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PRAHS Clinical Trial Assistant - Blue Bell PA in United States

We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.

Who are we?

We Are PRA.

We are 16,000+ employees strong, operating in more than 90+ countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most.

What will you be doing?

You will be responsible for setting up, tracking and maintaining Clinical Site related documents. You will help manage and review regulatory documents as well as maintain the Local Study File. Assist with coordinating the distribution, retrieval and review of regulatory documents required for the initiation of the Clinical Study, through maintainence, and close-out.

Performs the role of Clinical Trial Assistant (CTA) supporting the Local Trial Manager and Site Manager to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials. Performs regulatory document review and approval, including site specific Informed Consents. Ensures trial related activities are in compliance with GCO SOPs, policies and local regulatory requirements. May contribute to process improvement, training and mentoring of other CTA’s.

  • Demonstrated expertise and experience in the Clinical Trial Coordination

  • Ability to maintain Clinical Trial Tracking systems.

  • Exhibits proficiency in managing multiple projects and deliverables with competing priorities.

  • Bachelor’s Degree preferred in scientific/medical discipline or equivalent experience.

  • Read write and speak fluent English

  • Familiarity with working in service industry or project management environment.

What do you need to have?

  • 2 years of related experience

  • Experience with study start-up, maintanance, close-out of clinical studies

  • Prior experience using computerized information systems.

  • Read, write, and speak fluent English; fluent in host country language required

  • Experience with clinical trials required

  • 4 yr degree highly preferred or equivalent industry experience

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.

ID: 2019-55284

External Company Name: Pharmaceutical Research Associates, Inc

External Company URL: