Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We provide remote flexibility with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
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
***We kindly ask that you send your CV in English***
* Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
* Experience in Phases 1-4; Phases 2-3 preferred
* 5+ years as a project/clinical trial manager within a CRO; required for home-based
* Management of overall project timeline
* Strong leadership skills
* Fluency in English
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
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