Who are we?
We Are PRA.
We are 15,000+ 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 known to friends and colleagues alike as the “go-to” person. You have excellent communication & follow-up skills. With your commitment to executing projects in accordance with the highest standards, you hold a certain reverence for the regulatory processes, SOPs and document trails that map out a pathway to compliance. But most of all, you are someone with tremendous potential who wants to apply your many talents in a role that will expand your fundamental knowledge of clinical research and provide you with the options and training to continue to grow in your career.
What will you be doing?
As a Clinical Trials Specialist, you are the primary point of contact/liaison for the sites, Sponsor and internal stakeholders during the study life cycle. You will perform investigative site recruitment/feasibility, essential document collection and review, maintenance and close-out in-house site management activities in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP guidelines and all applicable regulatory requirements. In addition, you will create and distribute meeting agendas and take meeting minutes during internal and Sponsor calls, roll out training plan to team members, and provide access to project systems. Senior-level IHCRAs will manage all activities listed above, ensure that they meet Sponsor & PRA expectations, and deliver them in accordance with the contract, trial protocol, ICH/GCP and applicable SOPs.
What do you need to have?
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities.