Study Start up
5 개월전에
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.
Why Medpace?
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Awards:
Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer Recognized by Forbes as one of America's Best Mid-size Companies in 2021 Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility-
Study Start Up Manager
5 개월전에
Seoul, 대한민국 AstraZeneca 풀타임Typical Accountabilities Contribute to ensure that clinical and operational feasibility assessment of potential studies is performed to the highest quality. Accountable for study start-up and regulatory maintenance being in charge with collection, preparation, review and tracking of documents for the application process; Accountable for submission of...
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Site Care Partner
6 개월전에
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Sr. Clinical Trial Manager
5 개월전에
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Clinical Trial Assistance
6 개월전에
Seoul, 대한민국 IQVIA 풀타임Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...
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Site Activation Specialist
5 개월전에
Seoul, 대한민국 IQVIA 풀타임Essential Functions • With moderate oversight and supervision, serve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project...
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Seoul, 대한민국 Novo Nordisk 풀타임Are you passionate about driving strategic initiatives and programs in the field of Real World Evidence (RWE)? If so, we have an exciting opportunity for you to join our Clinical, Medical, Regulatory Affairs (CMR) department as a Real World Evidence Associate. Read on to learn more and apply today for a life-changing career. About the departmentThe...
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Seoul, 대한민국 Novo Nordisk 풀타임Are you passionate about driving strategic initiatives and programs in the field of Real World Evidence (RWE)? If so, we have an exciting opportunity for you to join our Clinical, Medical, Regulatory Affairs (CMR) department as a Real World Evidence Associate. Read on to learn more and apply today for a life-changing career. About the departmentThe...
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Real World Evidence Manager
6 개월전에
Seoul, 대한민국 Novo Nordisk 풀타임Are you passionate about driving strategic initiatives and programs in the field of Real World Evidence (RWE)? Do you have experience in managing teams and engaging with stakeholders? If so, we have an exciting opportunity for you to join our Clinical, Medical, Regulatory Affairs (CMR) department as a Real World Evidence Manager. Read on to learn more and...
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Seoul, 대한민국 Novo Nordisk 풀타임Are you passionate about driving strategic initiatives and programs in the field of Real World Evidence (RWE)? Do you have experience in managing teams and engaging with stakeholders? If so, we have an exciting opportunity for you to join our Clinical, Medical, Regulatory Affairs (CMR) department as a Real World Evidence Manager. Read on to learn more and...
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Assoc Clin Project Mgr
6 개월전에
Seoul, 대한민국 IQVIA 풀타임Job Overview Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with...
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Account Manager
6 개월전에
Seoul, 대한민국 Amazon Web Services Korea LLC 풀타임Would you like to be part of a team focused on increasing adoption of Amazon Web Services by developing Start-up accounts? Do you have the business savvy and the technical background necessary to help establish Amazon as a key technology platform provider?As a Account Manager, you will have the exciting opportunity to help drive the growth and shape the...
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Therapeutic Area Lead
6 개월전에
Seoul, 대한민국 AstraZeneca 풀타임Medical & Scientific engagement for internal and external stakeholders 1. To establish AstraZeneca as a scientific leader through proactive, updated and effective Medical input Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds. Develop and implement the local medical plan to address unmet...
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Seoul, 대한민국 Work Visa USA Jobs (move2usajobs.com LLC) 풀타임Description: Embark on an exciting venture to the United States through our J-1 Governmental Sponsor Program, which provides placements in traineeships and internships across various states for aspiring IT professionals. As an IT Trainee/Intern, you'll be thrust into the forefront of technological innovation, working on projects that span software...
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