Global Clinical Trial Manager

An opportunity has opened for a Global Clinical Trial Manager to join a cutting-edge, medium sized Pharmaceutical company based in Zurich & Geneva to oversee their rare disease's portfolio. You'll be joining the company at an exciting time of growth with plans to grow their Clinical Operations team by a further 40% by the end of the year due to their strong financial backing. For this role, you'll have the opportunity to step into Senior CTM level quickly within the next 18 months as the team continues to grow - perfect for an individual who is looking for fast career development within an established Pharmaceutical company.

You'll be managing two Phase IIb global studies so having prior global experience is essential so you can hit the ground running straight away. The position can be office based in either of their two office locations in Zurich or Geneva with some home working flexibility. A highly attractive financial package is also on offer + 10% bonus + much more.

Responsibilities:

• Planning and feasibility assessments of clinical trials
• Operational excellence in GCP/ICH compliant execution of global clinical trials (management of budget and timelines as well as delivery of quality)
• External service provider / vendor management for clinical trial execution
• Leadership of Clinical Study Teams. Member of cross functional teams
• Support of Clinical Operations tools & departmental development

Tasks:

• Contributes to development and operational design, planning of budget and timelines, feasibility assessments and initiation of clinical trial protocols and programs
• Leads internal cross functional Clinical Study Teams responsible for conducting global clinical trials to ensure project deliverables are executed on time and within budget with full oversight
• Manages external service providers including CRO(s), vendors and subcontractors
• Efficient & effective communication, exchange of information across projects & reporting lines
• Ensures clinical trials are conducted according to GCP and all applicable regulations.
• Contribution to essential study documents, coordination of reviews, manages audits & inspections

Minimum Requirements

Education

• Relevant University Degree in natural or medical sciences

Experience

• 3+years monitoring and successful management experience in global clinical trials in pharmaceutical industries or CROs
• Experienced team player having been a member of cross-functional and multi-cultural teams
• Demonstrated success in coordinating external resources for clinical development and in working with pharmaceutical partners
• Experience and understanding of the drug development process and clinical trial execution
• Understanding of clinical aspects of therapeutic area along with willingness to develop in-depth expertise
• Excellent user of Office Programs (Word, Excel, PowerPoint, MS Project)

Languages

• Fluency in English

Preferred Requirements

• Experience in leadership of cross-functional teams
• Additional language e.g. French or German would be appreciated

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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