Clinical Trial Manager I/ II- Melbourne

Updated: October 23, 2025
Location: AUS-Client
Job ID: 25102743

Overview

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 the patient, continuously seeking ways to simplify and streamline our work. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers and innovate as a team to help our customers achieve their goals.

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

Job Responsibilities

- Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executed

- Implement clinical research protocols and ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines

- Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to facilitate smooth communication and coordination

- Plan and manage logistics and resource usage for clinical trials, including scheduling, budgeting, and resource allocation

- Track study progress and ensure alignment with project milestones, client deliverables, and budget, providing regular updates to stakeholders

- Prepare and present study reports and updates to stakeholders, including detailed analysis of study data and progress

- Ensure adherence to global and regional regulations and guidelines, staying up-to-date with changes or updates

- Provide guidance and support to lower-level professionals and team members, fostering a collaborative and supportive work environment

- Identify and resolve issues or challenges that arise during the course of the study, ensuring timely and effective solutions

- Maintain accurate and comprehensive documentation of all study-related activities, ensuring transparency and accountability

Qualifications

- Bachelor's degree in a related field (e.g., life sciences, clinical research)

- Minimum of 3 years of experience in clinical trial management or a related field

- In-depth knowledge of clinical research processes and regulations

- Strong project management and organizational skills

- Excellent communication and interpersonal skills

- Ability to work independently and as part of a team

- Proficiency in using clinical trial management software and tools

Certifications

- Certified Clinical Research Professional (CCRP) or equivalent certification preferred

Necessary Skills

- Strong analytical and problem-solving skills

- Attention to detail and accuracy

- Ability to manage multiple projects and priorities simultaneously

- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)

- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

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

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks and responsibilities at its sole discretion. Qualifications may differ from those listed, and equivalent experience, skills, and/or education will be considered. The Company will determine what constitutes as equivalent to the described qualifications. Nothing herein should be construed as an employment contract. The Company is committed to compliance with applicable disability laws and providing reasonable accommodations, where appropriate, to assist employees or applicants to perform essential functions.

Summary

Roles within the Clinical Trial Management job family at the P22 level oversee the development, coordination, and implementation of Phase 1 clinical research studies. They collaborate with the principal investigator, serve as liaisons between research subjects, client teams, investigators, and clinic operations teams, and meticulously plan logistics and resource usage. These roles track study progress in alignment with project milestones, client deliverables, and budget, while ensuring compliance with global and regional regulations.

Contact and Equality

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 during the application process, please contact jobs@syneoshealth.com.

Phone: 919 876 9300
Fax: 919 876 9360
Toll-Free: 866 462 7373

Syneos Health is committed to an inclusive, diverse, and authentic workplace.

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