Senior Regional Study Manager
il y a 1 semaine
- Oversee the clinical portion of the budget to ensure efficient resource allocation.
- Develop monitoring plans and tools for 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 as necessary.
- Foster productive relationships with Sponsors, vendors, and cross-functional teams.
- A minimum of 6 years of experience in Clinical Trial Management at a CRO or Pharmaceutical Organization.
- Must have experience managing Infectious Disease and Vaccine studies.
- Bachelor's degree in health, life sciences, or relevant fields.
- At least 10+ years of relevant experience in clinical research.
- Preferred: 2+ years of monitoring experience.
- Experience in managing complex or global trials is advantageous.
- Preferred: Experience managing all trial components from start-up to database lock.
- Preferred: Experience in coaching/mentoring other CTMs and leading a team.
- Fluency in English (reading, writing, speaking).
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings for future savings.
- Global Employee Assistance Programme with 24-hour access to support.
- Life assurance.
- Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships.
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