Associate Clinical Trial Manager - Renal
Associate Clinical Trial Manager - Renal
Posted on :
15-03-2025
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1 Vacancy
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Job Description
Job Title: Associate Clinical Trial Manager (PhD) Renal
Job Location: London UK
Job Location Type: Onsite
Job Contract Type: Fulltime
Job Seniority Level:
Medpace is currently seeking candidates with Renal related PhDs and/or PostDoctoral Research experience for a fulltime officebased Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
A fantastic opportunity for recent PhD graduates to enter the industry receive solid foundational training work in an international environment and develop their career in the research and development of cuttingedge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
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
A fantastic opportunity for recent PhD graduates to enter the industry receive solid foundational training work in an international environment and develop their career in the research and development of cuttingedge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
Responsibilities
- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
- Compile and maintain projectspecific status reports within the clinical trial management system
- Interact with the internal project team Sponsor study sites and thirdparty vendors
- Provide oversight and quality control of our internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
- PhD in Life Sciences
- Fluency in English with solid presentation skills
- Ability to work in a fastpaced dynamic industry within an international team
- Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
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/5a11f3472cfa644206bcdbcd
Employment Type
Full Time
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