Clinical Research Associate II / Sr CRA - Full Service - ONC + Gen Med (Home-Based in Central US)

Syneos Health, Inc.; Location (WV); Remote; USD 70,000 - 127,000; Full time

Job summary

A leading biopharmaceutical solutions organization seeks a Clinical Research Associate II/Sr CRA to conduct on-site and remote monitoring of clinical studies. The ideal candidate has a Bachelor's degree, 2-4 years of clinical research experience, and strong communication skills. This position offers competitive benefits and a salary range of $70,100 - $126,100 depending on qualifications.

Benefits

Health benefits (medical, dental, vision)

401(k) with company match

Flexible paid time off (PTO)

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, procedures, and processes for quality monitoring.
• Ensure accurate and timely documentation of monitoring activities.

Skills

Attention to detail

Analytical skills

Problem-solving abilities

Excellent communication

Interpersonal skills

Organizational skills

Time management

Education

Bachelor's degree in a related field

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Overview

Description

Clinical Research Associate II / Sr CRA - Full Service - ONC + Gen Med (Home-Based in Central US) – Updated September 22, 2025. Location: USA-WV-Remote. Job ID: 25101627.

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 the patient, and we strive to simplify and streamline work to be easier to engage with and to work for.

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

Why Syneos Health

• We are committed to developing our people through career development, training, and rewards; supportive management; and total rewards programs.
• We foster a Total Self culture where you can authentically be yourself, uniting us globally and supporting our people.
• We build a diverse, inclusive environment where different perspectives help everyone belong.

Job Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted 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 (e.g., monitoring plans, checklists, templates).
• Contribute to the design and delivery of processes, programs, and policies, including SOP development and training materials.
• Manage defined components of projects or processes within the area of responsibility (e.g., coordinating site visits, tracking study progress, resolving issues).
• Ensure accurate and timely documentation of monitoring activities and findings (e.g., monitoring reports, follow-up letters, action plans).
• Collaborate with cross-functional teams to support clinical trial operations (investigators, site staff, and other stakeholders) 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 & Salary

The benefits for this position may include a company car or car allowance, health benefits (medical, dental, vision), 401(k) with company match, eligibility to participate in an 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 location. Syneos complies with all applicable paid sick time requirements.

Salary Range: $70,100.00 - $126,100.00. The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of Novel FDA approved drugs, 95% of EMA authorized products, and conducted over 200 studies across 73,000 sites and 675,000+ trial patients.

No matter your role, you’ll take initiative and challenge the status quo in a dynamic environment. Learn more about Syneos Health at http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities are not exhaustive. The company may assign other tasks as needed. Equivalency of experience, skills, and education will be considered. The information herein is subject to applicable laws and may be updated without notice. The company is committed to compliance with the Americans with Disabilities Act and will provide reasonable accommodations as needed during the application process.

Summary

Roles within the Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring clinical studies are conducted in accordance with clinical practices, including on-site and remote monitoring, and development of monitoring tools and procedures. These roles may manage two or fewer staff and focus on contributing to process design, implementation, and delivery.

At Syneos Health, we value a diverse, inclusive, and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply and consider transferrable skills. You may also join our Talent Network to stay connected to opportunities.

Syneos Health (Nasdaq: SYNH) is a leading integrated biopharmaceutical solutions organization dedicated to accelerating customer success and delivering therapies to patients. We support a diverse, equitable and inclusive culture. Contact: Phone [phone] | Fax [phone] | Toll-Free 866-462-7373

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 other legally protected status. If you require reasonable accommodations to apply, please contact [e-mail].