Clinical Trial Manager - Spain - Up to €100,000

Here at Upsilon Global we have a fantastic new opportunity for an experienced CTM to join one of our long term mid-sized partners who specialise in a range of therapeutic areas; predominantly drug and device trials.

Able to offer thorough and rigorous training, this is a unique chance to join a company who a truly passionate about what they do, and the efforts you make really matter. 

Responsibilities

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables
• Maintain in depth knowledge of protocol, therapeutic area, and indication
• Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
• Develop operational project plans
• Manage risk assessment and execution
• Responsible for management of study vendor
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Qualifications

• Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred;
• Experience in Phases 1-4; Phases 2-3 preferred;
• Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred;
• 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role;
• Management of overall project timeline;
• Bid defense experience preferred; and
• Strong leadership skills.