Clinical Research Associate II - Full Service - Oncology (Home-Based in Central US)

Syneos Health, Inc.; Kentucky; Remote; USD 75,000 - 95,000; Full time

Job summary

A leading biopharmaceutical solutions organization seeks a Clinical Research Associate II to perform on-site and remote monitoring of clinical studies. The position requires a Bachelor's degree and 2-4 years of experience in clinical research monitoring with a strong understanding of GCP guidelines. Responsibilities include ensuring compliance, developing monitoring tools, and collaborating with cross-functional teams. The role offers a competitive salary and benefits.

Benefits

Health benefits (medical, dental, vision)

401(k) with company match

Flexible paid time off

Employee Stock Purchase Plan

Qualifications

• Minimum of 2-4 years of experience in clinical research monitoring.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Ability to work independently and manage multiple priorities.

Responsibilities

• Conduct on-site and remote monitoring of clinical research studies.
• Develop and implement tools for quality monitoring.
• Manage defined components of projects or processes.

Skills

Attention to detail

Strong analytical skills

Problem-solving abilities

Strong communication skills

Teamwork

Education

Bachelor's degree in a related field

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Clinical Research Associate II - Full Service - Oncology (Home-Based in Central US)

Updated: September 19, 2025
Location: USA-KY-Remote
Job ID:25101618

Overview

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model centers the customer and patient experience, with a focus on simplifying and streamlining work to better support customers and teams.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies because we are motivated to change lives.

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We develop our people through career development and progression, supportive line management, training, peer recognition and total rewards.
• We are committed to our Total Self culture, uniting us globally and prioritizing the well‑being of our people.
• We value diversity of thoughts, backgrounds, cultures, and perspectives to foster belonging.

Job Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices, including review of study protocols, informed consent forms, and case report forms.
• Develop and implement tools, procedures, and processes to ensure quality monitoring, such as monitoring plans, checklists, and templates.
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including SOPs and training materials.
• Manage defined components of projects or processes, such as coordinating site visits, tracking study progress, and resolving issues.
• Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans.
• Collaborate with cross-functional teams to support clinical trial operations, including interaction with investigators and site staff to ensure smooth study conduct.

Qualifications

• Bachelor's degree in a related field or equivalent experience
• Minimum of 2-4 years of experience in clinical research monitoring
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
• Excellent communication and interpersonal skills
• Ability to work independently and manage multiple priorities
• Proficiency in using clinical trial management systems and other relevant software

Certifications

• Certified Clinical Research Associate (CCRA) or equivalent certification preferred

Necessary Skills

• Attention to detail and strong analytical skills
• Problem-solving abilities and critical thinking
• Ability to work effectively in a team environment
• Strong organizational and time management skills
• Proficiency in Microsoft Office Suite

Benefits and Compensation

The position may include a company car or car allowance, health benefits (medical, dental, vision), 401(k) with company match, eligibility to participate in Employee Stock Purchase Plan, eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Paid sick time eligibility varies by state and municipality; Syneos complies with applicable laws.

Salary Range: The base salary range represents the anticipated range for this position. Actual salary varies based on qualifications, skills, competencies, and proficiency.

Get to know Syneos Health

Syneos Health (Nasdaq: SYNH) is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affairs and commercial insights into outcomes to address modern market realities. We support a diverse, equitable and inclusive culture. Learn more at http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks at its sole discretion. Equivalent experience, skills, and/or education will be considered. The Company will determine what constitutes equivalent qualifications. This description is intended to comply with applicable laws and obligations, including the Americans with Disabilities Act, with reasonable accommodations when appropriate.

Summary

Roles within Clinical Monitoring/CRA at the P21 level are responsible for ensuring that clinical studies are conducted in accordance with widely accepted clinical practices. Responsibilities include on-site and remote monitoring, tool and process development for quality monitoring, and contributing to the design and delivery of programs and policies. These roles may involve managing two or fewer employees and emphasize professional/technical contribution and collaboration to support successful trials.

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability, or any legally protected status. If accommodations are required for the application process, please contact [e-mail].