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Cra Ii/ Scra I

3 weeks ago

Sydney, New South Wales, Australia Buscojobs Full time

CRA II / SCRA I (Melbourne / Sydney Home based)
Updated :August 1, 2025
Location :Adelaide, SA, Australia
Job ID :25100922
Description
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 market realities.
Our Clinical Development model centers on the customer and patient, aiming to simplify and streamline our work to make Syneos Health both easier to work with and for.
Whether 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.
We are agile and driven to accelerate therapy delivery because we are passionate about changing lives.
Discover what our 29,000 employees across 110 countries already know:WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We develop our people through career growth, supportive management, training, peer recognition, and rewards.
We foster a Total Self culture where authenticity is valued, and we care for our people.
We embrace diversity to create a welcoming environment where everyone belongs.
Job Responsibilities
Conduct on-site and remote monitoring of clinical studies to ensure compliance with GCP and other regulations.
Develop tools, procedures, and processes for quality monitoring, including plans and checklists.
Contribute to SOP and training material development, implementation, and delivery.
Manage project components such as site visits, study tracking, and issue resolution.
Document monitoring activities accurately and timely, including reports and follow-up actions.
Collaborate with investigators, site staff, and stakeholders to support trial operations.
Qualifications
Bachelor's degree or equivalent experience in a related field.
2-4 years of clinical research monitoring experience.
Strong knowledge of GCP and regulatory requirements.
Excellent communication and interpersonal skills.
Ability to work independently and manage multiple priorities.
Proficiency with clinical trial management systems and relevant software.
Certifications
CCRA or equivalent certification preferred.
Necessary Skills
Attention to detail, analytical skills, problem-solving, and critical thinking.
Effective team collaboration, organizational, and time management skills.
Proficiency in Microsoft Office Suite.
This posting is for future opportunities; by expressing interest, you'll be added to our talent pipeline for consideration when roles open.
Get to know Syneos Health
We have worked with 94% of FDA-approved drugs, 95% of EMA-authorized products, and over 200 studies globally.
Join us to make a difference in patients' lives worldwide.
Learn more about us.
Additional Information
Responsibilities listed are not exhaustive.
The company may assign other duties at its discretion.
Qualifications may be considered equivalent.
Nothing herein creates an employment contract.
We comply with all applicable legislation, including the EU Equality Directive and the Americans with Disabilities Act, providing reasonable accommodations when needed.
Summary
Roles at the P21 level in Clinical Monitoring / CRA are responsible for ensuring the conduct of clinical studies according to accepted practices, including monitoring, developing tools, and managing project components.
These roles impact the quality and integrity of clinical research, contributing to medical advancements and patient outcomes.
Conduct thorough on-site and remote monitoring.
Develop and implement quality tools and processes.
Manage project components within their responsibility.
Apply professional knowledge obtained through education and experience.
Maintain high standards to ensure successful clinical trials.
Working here matters, as we strive to bring therapies to those in need.
A career with Syneos Health offers the chance to improve lives worldwide, with a commitment to diversity, equity, and inclusion.
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