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

Syneos Health, Inc.; Kansas; Remote; USD 60,000 - 80,000; Full time

Job summary

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate II to monitor clinical studies ensuring compliance with Good Clinical Practice. The candidate should have a relevant degree and 2-4 years of clinical research monitoring experience. This role involves collaborating with cross-functional teams and ensuring accurate documentation. Offering competitive benefits including health care and a 401(k).

Benefits

Company car or car allowance

Health benefits (medical, dental, vision)

401(k) with company match

Flexible paid time off

Qualifications

• Minimum of 2-4 years of experience in clinical research monitoring.
• Strong knowledge of GCP guidelines and regulatory requirements.
• Proficiency in using relevant software.

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

Good Clinical Practice (GCP)

Communication skills

Analytical skills

Teamwork

Organizational skills

Education

Bachelor's degree in a related field

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Overview

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

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. We collaborate across functional areas and environments to simplify and streamline work, aiming to accelerate delivery of therapies and change lives.

We are a global organization with 29,000 employees across 110 countries, committed to building a diverse and inclusive workplace where work 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 participation 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 and Additional Information

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 varies by location in accordance with applicable laws. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range: The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on factors such as the candidate’s qualifications and proficiency for the role.

About 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 require reasonable accommodation to complete any part of the application process, please contact us at [e-mail].

Legal and Compliance

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks as needed. This content is intended to comply with applicable laws and is not a contract. The Company is committed to compliance with the Americans with Disabilities Act, including reasonable accommodations when appropriate.