https://www.fradeo.com/fr/candidats/offres-emploi-franco-allemandes/clinical-senior-project-manager-m-w-d
Clinical Senior Project Manager (m/w/d)
- Munich
- 4 janvier 2022
- Réf. FRDJOB2021102913163705
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nabios - Banook group
The Banook Group is one of the few international providers capable of supplying cardiac safety, central imaging and endpoint adjudication services to pharmaceutical groups, biotech companies, medical device manufacturers, CROs and nonprofit organizations.
Its mission is to help its clients develop the healthcare of tomorrow, using high quality, reliable and innovative solutions in all phases of clinical trials and ultimately to bring new solutions to market for the benefit of patients.
Its medical and regulatory expertise, quality-driven approach and team availability, make the Banook group a key player in clinical trials services.
Founded in 1999, the Banook Group operates on an international scale, maintaining offices at its headquarters in Nancy, (France), and in Montreal (Quebec, Canada)
Its mission is to help its clients develop the healthcare of tomorrow, using high quality, reliable and innovative solutions in all phases of clinical trials and ultimately to bring new solutions to market for the benefit of patients.
Its medical and regulatory expertise, quality-driven approach and team availability, make the Banook group a key player in clinical trials services.
Founded in 1999, the Banook Group operates on an international scale, maintaining offices at its headquarters in Nancy, (France), and in Montreal (Quebec, Canada)
nabios was founded in 1998 and has developed a strong expertise in cardiac safety assessments in clinical trials of drugs intended for human health. It supports pharmaceutical companies, Contract Research Organizations (CROs) and Clinical Pharmacology Units (CPUs), primarily in the conduct of Phase 1 clinical trials. nabios has a number of preferred provider partnerships, mostly based in Germany, including two of the top 20 big pharma companies and several Phase 1 units.
While becoming a part of the Banook Group, nabios will retain its current name built on its strong reputation. The Banook Group will strengthen its teams in Munich to enhance their presence in Central and Eastern Europe.
What will you be doing?
- Coordinate clinical trials from startup to close out,
- Act as primary point of contact for client/sponsor,
- Manage and coordinate efforts of cross-functional project teams (data management, clinical trial coordinators, quality) to support milestone achievement and to manage study issues and obstacles,
- Ensure all project deliverables meet customers’ expectations as well as company’s standards,
- Prepare and present project information at internal and external meetings,
- Ensure development of study specifications and documentation,
- Monitor and report on the progress of all project activity within the project including significant milestones and any conditions which would affect project cost or schedule,
- Assist in the development of standard operating procedures and other documented practices,
- Manage and coordinate a team of Project Managers
Who are you?
- Are you self-motivated and looking for a job where you can be part of a collaborative team?
- Are you a natural leader with a passion for clinical development and an appetite for project management?
- Can you demonstrate spirit of collaboration in particular with staff in other teams to coordinate relevant activities?
- Can you provide excellent leadership to not only your project teams, but also to clients?
- Are you organized, but adaptable to unexpected changes?
- Do you have effective organizational and time management skills?
- Can you easily take a step back from the day to day without losing the sight of your daily commitments?
- Can you demonstrate analysis and synthesis skills?
- Are you recognized for your leadership qualities and management skills?
Most of all, do you want to get involved in a place you love working. If so, come join us rapidly!
What you need to qualify?
- Master’s degree in life sciences or related field and 5 years’ clinical research experience including 2 years’ project management experience in clinical operations,
- Exposure to cardiac safety evaluation or/and imaging techniques,
- Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials,
- International CRO experience, ability to work across different therapeutic areas,
- Demonstrate experience managing multiple projects in a highly virtualized team environment,
- Read, write and speak fluent German and English,
- Basic knowledge in French (B1 Level) nice to have but not mandatory.
