ICON plc
ICON plc is a leading global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, medical device, and government industries. Offering a comprehensive range of services including clinical trial management, regulatory affairs, and market access solutions, ICON leverages advanced technologies and innovative methodologies to improve the efficiency and effectiveness of drug development processes. With a strong commitment to patient-centered approaches and a focus on therapeutic areas like oncology and rare diseases, ICON is dedicated to transforming clinical research to deliver better healthcare outcomes.
Medical Device • Therapeutics • Government and Public Health Solutions • Clinical Research Services • Commercialisation and Outcomes
Global Clinical Project Manager
March 26
ICON plc
ICON plc is a leading global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, medical device, and government industries. Offering a comprehensive range of services including clinical trial management, regulatory affairs, and market access solutions, ICON leverages advanced technologies and innovative methodologies to improve the efficiency and effectiveness of drug development processes. With a strong commitment to patient-centered approaches and a focus on therapeutic areas like oncology and rare diseases, ICON is dedicated to transforming clinical research to deliver better healthcare outcomes.
Medical Device • Therapeutics • Government and Public Health Solutions • Clinical Research Services • Commercialisation and Outcomes
📋 Description
• Joining a well-established yet expanding team fully outsourced to one of our global pharmaceutical clients • The Clinical Trial Manager ensures successful execution of phase 1-4 clinical trials globally • Serving as the leader for the Study Management Team, managing project milestones and communication between departments • Ensures accurate budget management and guarantees third-party vendors are working to defined plans • Driving activity to ensure enrolment commitments are met and resolving problems proactively • Delivering training to the study team on a trial-specific basis and liaising with Quality Management
🎯 Requirements
• Expert study manager with a proven record of successful execution of clinical trials globally • Experience in the set-up and management of third-party vendors, as well as global study start-up • Familiarity with Phase I-IV studies highly advantageous • Demonstrable knowledge of effective project planning and strong financial acumen • Flexibility to manage a virtual team • Previous experience working with multiple therapeutic areas, including oncology, cardiology/metabolism, infectious disease, immunology and/or vaccines preferred • 3-5 years clinical trial management/trial oversight experience in the pharmaceutical industry or CRO • Proven track record in successfully managing various aspects of trials from Start-Up to Database Lock and Trial Closure (End to End) • Experience coordinating global or regional teams in a virtual environment for a minimum of 3 years • Willing to travel up to 20%
🏖️ Benefits
• Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
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