Senior Clinical Trial Activation Manager
hace 5 horas
About ICON
ICON is a world-leading healthcare intelligence and clinical research organization dedicated to fostering innovation and excellence in the industry. Our mission is to shape the future of clinical development, and we invite talented professionals to join our diverse and dynamic team.
About the Role
We are currently seeking a highly skilled Sr. Clinical Trial Activation Manager to advance clinical trial start-up activities by understanding client objectives and assisting in the development of plans for country and site distribution. As a key member of our team, you will oversee day-to-day delivery of all aspects of site activation in assigned projects, ensuring adherence to sponsor timelines, expectations, and compliance with ICON/client KPIs, SOPs, and regulatory standards.
Key Responsibilities:
- Lead clinical trial start-up activities, understanding client objectives and assisting in the development of plans for country and site distribution.
- Oversee day-to-day delivery of all aspects of site activation in assigned projects, ensuring adherence to sponsor timelines, expectations, and compliance with ICON/client KPIs, SOPs, and regulatory standards.
- Ensure that each project has a comprehensive site activation plan, conducting studies effectively in accordance with the plan.
- Lead sponsor initiatives such as kick-off meetings, bid defenses, project updates, status calls, and other key communications.
- Utilize project management skills to optimize performance and collaboration, ensuring successful study outcomes.
Your Profile:
- Bachelor's Degree, preferably in life sciences.
- Minimum of 5 years of experience in a Clinical Research environment, focusing on Start-Up experience.
- Strong project management skills, with a deep understanding of regulatory and submission processes in various countries.
- Excellent written and verbal communication abilities.
- Proven ability to work efficiently to tight deadlines and manage multiple priorities.
About You:
As a seasoned professional in the field of clinical research, you possess excellent project management skills and a deep understanding of regulatory processes. Your strong communication abilities and ability to work under pressure make you an ideal candidate for this role. If you are a motivated individual who is passionate about advancing clinical trials, we encourage you to apply for this exciting opportunity.
Benefits:
- Our competitive salary package includes an estimated $**124,000** per annum.
- A range of health insurance offerings to suit your needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Diversity and Inclusion:
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative, which helps us better serve our people, patients, customers, and communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organization. We're dedicated to providing an inclusive and accessible environment for all candidates.
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