Senior Clinical Research Associate

Atlas Search; Colorado; Remote; USD 90,000 - 120,000; Full time

Job summary

Atlas Search is seeking a Senior Clinical Research Associate to join our expanding team. This nationwide role focuses on monitoring clinical trials with limited travel and partners closely with sponsors, sites and functional groups to ensure quality and on-time execution.

As a CRA, you will identify potential sites, perform feasibility assessments, conduct site initiation and interim visits, and help prepare manuals and monitoring tools.

Qualifications

• Bachelor’s degree in a life science or related field.
• Minimum of 3–5+ years monitoring experience.
• Oncology/CNS/Pain monitoring experience preferred.

Responsibilities

• Interact with Sponsors, sites, vendors, and teams to ensure quality and on-time trial execution.
• Identify potential sites for participation in clinical trials.
• Perform protocol/site feasibility and Pre-Study Visits to qualify sites.
• Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites with study-related questions.

Skills

Monitoring experience

Clinical trial coordination

Site identification

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 nationwide. 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, CNS or Pain Management monitoring experience preferred