
Senior International Site Activation Specialist
Há 13 horas
We are seeking an accomplished professional to spearhead site activation, maintenance and regulatory activities for selected studies or multi-protocol programs. This individual will oversee the execution of feasibility, site identification, site activation and/or maintenance for assigned projects, developing and implementing management plans in accordance with project timelines.
Main Responsibilities:
- Oversee the execution of site activation, including pre-award/bid defense activities, within agreed project timelines.
- Develop, implement and maintain management plans according to scope of work and project plan, resolving project-related issues as needed.
- Ensure collaboration across feasibility, site identification, regulatory and site activation teams, including communication with regions and countries, to successfully deliver agreed project scope in compliance with RSU Management Plan.
- Create and review technical and administrative documentation to support business development and enable study initiation and maintenance.
- Provide specialist functional and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, while enabling compliance with functional/regulatory requirements.
Requirements:
- Bachelor's degree in a life science-related discipline.
- 7 years' relevant experience in a scientific or clinical environment, including demonstrable experience in an international role.
- Thorough understanding of regulated clinical trial environment and knowledge of drug development process.
- Advanced level of English.
Note: Experience with site relationships, site identification, clinical protocols, and leadership skills are highly desirable.
This is an opportunity to take your career to the next level and make a meaningful contribution to the success of our organization.
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