Senior CRA – Oncology, Low Travel, Colorado

Atlas Search; Colorado; Vor Ort; USD 85.000 - 110.000; Vollzeit

Zusammenfassung

Atlas Search in Colorado is seeking a Sr. Clinical Research Associate to oversee monitoring of oncology trials with limited travel.

You will interact with sponsors and sites to ensure quality and on-time execution, identify eligible sites, and conduct feasibility and pre-study visits. Responsibilities include supporting investigator meetings and trainings, updating manuals and monitoring plans, and performing initiation, interim, and close-out visits per protocol to ensure compliant study

Qualifikationen

• Bachelor’s degree in a life science or related field of study.
• Minimum of 3 – 5+ years monitoring experience.
• Oncology monitoring experience required.

Aufgaben

• Interact with Sponsors, investigational sites, vendors and functional groups to ensure quality and timely execution of clinical trials.
• Identify potential sites for participation in clinical trials.
• Perform protocol/site feasibility and Pre-Study Visits to recommend qualified sites.
• Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites with study-related questions as needed.
• Provide feedback to study manuals, CRF completion guidelines, monitoring plans, informed consents, recruitment materials, and monitoring tools.
• Perform Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits in accordance with the protocol and monitoring plan.

Kenntnisse

Monitoring experience

Oncology experience

Site management

Ausbildung

Bachelor's degree in life science

Jobbeschreibung

Atlas Search in Colorado is seeking a Sr. Clinical Research Associate to oversee monitoring of oncology trials with limited travel.

You will interact with sponsors and sites to ensure quality and on-time execution, identify eligible sites, and conduct feasibility and pre-study visits. Responsibilities include supporting investigator meetings and trainings, updating manuals and monitoring plans, and performing initiation, interim, and close-out visits per protocol to ensure compliant study