Clinical Research Scientist/Coordinator
We are seeking an experienced Clinical Research Scientist/Coordinator to lead the global start-up of clinical trials from protocol finalization through site activation. Reporting to the Clinical Development Team, you will create and execute study start-up plans, manage country submission packages, and driving on-time enrollment.
In this role, you will:
- Develop operational plans aligning study start-up activities with recruitment goals
- Configure systems and track the progress of documents, tasks, timelines, and milestones
- Assemble and ensure readiness of regulatory and ethics submission packages
- Provide oversight and risk management of study start-up processes across countries
- Lead cross-functional teams through study and site activation globally
- Ensure adherence to GCP, ICH guidelines, SOPs, and regulations
- Drive continuous improvement of start-up timelines and quality
Requirements
To excel in this role, you need:
- Degree in life science, healthcare, or a related field
- Experience successfully managing global clinical trial start-up
- Ability to influence and lead matrixed teams in complex environments
- Excellent project management, problem-solving, and negotiation skills
- Strong communication and partnership abilities
- Knowledge of clinical research processes, systems, and guidelines
We offer a collaborative environment, opportunities for growth, and competitive compensation. Come drive success and bring new treatments to patients faster as part of our clinical development team. Contact us today!