Regional Clinical Studies Associate (Home-Based)

PRA Health Sciences - Remote3.4

Contract
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Job Locations (All) | US-Remote
Posted Date 3 weeks ago(10/22/2018 2:02 PM)
ID
2018-49845
Overview
As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

At PRA, borders do not create boundaries. PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 15,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.

Responsibilities
Develops/maintains study documents and utilizes company systems to manage clinical biomedical studies. Provides administrative support to project team members in clinical operations and project management. Works with the project team to ensure that projects are completed in accordance with contract and client expectations. Completes project management tasks as assigned by the study project manager/project director. Project management tasks will provide opportunities to broaden exposure to project management activities and to develop core project management skills.

Expert knowledge of applicable systems/processes
Proficiency in using applicable business applications including word processing, spreadsheet, presentation programs
Basic knowledge of basic principles of timeline management, project financials, and risk management
Working knowledge of the company’s industry and service offerings
Understanding of relevant regulations
Familiarity with medical terminology
Read, write and speak fluent English; fluent in host country language
Advanced knowledge of some functional activities based on previous work assignments
Understanding of client contract, scope of work
Qualifications

REQUIRED EXPERIENCE:
3 years’ experience in clinical research in a similar position
Bachelor’s degree or international equivalent in business, finance, health sciences, or related field
Experience with Study Start-up, regulatory documentation collection and quality control

PREFERRED EXPERIENCE:
Experience working with Investigator Initiated Studies - Highly preferred
Experience working within clinical systems, electronic trial master file - preferred

To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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