Clinical Trial Manager II
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Clinical Trial Manager II – Onsite role in Cincinnati, OH | Duration : Fulltime Job Description: Responsibilities
- • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/Google Cloud Platform and all other applicable laws, rules, and regulations
- • Serve as primary Sponsor contact for operational project-specific issues and study
- • 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.
- Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
- Experience in Phases II.
- 5+ years as a Clinical trial manager within a CRO.
- Management of overall project timeline
- A life science degree.
- Many years’ experiences in Medpace Therapeutic Areas (TA) which are: Onc./Hem, Cardio/Renal/Metabolism, Neuro &Infectious Disease, Rare Disease, Ophthalmology, Allergy/Asthma, Devices – we prefer depth of TA experience over breath of TA experience,
- Good career development (timely progression and quality of work assignments), predominately with large, well established CROs (we use the top 10 US CROs as our benchmark),
- Significant time with each organization when a permanent employee (2-3 years minimum and longer is better).