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 16,000+ employees strong, operating in more than 85 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.
Who are you?
You are someone who wants to be part of a fabulous group; a group that really supports their folks and promotes from within! Science, Clinical Trials and Data are your passion, and you want to be a part of drug research and development, then this is for you! You also enjoy tracking clinical studies and being a part of the big picure!
Still here? Good. Because if this is you, Late Phase Services would love to meet you!
What will you be doing?
As a Site Management Associate, you will perform investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, in-house site management, and data review activities in accordance with the study protocol, client and/or PRA standard operating procedures (SOPs), and all applicable guidelines and regulatory requirements (e.g. ICH-GCP, and country/region specific).
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.