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Job Details

Sr IRT Validation Tester

Company: Chiltern
Location: Remote from anywhere in the U.S. or Canada
Reference: IRTTester
Closing Date: 23 Mar 18
Type: Full Time
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

We are currently searching for permanent, remote IRT Validation Testers to join our team. In this role, you will ensure that outsourced electronic trial systems (IRT, IVRS, ePRO) implemented in a trial meet or exceed both Chiltern and client expectations.

Requirements:

Job Background

 The IRT Validation Tester should be able to:

  • Implement a logical, risk-based test approach to creating, executing and documenting test plans and test cases
  • Write clear, concise, and thorough test documents; provide peer review on documentation
  • Convert complex technical and business requirements into an understandable test plan and test cases
  • Execute test cases according to defined plans and guidelines
  • Facilitate project testing with internal and external clients; coordinate efforts with multiple testers
  • Ensure timeliness of all project/client deliverables

 

REQUIREMENTS

  • 4-year degree in computer science, life science, engineering, business, or related field
  • 3+ years’ experience in a quality assurance, business analysis, clinical research or data management environment
  • Experience with clinical systems, such as RTMS, CTMS, ePRO, IVRS, EDC, Oracle Clinical or related technology 
  • Knowledge of SDLC, GCP, and FDA regulations
  • Knowledge of Drug Development and Clinical Trials Processes, and the Software Development Lifecycle associated with clinical trials
  • Excellent communication, organization, and time management skills, as well as strong attention to detail and ability to manage multiple projects simultaneously

 

At Chiltern, you’ll join a team of like-minded individuals headed by some of the most dynamic and influential leaders in drug and medical device development today. You’ll work on cutting-edge global research projects in a fast-paced but collegial atmosphere where you’ll have the opportunity to make meaningful — and acknowledged — contributions. You’ll have opportunities to grow personally and professionally and abundant room for advancement along with generous incentive programs.

Chiltern. is a leading midsized provider of comprehensive clinical research and development services with offices in more than 30 countries and a customer base comprised of some of the world's top pharmaceutical, biotech and medical device companies. As a forerunner in medical device and drug-device combination trials with notable capabilities in pharmaceuticals and biologics, Chiltern offers deep expertise in a broad range of therapeutic areas and in all phases of development. With some of the industry's top scientists and most advanced clinical analytics capabilities, Chiltern ensures smooth-running, successful trials. For the full-service, right-size global research partner, don't think twice. THINK CHILTERN.

Chiltern is an equal opportunity employer, M/F/D/V

Salary

Negotiable

Position Type

Permanent
Full Time

Contact

Email Jim Doyle - James.Doyle@Chiltern.com
+1 484 679 2497

Apply for this job: Sr IRT Validation Tester

Contact Information:

Address:  Pennsylvania, USA
1016 W 9th Ave, King of Prussia, United States
PA 19406
USA
Website:  Visit Our Web Site

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