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Contracts Associate 1 Study Start-Up Duties Responsible for the commercial relationship with sites involved in clinical trials including work from contract and amendment language budget negotiation within the established timeline..
PRA Health Sciences is a global Contract Research Organisation working in a dynamic and technology driven industry. The people we employ, in over 70 countries, are key to our success...
MEDICAL COPY EDITOR - office based in Northern NJ This position is responsible for ensuring editorial and grammatical accuracy, relevance, consistency and compliance of all materials that go through the..
The Regulatory Affairs Associate (RAA) and is responsible for preparing, submitting and following up on initial and amended Regulatory Agency (RA), Central Independent Ethics Committee (IEC), and any other central..
Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we?..
Calling ALL Experienced Clinical Research Associates – Read On, Join the Movement We believe that our people are the future of the industry. We provide a culture in which our..
This position is characterized by the performance of a variety of administrative and office support duties. Positions require knowledge of company and departmental policies and procedures in order to communicate..
One thing we all have in common is the drive to produce great results for our clients and to advance treatment options available to patients worldwide. We always have a..
SunIRef:itnAssoc Software EngineernJob Locations (All) | US-PA-Blue BellnPosted Date 5 hours ago(9/15/2020 1:07 PM)nIDn2020-67719nOverviewnAssociate Software EngineernnSymphony Health Solutions, a wholly owned subsidiary of PRA Health Sciences, is a leading provider..
Site Contract and Budget Specialist Responsibilities: Ensures the successful negotiation and on-going management of clinical trial agreements with investigative sites. Works cross functionally with Clinical Operations and Project Management in..
EMEA – Home or Office Based Our Study Start Up structure represents an integrated, dedicated, seamless team of experts, all striving to minimize cycle times. This is especially true of..
The In House Clinical Research Associate (IHCRA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance with the Sponsor and/or..
Site Contract And Budget Specialist The candidate will be responsible for the development and analysis of contractual relationships including investigator grants including drafting, negotiating, and finalizing agreements related to clinical..
Job DetailsnFull-timeEstimated: $55,000 - $69,000 a year1 hour agonnBenefitsn- Health insurancennQualificationsn- Clinical trialsn- Clinical researchnnFull Job DescriptionnJob Locations (All) | US-OH-ClevelandnPosted Date 6 hours ago(9/2/2020 12:19 PM)nIDn2020-67260nOverviewnCalling ALL Experienced Clinical..
Contracts Associate 1 (Study Start-Up) Duties: Responsible for the commercial relationship with sites involved in clinical trials including work from contract and amendment language, budget negotiation within the established timeline..
Who are we? We Are PRA. We are 17,000 employees strong, operating in more than 90 countries. We are committed to saving lives and we are constantly striving to be..
At PRA, we don’t make our 16000 people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small..