Key skills
Mentoring
About this role
Role Overview
- 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.