Description
As a Senior Project Manager at ICON, you will be responsible for leading full-service clinical research projects from study start-up through closeout, ensuring successful execution and delivery of project objectives.
Key responsibilities include:
- Developing and executing project plans, focusing on achieving project goals and objectives across full-service clinical trials.
- Providing end-to-end project leadership across study start-up, conduct, and closeout, coordinating cross-functional clinical research activities and deliverables.
- Leading cross-functional teams to ensure the successful implementation of project activities and alignment against project timelines, objectives, and commitments.
- Collaborating with stakeholders to identify project requirements, define project scope, and maintain alignment throughout the project lifecycle.
- Leading complex oncology studies, with the ability to apply relevant oncology and radiopharmaceutical clinical research experience to project execution.
- Mentoring and guiding team members, fostering a culture of excellence and continuous improvement.
- Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner.
- Staying abreast of industry trends and emerging technologies to integrate best practices into project management strategies.
- Contributing to organizational growth through effective project leadership and strategic planning.
You will have significant experience serving as the Project Lead/Project Manager for full-service clinical trials, with demonstrated ability to lead cross-functional teams and maintain oversight across the full study lifecycle.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Extensive clinical research project management experience within the pharmaceutical, biotechnology, or CRO industry, including direct experience leading full-service clinical trials.
- Demonstrated experience as the overall Project Lead with responsibility for coordinating multiple functional areas and driving successful delivery of studies from start-up through closeout.
- Strong oncology clinical trial experience.
- Experience with radiopharmaceutical/radioligand clinical trials is highly desired.
- Strong proficiency in project management tools and methodologies, with excellent attention to detail.
- Excellent analytical and problem-solving skills, with the ability to develop effective project strategies.
- Demonstrated leadership skills, with experience managing and mentoring cross-functional teams effectively.
- Exceptional communication skills, with the ability to convey technical concepts to diverse audiences.
- Detail-oriented, with strong organizational skills to manage multiple priorities and deadlines in a dynamic environment.
- Willingness to travel as required (approximately 25%).
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways