Senior Clinical Project Manager - Belgium

i-Pharm Consulting are partnering with a Mid-size CRO Company who are seeking an experienced Senior Clinical Project Manager in Belgium

THE COMPANY

i-Pharm has been a dedicated recruiter for this client for a number of years and have had great feedback on the company's career progression, culture and job satisfaction from candidates placed in both permanent and contract positions.

TITLE:

Clinical Project Manager

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-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; required for home-based
• Management of overall project timeline
• Bid defense experience, preferred
• Strong leadership skills

LOCATION:

• Belgium
• Home based or Office based

About i-Pharm Consulting

i-Pharm Consulting is a global specialist recruitment company servicing the pharmaceutical industry. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com