Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide 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 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, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Responsibilities:
* Become familiar with ICH-GCP guidelines, industry regulations, and Medpace systems;
* Complete training to become familiar with the Contracts Specialist role;
* Provide day to day departmental support activities as necessary; Examples include but are not limited to customising budget excels and payment schedules, critically evaluating budgetary requests in relation to study protocol requirements, assisting with preparation of budget escalation tools, providing quality control check and formatting assistance as necessary;
* Assist in drafting Clinical Trial Agreement Amendments;
* Uploading fully executed agreements to appropriate SharePoint and eTMF locations;
* Maintain database/spreadsheets and compile reports as necessary to facilitate tracking/documentation of departmental activities;
* Conduct quality control reviews of departmental documents as necessary;
* Support other departments on ad hoc projects; and
* Perform other administrative tasks as needed
Qualifications:
* Working towards a degree in a Life Science related field.
* Excellent skills in Microsoft Word, Excel, and Outlook.
* Candidate should have done some research into what a Contracts Specialist job entails.
Share this job:
Share this Job