At a Glance
- Tasks: Lead global clinical trials and manage project deliverables with a dynamic team.
- Company: Join Medpace, a leading clinical research organisation focused on innovative medical therapies.
- Benefits: Enjoy competitive pay, health benefits, and opportunities for professional growth.
- Other info: Collaborative culture with mentorship and clear career advancement paths.
- Why this job: Make a real impact in healthcare by advancing clinical research and improving patient outcomes.
- Qualifications: Bachelor's degree in health/life sciences and 2+ years of clinical trial management experience.
The predicted salary is between 82800 - 101200 $ per year.
Medpace is currently looking for an experienced Clinical Trial Manager (CTM) to lead global clinical research studies. Medpace is a scientifically led organization offering full-service solutions for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. The Clinical Trial Manager position is the lead role for multiservice global/regional clinical trials. The CTM interacts with sponsors and sites and manages the timeline and project deliverables (minus finance). This role coordinates all services contracted for the study, leading the cross functional team through all life cycles of the project (from startup to database lock and closure). CTM will attend bid defense meetings and support business development activities, as needed. This position is office based.
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 project-specific issues and study deliverables.
- Maintain in depth knowledge of protocol, therapeutic area, and indication.
- Provide cross-functional oversight of 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 mitigations.
- Manage study vendors.
- Manage site quality, including direct supervision of project Clinical Research Associates (CRA) and monitoring deliverables.
Qualifications
- Bachelor’s degree or above in health/life science related field.
- At least two years of clinical trial management experience in the Asia Pacific region; indications of interest a plus.
- Prior CRO experience is preferred.
- Excellent communication skills including good verbal and written English.
- Flexible, accountable, and comfortable working in a global environment.
Other Employee Benefits
- Competitive compensation programs that recognize and reward performance.
- Comprehensive health, wellness, retirement, and PTO benefits.
- Office based culture with occasional WFH that provides flexibility for eligible positions after training.
- Company-sponsored social events.
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 in Melbourne employer: Medpace
Medpace is an exceptional employer, offering a dynamic work environment in Melbourne that fosters professional growth and development within the clinical research field. With a strong focus on employee well-being, competitive compensation, and flexible working arrangements, Medpace supports its team members in achieving their career aspirations while contributing to meaningful advancements in medical therapeutics. Join a globally recognized leader in the CRO industry, where your expertise will be valued and your contributions will make a real impact.
