Clinical Trials Operations Specialist
3 days ago
As a Clinical Trials Operations Specialist, you will play a pivotal role in the success of our research projects.
Key Responsibilities:- Manage study visit scheduling to ensure timely and efficient progress.
- Coordinate sample processing and shipping to maintain high-quality standards.
- Track finances and contracts to facilitate smooth study start-up activities.
- Support patient recruitment by collaborating with study coordinators.
- Assist with transitioning trial documentation to digital systems for enhanced efficiency.
- Coordinate research events, including conferences and workshops, to foster collaboration and knowledge sharing.
- Communicate effectively with colleagues and stakeholders to drive successful outcomes.
- Contribute to a dynamic team environment valuing excellence in research administration and project support.
Qualifications/Skills:
- Demonstrate strong project management and administrative skills within a clinical research setting.
- Show ability to work independently and as part of a collaborative team.
- Exhibit attention to detail, high computer literacy, and commitment to confidentiality and research standards.
We champion a workplace culture that values diversity and inclusivity. Our team members enjoy a sense of belonging, contributing to groundbreaking work, and experiencing a workplace where great things happen.
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