Clinical Trial Manager
Clinical Trial Manager
Posted on :
15-03-2025
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1 Vacancy
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Job Description
Job Title: Clinical Trial Manager (Nephrology)
Job Location: London UK
Job Location Type: Onsite
Job Contract Type: Fulltime
Job Seniority Level:
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility only with relevant experience. We offer a very competitive salary/bonus program plus equity grants which have become very lucrative for our associates.
Responsibilities
Medpace is a fullservice clinical contract research organization (CRO). We provide Phase IIV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology cardiology metabolic disease endocrinology central nervous system antiviral and antiinfective. Headquartered in Cincinnati Ohio employing more than 5000 people across 40 countries.
Why Medpace
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
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
Responsibilities
- Manage and provide accountability for daytoday 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 projectspecific issues and study deliverables
- Maintain in depth knowledge of protocol therapeutic area and indication
- Provide crossfunctional oversight of internal project team members and deliverables which includes ensuring all necessary projectspecific 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
- Responsible for management of study vendor
- Manage site quality including direct supervision of project Clinical Research Associates and monitoring deliverables
- Bachelor’s degree in a health or life sciencerelated field; Advanced degree in a health or life sciencerelated field preferred;
- Experience in Phases 14; Phases 23 preferred;
- Minimum of 5 years of Clinical Trial Management experience CRO experience preferred;
- 5 years of Project Manager/Clinical Trial Manager experience at a CRO required for a remotebased role;
- Management of overall project timeline;
- Bid defense experience preferred; and
- Strong leadership skills.
Medpace is a fullservice clinical contract research organization (CRO). We provide Phase IIV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology cardiology metabolic disease endocrinology central nervous system antiviral and antiinfective. Headquartered in Cincinnati Ohio employing more than 5000 people across 40 countries.
Why Medpace
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Companysponsored employee appreciation events
- Employee health and wellness initiatives
- Recognized by Forbes as one of America's Most Successful Midsize Companies inand 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise quality capabilities reliability and compatibility
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
https://lifelancer/jobs/view/b114fb05156e747d52af61298e12564d
Employment Type
Full Time
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