Clinical Project Manager
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Job Summary
Title:
Clinical Project ManagerCompany:
Ipsen Pharma (SAS)About Ipsen:
Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs in the U.S. France and the U.K we tackle areas of high unmet medical need through research and innovation.
Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration excellence and impact. At Ipsen every individual is empowered to be their true selves grow and thrive alongside the companys success. Join us on our journey towards sustainable growth creating real impact on patients and society!
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Job Description:
Are you ready to lead and innovate in a dynamic patient-focused biopharmaceutical company
Ipsen is a growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients health and quality of life providing effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology Neurosciences and Rare Diseases.
Why Ipsen
Patient-Focused: The patient is at the heart of everything we do and improving their outcomes is the deliverable of every strategy.
Employee Care: We care for our employees who are the ambassadors making a real difference.
Bold Leadership: We attract and develop bold agile entrepreneurial individuals who take full ownership of their decisions.
Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast-moving game-changing organization.
About the Role
The Clinical Project Manager (CPM) is a Project Leader with the end to end accountability for the successful execution of global Evidence Generation activities.
Main Responsibilities
- Planning initiating conducting and reporting for all assigned evidence generation projects
- Where activities are outsourced this means oversight of the Service Provider (SP) and co-ordination of internal cross functional team (CFT) if in house then this is undertaking the activities personally and coordinating the deliverables of the internal CFT.
- Responsible for activities/task packages delegated to you for projects assigned and/or take accountable for own projects (smaller and/or less complex projects).
Preparation of the study
- Set-up and lead the study Cross Functional Team (CFT) overseeing study design and kick-off activities. - Initiate high level feasibility and continuously monitor how changes to the study design affect feasibility during the preparation and development of the study protocol.
Initiation of the study
- Lead the SP selection process (RFP creation bid defense contracting) and in collaboration with the CFT Global Procurement and Corporate Legal Affairs.
- Co-ordinate completion of the study Integrated Oversight Plan (IOP) prior to initiation of the study defining and agreeing KPIs/QTLs/Performance indicators with SPs and the Cross Functional Team.
- Oversee SP performance and creation of documents required for the execution of the study
Study Conduct
- Coordinate the CFT (internal and SPs) overseeing the progress of the study and SPs performance to ensure timely on budget delivery.
- Monitor execution and delivery of KPIs/QTLs/Performance indicators as agreed in the IOP.
- Provide and present regular reports on study progress including site performance data quality and resource needs.
Study Completion
- Coordinate the preparation the review and the submission of the CSR with Medical Writing.
- Ensure the finalization and archiving of the eTMF.
Qualifications
- Bachelors life science degree or Masters degree or equivalent
- Experience in pharmaceutical drug development (Ph2 Ph3)
- Experience in project management of national and international programs
- Relevant experience in RWE/HEOR NIS studies
- Experience and know-how in Oncology or in Rare Diseases or in Neurosciences
- Proven track record of delivery of projects to time budget and quality.
- Strong knowledge of Good Clinical Practice (GCP)
- Experience of managing and developing relationships with Service Providers
- English fluency
- Computer literacy
- Ability to travel as required with the needs of the role up to approximately 25% of the time.
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Nous nous engageons à créer un lieu de travail où chacun se sent écouté valorisé et soutenu où nous incarnons The Real Us*. La valeur que nous accordons aux différentes perspectives et expériences motive notre engagement en faveur de linclusion et de légalité des chances. Lorsque nous intégrons des modes de pensée diversifiés nous prenons des décisions plus réfléchies et découvrons des solutions plus innovantes. Ensemble nous nous efforçons de mieux comprendre les communautés que nous servons. Cela signifie que nous voulons également vous aider à donner le meilleur de vous-même lorsque vous postulez à un poste chez nous. Si vous avez besoin daménagements ou daide pendant le processus de candidature veuillez en informer léquipe de recrutement. Ces informations seront traitées avec soin et nauront aucune incidence sur le résultat de votre candidature. *Soyons nous-mêmeRequired Experience:
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About Company
Ipsen is a global biopharmaceutical company focused on innovation and specialty care to improve the lives of patients around the world.
