Senior Clinical Research Associate

Atlas Search; United States; Remote; USD 70,000 - 100,000; Full time

Job summary

A growing clinical research organization in the United States is seeking experienced Clinical Research Associates nationwide. This role offers remote work opportunities with limited travel and focuses on clinical trial execution. Candidates must hold a Bachelor's degree in a life science, possess 3-5 years of monitoring experience, and have knowledge of oncology radiopharmaceuticals. This is a chance to join an innovative team committed to quality research.

Qualifications

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

Responsibilities

• Interact with personnel from study Sponsors and sites for trial execution.
• Identify potential sites for clinical trials.
• Perform protocol/site feasibility and Pre-Study Visits.
• Participate in Investigator Meetings and training sessions.
• Provide feedback to study manuals and monitoring tools.
• Perform Site Initiation, Interim, and Close-Out Visits.

Skills

Clinical trial execution

Site feasibility assessment

Oncology Radiopharmaceutical knowledge

Monitoring experience

Education

Bachelor’s degree in a life science or related field

Job description

We are working with a fast growing organization who is seeking to bring on experienced 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 Radiopharmaceutical experience required