Senior Clinical Trial Manager, Oncology - Biotech

SEC Recruitment
£124933.50 - £141591.30 per annum + Annual bonus
Closing date
6 Oct 2020

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Clinical Research, Clinical Project Manager, Clinical Study Manager
Full Time
Contract Type
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Senior Clinical Trial Manager - Permanent
Lausanne area with WFH flexibility

An exciting opportunity with a growing Biotechnology company in the Lausanne region is currently seeking a Senior Clinical Trial Manager on a permanent basis, a role initially aligned to early development but which will work predominantly within oncology to provide cross-functional leadership and have the opportunity to contribute to activities more associated with clinical science (i.e. protocol design/development).

Key Responsibilities:

- Accountable for the leadership and oversight of multiple (likely 2) global clinical trials within oncology and anti-infectives across all stages of the drug development process (Phase I-III).
- Ensure completion of studies undertaken in accordance with timelines, study plans, quality, resources and budget.
- Ultimate oversight and participate in the selection of external vendors (CRO's, independent consultants and other vendors) to ensure delivery against agreed scope of work.
- Oversight of the global study management team and all functions involved in study (clinical site management, biometrics, regulatory, central labs etc).
- Responsible for study finances across region/countries assigned as part of company-sponsored post-marketing studies, in addition to grants for investigator initiated studies.
- Support the local organisation in achieving and delivering the organisation's local and regional medical strategy.
- Ensure that Clinical Trial Management System is updated as necessary.

The Ideal Candidate Will Have:

- Must hold a life science or medical-related degree or equivalent qualification.
- Previous clinical trial management experience in a CRO, Biotech or Pharmaceutical Company within the Oncology TA, though other complex areas (rare diseases, neuroscience, infectious diseases) would be sought after.
- Experience in clinical trial planning and conduct.
- Thorough knowledge of ICH-GCP and applicable local/regional regulations.
- Experience of leading global Phase II-III clinical trials, with experience in managing trials with an adaptive design a definite advantage.

Overall this vacancy represents a fantastic opportunity to join a Biotech with an exciting pipeline on a permanent basis, with the perfect platform to develop and enhance your career in the long term in an innovative and forward-thinking environment. There is also a highly competitive remunerations package available for the right candidate.

If you would like to apply for this position, please forward your CV to or call Sam Doherty on +44 (0) 207 255 6665 for more information.

It’s easy to say, ‘we’re different’ as a recruitment business, which is why at SEC we like to show our candidates and clients that we are through our actions and our delivery. We are a life sciences and IT specialist recruitment agency that lives by four core values of trust, honesty, integrity and commitment. To us these are more than just words on a website. These are ways in which we want you to feel every time you talk to us.

Our aim is to be the European life sciences partner of first choice to everybody who works with us. We speak over 20 different languages collectively and can support you with what you need.

So, talk to us. Call us, browse our jobs, see how we are helping change both people and employers’ lives.

Contact Us
  • 3rd Floor,
  • 13-15 Moorgate
  • EC2R 6AD
  • GB
  • 00 44 (0) 207 255 6600
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