Who are we? we are praWe are 20,000+ employees strong, operating in more than 90 countriesWe are committed to saving lives and constantly striving to be the best at what we doOur impact is real, and we see it every dayWe are getting life-saving drugs into the hands of those who need them most. Highlights:
Exciting opportunity to work as part of a dedicated pra team supporting an embedded client, a top global pharmaceutical company Ability to work with cutting-edge clinical technology used by pra and the client Excellent career advancement potential
Cra with 1 to 2+ years of clinical monitoring experience. Territory: midwestern uS(primarily texas)
Monitor the progress of clinical studies (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 Demonstrates excellent knowledge of ich/gcp Displays ability to manage investigative sites to facilitate trial deliverables Escalates issues appropriately, as needed Conducts monitoring to confirm subject safety and data integrity Describes and demonstrates the principals of ip accountability Identifies scientific misconduct at the site level Demonstrates working knowledge of microsoft office applications, clinical trial management systems, ivrs/iwrs and electronic data capture platforms Mentors cras new to the position or company Serves as an observation visit leader Conducts monitoring evaluation visits Assists team lead in the development of trial tools or documents Applies knowledge of pra’s policies and procedures, and demonstrates excellent written and oral communication with all internal / external stakeholders
Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution, a licensed health-care professional (e.g., rn), or equivalent work experience; 1 to 2+ years of clinical monitoring experience Experience in monitoring all trial components (pssv to cov) Knowledge of ich and local regulatory authority regulations regarding drug development. Experience in coaching/mentoring other cras Solid communication skills, including the ability to read, write, and speak fluent english.
Advanced degree (e.g., m.s., m.b.a., pharmd) Therapeutic area experience: experience working in cystic fibrosis and/or other rare diseases.
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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