Do you want to watch clinical development change, or do you want to be the one to shape it?
Because we’re hoping you’re here for the latter.
Who are we?
We Are PRA.
We are 15,000+ employees strong, operating in more than 80 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 are getting lifesaving drugs into the hands those who need them most.
Who are you?
You are a Medical Writer who researches, writes, and edits clinical documents by applying functional expertise and clinical drug development knowledge.
Applies a wide range of therapeutic expertise and clinical drug development knowledge to the development of drugs, biologics, devices and/or other products for human use in developing individual clinical study protocols, clinical plan outlines, drug development programs, clinical study reports, manuscripts, investigator brochures, and sections of regulatory submission documents. Also provides therapeutic training to external clients and internal PRA staff.
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.