Senior Clinical Research Associate

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

Job summary

Atlas Search is seeking a Senior Clinical Research Associate to support clinical trials nationwide with limited travel and close collaboration with sponsors, sites and cross-functional teams.

The ideal candidate has 3–5+ years of monitoring experience, a life-science degree, and familiarity with oncology, CNS, or pain management trials.

Qualifications

• Bachelor's degree in a life science or related field.
• 3–5+ years monitoring experience.
• Oncology, CNS or Pain Management monitoring experience preferred.

Responsibilities

• Interact with Sponsors, 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, and assist sites with study-related questions.
• 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 compliance with the protocol and monitoring plan.

Skills

Clinical trial monitoring

Site feasibility

Study coordination

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