Senior Clinical Trial Manager
Detalhes do emprego
You will need to login before you can apply for a job. Sector: Research and Development, Science and Pharmaceutical Role: Senior Executive Contract Type: Permanent Hours: Full Time Senior Clinical Trial Manager - Mexico & Brazil - Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. The Role: We are currently seeking a Senior Clinical Trial Manager in the Biotech Division, aligned with therapeutic areas such as General Medicine (NASH), Rare Diseases, or Oncology , to join our dynamic and diverse team. As a Clinical Trial Manager at ICON, you will lead global clinical trials, interpret complex medical data, and contribute to the development of groundbreaking treatments and therapies. What you will be doing:
- Leading and managing all aspects of global clinical trial activities, from planning and execution to close-out.
- Collaborating with cross-functional teams to develop trial protocols, study plans, and strategies.
- Monitoring trial progress to ensure adherence to timelines, budgets, and quality standards.
- Managing relationships with third-party vendors, including selection, oversight, and performance evaluation.
- Providing leadership, guidance, and mentorship to project teams, fostering effective communication and problem-solving.
- Participating in sponsor meetings, investigator meetings, and bid defense meetings as a key contributor.
- Minimum 4.5 years of experience for consideration at the Senior CTM level.
- Global trial management experience is required, with a strong focus on the US and Canada.
- Experience working with the Advarra Ethics Committee is highly desirable.
- At least 3+ years of monitoring experience is strongly preferred.
- Prior experience managing all trial components (from start-up to database lock) is preferred.
- Bachelor's degree in a health, life sciences, or other relevant field, required.
- Demonstrated ability to manage complex or global clinical trials.
- Experience in coaching and mentoring other CTMs, leading teams, and contributing to departmental initiatives.
- Strong proficiency in English (spoken and written) is required.
- For candidates based in Brazil, comfort with Spanish is an advantage.
- 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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.
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