Senior Clinical Research Associate - Oncology (Remote - Minnesota)

AbbVie; Minneapolis (MN); Remote; USD 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in Minneapolis is looking for a Clinical Research Associate to ensure effective execution of studies. The role requires 3+ years of monitoring experience and a Bachelor’s degree. You will conduct site evaluations and manage compliance while working in a dynamic environment. This position offers a competitive salary and comprehensive benefits package.

Benefits

Competitive salary

Comprehensive benefits package

Career advancement opportunities

Dynamic work environment

Qualifications

• Minimum of 3 years of site monitoring experience.
• Bachelor’s degree required.

Responsibilities

• Ensure successful protocol level execution of deliverables.
• Conduct monitoring visits and site evaluations.
• Identify solutions for site issues affecting timelines.
• Maintain compliance with regulations and quality standards.
• Prepare for audits and inspections.

Skills

Analytical skills

Critical thinking

Interpersonal skills

Communication skills

Planning and organizing

Education

Bachelor's degree

Job description

Overview

Employer Industry: Pharmaceutical Research & Development

Why consider this job opportunity

• Competitive salary range with eligibility for short-term and long-term incentive programs
• Comprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)
• Opportunity for career advancement through mentorship and coaching of CRAs
• Work in a dynamic environment with a focus on innovative clinical research
• Engage in meaningful work that contributes to the development of life-changing medicines

What to Expect (Job Responsibilities)

• Ensure successful protocol level execution of deliverables involving start-up, execution, and close-out of studies
• Conduct monitoring visits, site evaluations, site selection, activation, and manage close-out and visit reports
• Identify and develop solutions for site issues that may affect study timelines
• Maintain clinical trial management systems and ensure compliance with regulations and quality standards
• Prepare for audits and inspections, providing input into corrective action plans

What is Required (Qualifications)

• Bachelor’s degree
• Minimum of 3 years of site monitoring experience
• Strong analytical and critical thinking skills
• Excellent interpersonal and communication skills
• Proven ability to plan and organize effectively in a dynamic environment

How to Stand Out (Preferred Qualifications)

• Health-related degree (e.g., Medical, Scientific, Nursing, Pharmacy)
• Demonstrated proactive team player with resourcefulness and creativity
• Experience in managing multiple competing projects and deadlines

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