Senior Clinical Trial Manager ensuring successful clinical study delivery and effective management of clinical budgets at ICON. Overseeing study integrity and fostering relationships with stakeholders.
Responsibilities
Oversee the clinical portion of the budget to ensure efficient resource allocation.
Develop monitoring plans and tools, ensuring effective study oversight.
Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
Drive enrollment and lead study start-up activities, adhering to timelines.
Review trip reports and implement corrective and preventative action plans when necessary.
Foster productive relationships with Sponsors, vendors, and cross-functional teams.
Requirements
A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
Bachelor's degree in health, life sciences, or other relevant fields of study.
At least 10+ years of relevant experience in clinical trial management.
Preferred: 2+ years of monitoring experience.
Experience in managing complex or global trials is advantageous.
Preferred: Experience in managing all trial components from start-up to database lock.
Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
Fluency in English (reading, writing, speaking).
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 specialised 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, subsidised travel passes, health assessments, among others.
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