Cra Ii/ Scra I

Updated: September 2, 2025
Location: Adelaide, SA, Australia
Job ID: 25000423
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.
Why?
Because 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
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.
Learn more about Syneos Health.
Additional information is available at:
Summary
Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices.
This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring.
These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees.
The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education.
Impact and Contribution
Roles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies.
By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results.
They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials.
Their contributions are essential for advancing medical knowledge and improving patient outcomes.
Core Focus
Conduct thorough on-site and remote monitoring of clinical research studies
Develop and implement tools, procedures, and processes to ensure quality monitoring
Manage defined components of projects or processes within their area of responsibility
Utilize practical knowledge of a professional area, typically obtained through education combined with experience
Maintain high standards of clinical practice and ensure the success of clinical trials
Discover what our more than 29,000 employees already know: work here matters everywhere.
We work hard, and smart, all in the name of getting much-needed therapies to those who need them most.
A career with Syneos Health means your everyday work improves patients' lives around the world.
Syneos Health (Nasdaq:SYNH) 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.
Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients.
We support a diverse, equitable and inclusive culture.
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