Clinical Trial Manager

Imperative Care•Campbell, CA

9d•$136,000 - $152,000•Hybrid

About The Position

Imperative Care is seeking a seasoned Clinical Trials Manager to join their team. This role will be responsible for carrying out all tactical aspects of assigned clinical trials from study initiation to monitoring adherence to design protocols, identifying and resolving issues at study sites and with CROs, and facilitating effective clinical programs. This job will contribute to and support the company's research and development efforts to create high-value medical devices to address unmet clinical needs.

Requirements

Bachelor’s degree in related field and a minimum of 5 years of clinical research management experience, preferably in medical device industry; or a combination of education/training and experience.
Demonstrated experience and success in IDE studies and neurovascular therapeutic area.
Extensive knowledge of FDA requirements, GCPs, other regulatory guidelines at a hospital, and health care environments.
Ability to collaborate with and coordinate the work of clinical trial teams.
Excellent written and verbal communication skills required.
Demonstrated experience interacting with physicians, clinicians, and patients.
Ability to be very flexible, adaptable, and work under pressure.
Self-motivated and self-directed; detailed approach to work assignments; able to multitask and work at a fast-paced environment while able to adapt to frequent shifts in priorities.
Excellent interpersonal and negotiating skills; able to maintain good working relationships while dealing appropriately with sensitive and confidential matters and with a wide variety of personal and telephone contacts.
Must be willing to travel 20 - 30%.

Responsibilities

Lead day-to-day execution of clinical studies from site initiation through close-out, ensuring timelines, enrollment goals, and study quality are consistently achieved.
Serve as the primary partner to investigational sites, CROs, CRAs, and sponsor stakeholders to drive strong site engagement, issue resolution, and successful study delivery.
Oversee and support clinical data quality, query management, protocol compliance, and study documentation to ensure inspection readiness and regulatory excellence.
Monitor site performance, enrollment progress, and operational metrics; proactively identify risks and implement solutions to maintain study momentum.
Contribute operational expertise to the development of study protocols, clinical study documents, and cross-functional clinical initiatives that support innovative neurovascular medical device programs.