CRA II

Syneos Health, Inc.; Town of Texas (WI); Remote; USD 70,000 - 127,000; Full time

Job summary

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate to conduct monitoring of clinical research studies. This role involves developing monitoring tools, ensuring compliance with GCP guidelines, and collaborating with cross-functional teams. Ideal candidates will have a related Bachelor's degree and 2-4 years of experience in clinical research. The position offers a competitive salary range and a supportive work environment.

Benefits

Flexible paid time off

Health benefits

401(k) with company match

Employee Stock Purchase Plan

Commissions/bonus based on performance

Qualifications

• 2-4 years of experience in clinical research monitoring.
• Strong knowledge of Good Clinical Practice (GCP) guidelines.
• Excellent communication and interpersonal skills.

Responsibilities

• Conduct monitoring of clinical research studies for compliance.
• Develop tools and procedures for quality monitoring.
• Collaborate with cross-functional teams for study support.

Skills

Attention to detail

Strong analytical skills

Problem-solving abilities

Effective teamwork

Strong organizational skills

Time management skills

Education

Bachelor's degree in a related field

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Updated: September 24, 2025
Location: USA-TX-Remote
Job ID: 25101620

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

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 passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. When we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
• Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
• Manage defined components of projects or processes within the area of responsibility, 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 working with 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

Environment and culture that supports our people to thrive, develop and advance. Benefits 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, flexible paid time off (PTO) and sick time. Paid sick time eligibility varies by location in compliance with applicable laws. Syneos complies with all federal, state, and municipal 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 various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health

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 are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at: Email: [e-mail]

Phone: [phone] | Fax: [phone] | Toll-Free: 866-462-7373