Job Title: Clinical Trial Manager
Job Description:
* 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.
Required Skills and 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.
Benefits:
* Flexible work environment.
* Competitive compensation and benefits package.
* Competitive PTO packages.
* Structured career paths with opportunities for professional growth.
* Company-sponsored employee appreciation events.
* Employee health and wellness initiatives.
Others:
* Medpace is a full-service clinical contract research organization.
* Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
* Join us today!