Responsibilities:
- Lead and develop a team of remote pre-screening clinical research coordinators, focusing on performance, accountability, and quality management.
- Assess and improve site-level patient pre-screening workflows to ensure efficient and reliable patient identification.
- Own operational management of pre-screening activities, including rigorous tracking, analysis, and reporting of key performance metrics.
- Serve as a bridge between leadership and frontline teams, translating strategic priorities into execution and operational insights into improvements.
Qualifications:
- 5+ years of experience in clinical research, healthcare operations, or related patient-facing roles with demonstrated leadership experience.
- Deep clinical foundation, preferably in clinical research operations, site workflows, and oncology, with knowledge of trial protocols and eligibility.
- Proven ability to manage and optimize workflows, analyze performance metrics, and drive process improvements in a dynamic environment.
Offerings:
- Comprehensive Total Rewards package including competitive health, dental, and vision insurance, and mental health support for you and your family.
- Unlimited paid time off (PTO) and 16 weeks of paid parental leave to support work-life balance and family needs.
- Flexible work options with remote and hybrid arrangements, plus company-paid life insurance, disability coverage, and a 401(k) plan with company match.
Paradigm
Paradigm is a clinical research company rebuilding the ecosystem to enable equitable trial access for all patients and improve efficiency for healthcare providers. It is a venture-backed team from diverse disciplines committed to bringing life-saving therapies to patients faster.