Senior Clinical Research Associate (Contract)

Atlas Search; Colorado; On-site; USD 85,000 - 110,000; Full time

Job summary

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

Qualifications

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

Responsibilities

• 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.

Skills

Monitoring experience

Oncology experience

Site management

Education

Bachelor's degree in life science

Job description

We are working with a fast growing organization who is seeking to bring on experienced Sr. Clinical Research Associates located in Colorado. The role requires limited to no travel and offers a tremendous opportunity to partner with a growing, high-quality and innovative team.

Responsibilities:

• Interact with personnel from study Sponsors, investigational sites, vendors, and functional groups to enable quality and on-time 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, Case Report Form completion guidelines, monitoring plans, informed consents, recruitment materials, and monitoring tools, as needed.
• Perform Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits in compliance with the approved protocol and monitoring plan.

Requirements:

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