At a Glance
- Tasks: Manage clinical trials and ensure project success in a dynamic environment.
- Company: Join Medpace, a leading CRO dedicated to advancing medical research.
- Benefits: Enjoy competitive pay, health benefits, and opportunities for professional growth.
- Other info: Collaborative culture with ongoing training and clear career advancement paths.
- Why this job: Make a real impact on patient outcomes while working with top experts.
- Qualifications: Bachelor's degree and 2+ years of clinical trial management experience required.
The predicted salary is between 82800 - 101200 $ per year.
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Melbourne, Australia. Clinical Trial Managers with expertise in Cardiovascular, Renal, Metabolic or Gastrointestinal related are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.
Responsibilities
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
- Maintain in depth knowledge of protocol, therapeutic area, and indication;
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
- Develop operational project plans;
- Manage risk assessment and execution;
- Responsible for management of study vendor;
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Qualifications
- Bachelor’s degree in a health or life science-related field;
- At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
- Experience in Cardiovascular, Renal, Metabolic or Gastrointestinal related studies required;
- Excellent communication skills including good written and spoken English;
- Flexible, accountable and comfortable in working in a global environment.
Why Medpace?
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.
- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Office based environment with on-site mentors and defined career paths with clear advancement opportunities.
- Competitive compensation programs that recognize and reward performance.
- Comprehensive health, wellness, retirement, and PTO benefits.
Please note benefits may vary based on country.
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Clinical Trial Manager employer: Medpace, Inc.
Medpace is an exceptional employer for those looking to launch their careers in clinical trial management, particularly in the vibrant city of Melbourne. With a strong focus on employee growth, Medpace offers comprehensive training programs, clear career advancement paths, and a collaborative work culture that fosters innovation and open communication. Employees benefit from competitive compensation, health and wellness programs, and a supportive environment that encourages professional development and meaningful contributions to advancing medical therapeutics.
