be curious and contribute to innovative development of RWE data within Rare Disease & Advanced Therapies. Your responsibilities will also include:
• That study key deliverables are met on time, at a high quality and within budget by using your extensive project leadership competences
• Operational trial management processes including vendor management and oversight
• Being a proactive partner in internal and external partner collaborations
• Ample opportunity to influence our deliverables, improve our processes and identify novel ways of generating RWE data to the benefit of patients
Qualifications
To succeed in this role, you have:
• a MSc in Natural Science with at least five years of relevant experience or
• a BSc in Natural Science or equivalent with at least seven years of relevant experience (e.g., CRA, Global Trial Manager)
• Extensive clinical operational experience preferably with studies with RWE elements e.g. pragmatic trials, non-interventional studies and/or observational disease area studies
• Strong clinical project management expertise and the ability to independently impact and influence the execution and improvement of RWE processes
• Experience from cross-functional organizational work representing trial management views
• Experience in setting up and collaborating with external academic partners
• Curious mindset and innovative approach to plan and conduct RWE studies and initiatives
• Strong people and leadership skills, excel in stakeholder management and strong communication
Visit our Clinical Operations webpages:
If you are curious to know more about Clinical Operations in Novo Nordisk, the different positions, job content and qualifications, then please have a look here. We know it can be difficult to grasp the true sense of a role by reading a job add, so if your curiosity is triggered, we encourage you to give us a call, either to the hiring manager or to the RWE Specialist CPL in our area. About the project area
In our project area we cover the entire spectrum of clinical activities within the Rare Disease & Advanced Therapies area from early phase 1 trials to larger phase 3a programs and phase 3b/4 life cycle management activities on our marketed products. On RWE studies we work in close collaboration with our affiliates, CROs and external partners.
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 necessary 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
If you would like further information about the position, please contact Director Johanna Mercke Odeberg phone +4530759759 or email [email protected], or RWE expert CPL Eik Dybboe Bjerre, phone +45-30777482 or email [email protected] Deadline
8 March 2024, but screening and interviewing will be done on an ongoing basis.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. We are committed to an inclusive recruitment process and equality of opportunity for all our job applicants. 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 "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 15.2.2024, 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.
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|---|---|
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