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

Syneos Health, Inc.; Ohio; Remote; USD 70,000 - 127,000; Full time

Job summary

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate II/Sr CRA to conduct and monitor clinical studies. The role is home-based in Central US and requires a Bachelor's degree with 2-4 years of clinical research monitoring experience. Candidates should have strong knowledge of GCP guidelines and excellent communication skills. This position offers a salary range from $70,100 to $126,100 along with various benefits.

Benefits

Company car or car allowance

Health benefits (medical, dental, vision)

401(k) with company match

Employee Stock Purchase Plan

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 on-site and remote monitoring of clinical research studies.
• Develop and implement tools and procedures for quality monitoring.
• Collaborate with cross-functional teams to support clinical trial operations.

Skills

Attention to detail

Strong analytical skills

Problem-solving abilities

Effective in team environment

Strong organizational skills

Time management skills

Education

Bachelor's degree in related field

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Overview

Updated: September 22, 2025
Location: USA-OH-Remote
Job ID: 25101627

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

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

Compensation and Benefits

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

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 the 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 may vary by location in accordance with state and municipal regulations. Syneos complies with applicable federal, state, and municipal paid sick time requirements.

Get to know Syneos Health: 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. Equal consideration will be given to all qualified applicants; transferrable skills are encouraged. We invite you to join our Talent Network to stay connected to additional career opportunities.

Syneos Health (Nasdaq: SYNH) 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 accommodation to complete the application process, please contact [e-mail].