Medpace Jobs & Careers

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20 Medpace jobs found on Monster.

Jobs 1 to 20 of 20
DESCRIPTION OF JOB DUTIES Develop and maintain validation deliverables for Medpace computer systems; Develop and execute validation plans and test cases; Assist with Administration of Microsoft Team Foundation Server; Write validation report for Medpace computer systems; Implement tools and procedures to facilitate and automate validation and documentation processes; and Participate in sponsor aud...
SUMMARY OF POSITION The Regulatory Affairs Manager plays a key role in our regulatory processes at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Working onsite at Medpace global headquarters in Cincinnati, Ohio the Regulatory Affairs Manager is an integral part of the drug devel...
As a paid, full-time senior intern you will have the opportunity to work within our Regulatory Submissions group, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with the regulatory submissions team, you will gain valuable hands on experience to enable you to...
SENIOR ACCOUNTANT DESCRIPTION OF JOB DUTIES Oversee monthly close process through preparation and review of journal entries, account reconciliations, and supporting schedules, includes performing account analysis, investigation and issue resolution Prepare monthly balance sheet and income statement analysis to provide understanding and account knowledge to assist with budgeting and forecasting Pre...
SUMMARY OF POSITION The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivaled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportun...
Location: Cincinnati, OH or Dallas, TX DESCRIPTION OF JOB DUTIES Efficiently manage and successfully execute all aspects of global start-up according to Sponsor specifications; Perform quality checks on submission documents and site essential documents; Interact with US central IRBs, sites, and international associates; Prepare and approve informed consent forms; Review pertinent regulations to de...
Location: Cincinnati, Minneapolis, and Dallas Medpace is a global, full-service clinical research organization with therapeutic specialization in oncology, cardiovascular, endocrine/metabolic, Infectious disease and CNS. We have steadily expanded operations in nearly forty countries. Headquarters are located in Cincinnati, Ohio and we are currently seeking a Clinical Safety Manager in that office,...
Medpace Reference Laboratories is currently seeking a Project Coordinator to join our Sample Management Team. This individual will be responsible for day-to-day project start-up activities, as well as the coordination of laboratory shipments. DESCRIPTION OF JOB DUTIES Maintain study-related documents; Ensure that all aspects of designated clinical protocol are in accordance with project timelines,...
Medpace is a growing Contract Research Organization (CRO) with headquarters located in Cincinnati, Ohio. As a global leader in research-based drug and device development, Medpace builds strong strategic partnerships with select sponsors to achieve the most efficient and cost-effective path to drug and device approval. Our offices in the United States are growing rapidly and we have an exciting opp...
DESCRIPTION OF JOB DUTIES Develop and validate new assay methods; Design protocols and create study reports; and Supervise all phases of bioassays to support human pharmacokinetics and ADME studies. QUALIFICATIONS/REQUIREMENTS Masters or PhD in Bioanalytical Chemistry, Pharmaceutical Science, or related field; Strong project management, compliance, communication, and people skills; Hands on experi...
Medpace, a rapidly growing global Contract Research Organization headquartered in Cincinnati, is seeking a Bioanalytical Quality Assurance (QA) Auditor to join our global QA team. The QA Auditor will play an essential role in ensuring that Medpace upholds a standard for excellence at our various sites and global headquarters by providing accurate, consistent and reliable regulatory guidance. This...
The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivaled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our suc...
Senior Clinical Research Associate (CRA)- join our growing team Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work. An up-front bonus of up $10,000 is possible for CRAs hired with at least 1.5 years of CRA experience; $5,000 as an advance on...
Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work. An up-front bonus of up $10,000 is possible for CRAs hired with at least 1.5 years of CRA experience; $5,000 as an advance on the travel bonus after completion of the training period (4 wee...
Medpace Clinical Operations activities are growing rapidly, and we are currently seeking Directors of Clinical Operations to join our global Clinical Operations team in our Global Headquarters in Cincinnati. Unlike other CROs, our structure allows the clinical trial management team to focus on operational execution of the project, with minimal involvement in P/L of project. This position will prov...
The Project Assistant plays a key role in the Clinical Safety reporting process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Working onsite at Medpace global headquarters in Cincinnati, Ohio the Project Assistant is an integral part of the drug development team. DESCRIPTION...
DESCRIPTION OF JOB DUTIES Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; and Create and maintain project timelines. QUALIFICATIONS/REQUIREMENTS Bachelor's degree in a health sciences field; Prior experience as a Study Coordinator or within the pharmaceutical industry; and Excellent computer (word-processing, databases, Excel,...
Medpace Clinical Operations activities are growing rapidly, and we are currently seeking an Executive level leader to join our global Clinical Operations team in our Global Headquarters in Cincinnati. Unlike other CROs, our structure allows the clinical trial management team to focus on operational execution of the project, with minimal involvement in P/L of project. This position will report dire...
CLINICAL TRIAL MANAGER Medpace is a global, full-service clinical research organization with therapeutic specialization in oncology, cardiovascular, endocrine/metabolic, Infectious disease and CNS. We have steadily expanded operations in nearly forty countries. Headquarters are located in Cincinnati, Ohio with other US offices in Dallas, Texas and Minneapolis, Minnesota. Our clinical operations ac...
DESCRIPTION OF JOB DUTIES Coordinate and conduct internal system audits and external investigative site/vendor audits; Create, maintain, and revise departmental standard operating procedures, forms, and templates; Host audits by sponsors and regulatory inspectors; Coordinate, conduct, and track company-wide regulatory training (ICH/GCP and medical device); Assist QA Director with departmental over...
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