Clinical Trial Manager
Há 2 dias
As a Clinical Trial Manager at Medpace, you will be responsible for managing and providing 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.
You will serve as the primary Sponsor contact for operational project-specific issues and study deliverables, maintaining in-depth knowledge of protocol, therapeutic area, and indication.
Additionally, you will provide cross-functional oversight of internal project team members and deliverables, ensuring all necessary project-specific training is provided.
You will 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, and be responsible for management of study vendor.
Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
RequirementsTo be successful in this role, you will need a Bachelor's degree in a health-related field, with an advanced degree in a health-related field preferred.
You will have experience in Phases 1-4, with Phases 2-3 preferred, and at least 5 years as a project/clinical trial manager within a CRO.
Strong leadership skills and fluency in English are also required.
About MedpaceMedpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.
Headquartered in Cincinnati, Ohio, we employ over 5,000 people across 40+ countries.
Why Medpace?At Medpace, we are passionate about making a difference in the lives of patients and families affected by disease.
We offer a competitive compensation and benefits package, as well as opportunities for professional growth and development.
Join us in our mission to accelerate the development of safe and effective medical therapeutics.
", "requirements": "- Bachelor's degree in a health-related field
- Advanced degree in a health-related field preferred
- Experience in Phases 1-4
- At least 5 years as a project/clinical trial manager within a CRO
- Strong leadership skills
- Fluency in English
- Competitive compensation and benefits package
- Opportunities for professional growth and development
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.
Headquartered in Cincinnati, Ohio, we employ over 5,000 people across 40+ countries.
", "why_medpace": "At Medpace, we are passionate about making a difference in the lives of patients and families affected by disease.
We offer a competitive compensation and benefits package, as well as opportunities for professional growth and development.
Join us in our mission to accelerate the development of safe and effective medical therapeutics.
", "contact_info": "A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
", "EO/AA_Employer": "EO/AA Employer M/F/Disability/Vets
", "job_id": "#J-18808-Ljbffr"}-
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