At a Glance
- Tasks: Lead global clinical projects and ensure successful delivery of new medicines.
- Company: Join ICON, a leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, professional development, and a values-driven culture.
- Other info: Dynamic work environment with opportunities for growth and collaboration.
- Why this job: Make a real difference in patients' lives by managing innovative clinical studies.
- Qualifications: Bachelor's in Science, 10 years clinical experience, and strong leadership skills.
The predicted salary is between 51750 - 63250 £ per year.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.
You will be the primary Study Management point-of-contact in the event of an audit or inspection. Provide regular feedback on individual performance to the study team members and their line managers to support their professional development; may mentor less experienced colleagues.
Your Profile
- Bachelor’s degree in Science related field is a must, with significant experience in project management and team leadership.
- 10 years of relevant clinical experience in the pharmaceutical industry, including 5 years’ Global clinical project management experience, or equivalent Early Phase Hematology experience.
- Proven track record of successfully managing projects from inception to completion, with a focus on delivering results within scope, time, and budget constraints.
- Strong leadership and organizational skills, with the ability to effectively manage project teams and prioritize tasks.
- Experience across all Phases and lifecycle of the clinical studies.
- Experience managing multiple amendments during early phase studies.
- Excellent communication and interpersonal skills, with the ability to build relationships and manage stakeholder expectations.
- Proficiency in project management tools and methodologies, with certifications such as PMP or PRINCE2 being advantageous.
- Detail-oriented, proactive, and adaptable, with a commitment to achieving project goals and driving continuous improvement.
- Extensive knowledge of ICH-GCP, clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development.
- Demonstrated solid project management skills and knowledge of relevant tools.
- Strong, demonstrated abilities/skills in team leadership.
- Strong abilities in establishing and maintaining effective working relationships with internal and external co-workers and stakeholders, along with strong conflict management skills.
- Strong strategic and critical thinking abilities.
- Strong organizational and problem-solving skills.
Global Clinical Project Manager Reading employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
