Clinical Project Manager - officebased

Upsilon Global are working with a global CRO who are headquartered in the US and have 3,000 + employees in over 30 countries globally. As a full service CRO they work in various therapeutic areas that include oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective in all Phases I-IV working in partnership with pharmaceutical and biotechs.

The CRO has over 25 years of experience working in the clinical research field and pride themselves to have been awarded 1st Place in the CRO quality award and CRO awards in leadership.

The CRO has an office in Belgium and is seeking Clinical Project Managers to join their team in an office-based position with the opportunity to become a flexi position.

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:

• Minimum Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
• Experience in Phases 1-4; Phases 2-3 preferred
• 5+ years as a project/clinical trial manager within a CRO
• Management of overall project timeline
• Bid defense experience, preferred
• Strong leadership skills