CRA II/ SCRA I

Overview

Updated: September 2, 2025
Location: NZL-Remote
Job ID:

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, and we strive to simplify and streamline work to improve both our experience and that of our customers. We offer opportunities in Functional Service Provider partnerships or Full-Service environments, collaborating with passionate problem solvers to accelerate the delivery of therapies and change lives.

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

Get to know Syneos Health

• We are passionate about developing our people through career development, progression, training, peer recognition and total rewards programs.
• We maintain our Total Self culture, uniting us globally and taking care of our people.
• We strive to build the company and a workplace where diverse thoughts, backgrounds, cultures and perspectives are valued and everyone belongs.

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 (e.g., monitoring plans, checklists, templates).
• Contribute to design, implementation and delivery of processes, programs and policies, including 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).
• Document monitoring activities and findings accurately and timely (e.g., monitoring reports, follow-up letters, action plans).
• Collaborate with cross-functional teams to support clinical trial operations, including 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, strong analytical and problem-solving skills.
• Ability to work effectively in a team and manage time.
• Strong organizational and time management skills; proficiency in Microsoft Office Suite.

Summary

Roles within the Clinical Monitoring/CRA job family at the P21 level are responsible for conducting on-site and remote monitoring to ensure adherence to clinical practices, developing monitoring tools and processes, and contributing to program design and delivery. These roles may involve individual contributors and may manage two or fewer employees.

Legal and Employment Information

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway. We also invite you to join our Talent Network to stay connected to opportunities. 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 us at: Email:

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