Clinical Records Administrator
4 weeks ago
We are seeking a detail-oriented and organized Clinical Records Administrator to join our team at Medpace. In this role, you will be responsible for ensuring the integrity of our Trial Master File (TMF) by managing electronic documents, tracking and maintaining quality checks, and communicating with internal associates globally.
Responsibilities:- Manage electronic filing system for trial documentation
- Track, maintain, and perform quality check of electronic documents
- Communicate with internal associates globally regarding the TMF
- Prepare documents for shipment
- High school diploma or equivalent
- Experience in document administration
- High attention to detail
- Exemplary organizational skills
- Strong written and verbal communication skills
- Knowledge of MS Office (Excel and Outlook)
Medpace is a full-service clinical contract research organization (CRO) that provides 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.
As a Clinical Records Administrator at Medpace, you will have the opportunity to work with a team of experienced professionals and contribute to the success of our clinical trials. If you are a detail-oriented and organized individual with a passion for document administration, we encourage you to apply for this exciting opportunity.
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Clinical Research Administrator
4 weeks ago
Cincinnati, Ohio, United States Medpace Full timeClinical Research AdministratorMedpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are seeking a Clinical Research Administrator to support TMF oversight for a trial by ensuring documents meet established quality...
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Cincinnati, Ohio, United States University of Cincinnati Full time**Job Overview**The University of Cincinnati's Office of Clinical Research is seeking a highly skilled Clinical Trial Administrator to join their team. This role will work closely with various teams within the office to facilitate the start of clinical research studies.The selected candidate will be responsible for reviewing, redlining, and negotiating...
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Clinical Research Coordinator
4 weeks ago
Cincinnati, Ohio, United States Medpace Full timeClinical Records Administrator**Job Summary**Medpace is seeking a Clinical Records Administrator to support the Trial Master File (TMF) oversight for a trial. The successful candidate will ensure documents meet established quality standards, manage electronic filing systems, track and maintain electronic documents, communicate with internal associates, and...
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