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Job Details

Bridge: Entry Level CRA Oncology Southeast

Company name
Research Pharmaceutical Services, Inc.

Location
Nashville, TN, United States

Employment Type
Full-Time

Industry
Healthcare, Entry Level, Pharmaceutical

Posted on
May 07,2019

Valid Through
Aug 20,2019

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Profile

Overview
Who are you? 
 
You are dedicated to clinical research and have a passion for oncology clinical trials. You thrive in a busy environment, multi-tasking between patient engagement, data entry and regulatory responsibilities required with oncology clinical trials.  You want to help improve lives and you are dedicated to detailed, quality clinical trial work.  Often known as the go to person, you understand the intricacies of oncology clinical trials and are hands on in all facets of an oncology clinical trial.  You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here.  Most of all, you want to do it in a place where you\u2019re more than an employee number. A place you love working.
Responsibilities
What is Bridge? 
 
PRA hires experienced oncology clinical trial coordinator/study coordinators or clinical research nurses and marries that oncology expertise with our exceptional CRA training program to become an oncology CRA monitor. Bridge hires will attend an intensive two week, instructor-led training course in our Corporate office in Raleigh, NC. Our highly-trained CRA mentors provide on-the-job training, working closely and meeting weekly with the new CRAs.
 
What will you be Doing?
 
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Qualifications
What do you need to have? 

Preferred undergraduate degree or its international equivalent in clinical, science or health related field from an accredited institution required OR a licensed healthcare professional (ie, Registered Nurse)
3 years of Study Coordinator or Clinical Research Nurse with hands on ONCOLOGY CLINICAL TRIAL experience required
Must be able to travel up to 80% weekly
60 mins from major international airport
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

Company info

Research Pharmaceutical Services, Inc.
Website : http://www.rpsweb.com

Company Profile
In 1998, RPS began building the foundation for the PRO model in anticipation of evolving clinical strategies within Sponsor companies. By integrating our personnel and systems with those of Sponsor companies, RPS has helped industry leaders achieve significant cost savings, flexible program staffing, and standardized system operations on a global scale. By combining the largest clinical trial recruitment engines with true clinical management oversight, RPS has achieved a service level that is well above the capabilities of any CRO or staffing company in this industry. RPS has had substantial growth and comprehensive development of all the internal infrastructure and systems required to bring the PRO model to full fruition for the benefit of Sponsors.

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