Senior Clinical Research Associate

Why This Role Matters
Clinical Research Associates (CRAs) play a vital role in ensuring that clinical trials are conducted ethically, safely, and in compliance with regulatory standards. Senior CRAs are particularly important because they oversee trial performance, maintain data integrity, and support investigative sites to ensure successful execution of research studies. Their work contributes directly to the development of innovative medicines that improve patient outcomes and advance medical science.

Job Description
The Senior Clinical Research Associate position with AbbVie is a research-focused role responsible for supporting clinical trial execution and ensuring high standards of data quality, regulatory compliance, and patient safety. This role partners closely with study teams, investigators, and clinical site staff to ensure proper conduct of clinical trials. The Senior CRA acts as a key liaison between the sponsor and investigative sites while monitoring clinical research activities and ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The position is based in Colorado and requires candidates to reside in the state and travel to clinical sites as required. The role focuses particularly on oncology clinical trials and involves collaboration with cross-functional research and development teams.

Key Features of the Role:
Remote-based research role with travel to clinical trial sites
Opportunity to work on oncology clinical trials within a global pharmaceutical organization
Direct collaboration with investigators, site staff, and clinical study teams
Leadership responsibilities including mentoring junior CRAs
Focus on maintaining data integrity, regulatory compliance, and patient safety

Responsibilities
Serve as the primary sponsor contact for investigative clinical trial sites and maintain strong working relationships with investigators and research teams
Conduct site evaluations, site initiation visits, monitoring visits, and site close-out visits in compliance with study protocols and regulatory guidelines
Ensure clinical trials follow Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and company standard operating procedures
Support and train investigators and site staff on study protocols, patient treatment procedures, and clinical trial objectives
Monitor patient recruitment, retention, and protocol compliance to ensure successful trial execution
Identify potential risks or compliance issues at research sites and implement corrective or preventive actions
Ensure accuracy, completeness, and timely submission of clinical trial data and safety reports
Collaborate with internal teams including research and development stakeholders and central monitoring teams
Mentor and support junior clinical research associates and assist with their onboarding and professional development
Assist in identifying and evaluating new investigators or clinical sites for future research studies

Required Qualifications

Educational Requirements:
Bachelor’s degree or equivalent in a health-related field such as medical science, nursing, pharmacy, or life sciences

Experience and Skills:
Minimum of three years of clinically related experience including at least two years of independent clinical trial monitoring experience
Experience monitoring investigational drug or medical device trials
Strong knowledge of oncology clinical research
Understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements
Ability to interpret clinical trial protocols and apply scientific principles to trial conduct
Strong communication, presentation, and stakeholder management skills
Ability to manage multiple projects and deadlines in a fast-paced environment
Experience mentoring or guiding junior clinical research professionals
Strong analytical and problem-solving abilities

Salary Insights
The company has not publicly disclosed the specific salary range for this position in the job description. Compensation typically depends on experience, geographic location, and organizational policies. Employees may also receive performance incentives, bonuses, and comprehensive benefits packages.

Company Overview
AbbVie is a global research-driven biopharmaceutical company dedicated to discovering and delivering innovative medicines that address serious health conditions. The company focuses on several key therapeutic areas including immunology, oncology, and neuroscience, along with products and services within its Allergan Aesthetics portfolio. Through scientific research and collaboration, the organization aims to improve patient outcomes and develop therapies that address unmet medical needs worldwide.

FAQs
Where is the job located?
Colorado, United States (candidates must reside in Colorado)

Is the role remote?
The role is remote-based but requires travel to clinical research sites

What therapeutic area does the role focus on?
Oncology clinical trials

What experience is required?
At least three years of clinical research experience including clinical trial monitoring

Application Tips
Highlight experience in clinical trial monitoring and site management
Demonstrate knowledge of GCP, ICH guidelines, and regulatory compliance
Include experience working with investigators, clinical sites, and research teams
Showcase oncology research experience if applicable
Emphasize project management, analytical thinking, and communication skills relevant to clinical research roles