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Medical Research Project Manager
1 month ago
At Intuitive Surgical, we strive to push the boundaries of minimally invasive care. With a strong commitment to innovation and patient safety, we aim to make a lasting impact on the world of healthcare.
We are united by our mission: to advance the capabilities of physicians and improve patient outcomes through cutting-edge technology. Our team is dedicated to fostering an inclusive and diverse environment, where great ideas can thrive and talented individuals can grow.
We lead with inclusion, empowering our team members to excel in their roles and contribute to our collective success. With a focus on long-term growth and development, we invest in our employees' futures, ensuring they have the skills and expertise needed to drive our mission forward.
About This RoleThis Clinical Project Manager position plays a critical role in our European operations, overseeing the initiation, progression, and conduct of clinical studies sponsored by Intuitive Surgical. The successful candidate will serve as the primary contact for all parties involved in these projects, both internal and external.
This role requires excellent project management skills, a deep understanding of applicable regulations, and the ability to ensure seamless collaboration between various stakeholders. If you're passionate about driving medical research forward and committed to upholding the highest standards of quality and compliance, we want to hear from you.
The ideal candidate will possess a graduate qualification in Life Sciences, Medicine, or Medical Sciences, with a minimum of three years' experience in clinical affairs/research functions within the medical device industry. Strong numerical and literary analytic skills, combined with excellent communication and interpersonal abilities, are essential for this role.
Main Responsibilities- Manage and execute clinical research activities, including protocol and CRF development for pre- and post-market trials.
- Ensure adherence to safety reporting requirements per local, national, and European regulations.
- Supervise study documentation, including CRA and clinical study coordinator activities.
- Plan and manage project timelines, budgets, and resources to meet project objectives.
- Develop risk assessments and contingency plans to mitigate potential issues.
- Prepare project status updates and presentations for internal stakeholders.
As a valued member of our team, you'll enjoy a competitive salary package, including an estimated annual salary of $95,000 - $115,000, depending on experience. You'll also benefit from a comprehensive benefits program, including health insurance, retirement plans, and paid time off. In addition, you'll have access to ongoing training and professional development opportunities, enabling you to grow your skills and expertise.
We value diversity, equity, and inclusion and are committed to creating a work environment that supports the well-being of all our employees. If you're passionate about medical research and committed to excellence, we encourage you to apply for this exciting opportunity.
