CRA II

Overview

Updated:
Yesterday

Location:

USA-ND-Remote
Job :

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, continuously seeking ways to simplify and streamline work to be 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 to help our customers achieve their goals.

Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE

• 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 – authentic and inclusive. We take care of our people.
• We are building a diverse, inclusive culture where everyone feels they belong.

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices, including reviewing study protocols, informed consent forms, and case report forms.
• Develop and implement tools, procedures, and processes to ensure quality monitoring (monitoring plans, checklists, templates).
• Contribute to the design, implementation, and delivery of processes, programs, and policies; participate in development of SOPs 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 (monitoring reports, follow-up letters, action plans).
• Collaborate with cross-functional teams to support clinical trial operations (investigators, site staff, and other stakeholders) for smooth study conduct.

• 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

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

• 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

The benefits for this position may include a company car or car allowance, health benefits (Medical, Dental and 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 location. Syneos complies with applicable paid sick time requirements.

Salary Range: $70,100.00 - $

Over the past 5 years, we have worked with 94% of novel FDA approved drugs, 95% of EMA authorized products and over 200 studies across 73,000 sites and 675,000+ trial patients. Learn more about Syneos Health at

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 complete any part of the application process, please contact