CRA II

Clinical Research Associates have a career that enables you to contribute directly to the development of new therapies that impact millions of lives around the globe.  We seek people who are passionate about improving the quality of human life through scientific research.  Our CRAs partner with investigative sites to ensure applicable guidelines for human safety and ethics are being followed, data is accurate, and study procedures are being followed. 

We are a multi-national top five clinical research organization.  You will join a team of strong professionals and a management team dedicated to your career development.  Some of our best people grew into key leaders in the company.  We are a company of 12,500 employees in forty countries globally.  We differentiate ourselves by developing innovative solutions to bring life-saving drugs to market faster and in a more cost-effective way to foster better patient outcomes.  We are a top five clinical research organization with solid earnings and growth potential.  Our belief in excellence is our core value in all that we do for our sponsor partners and the patients that we serve.  As a company we strive to exceed our customers’ expectations in drug development solutions. 

We care about our people, since they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term careers.  Caring for patients while enjoying what we do and delivering great results is something we can achieve if we know we can count on each other and have a clear vision of where we want to go.

Foremost, you will also be an expert in the study protocol to ensure it is being adhered to, that data is clean and accurate, and that trial participants are consenting and being treated in an ethical manner.  You will carefully review medical records; visually inspect storage and handling of investigative products and supplies; communicate questions, concerns, and discuss findings with the clinical staff and investigators; identify obstacles and solutions for overcoming them; and discuss corrective actions when issues arise.  You will at all times stay in close contact with your sites about their progress.  Additionally you will ensure that all regulatory filings are current.  You’ll ensure that the trial is operating according to guidelines like ICH/GCP, that it is complying with laws and regulations, and that standard operating procedures are being followed. 

We’re seeking CRAs who see their role as beyond mere fact checking.   We are looking for monitors who can spot trends and underlying concerns for the best possible outcomes.  Our CRAs don’t sit on the sidelines.  They are active participants in the well-being and management of their clinical sites.  We are looking for people who enjoy that no two days will be alike. 

We look for people with experience in site monitoring who can read and interpret medical records, review findings, and who have a deep understanding of local and international laws and guidelines for the conduct of clinical trials. 

We invite you apply to our clinical research associate opportunities for Phases II - IV.  We are seeking experienced CRAs with a desire to travel.  A bachelor’s degree in the life sciences preferably will ensure your familiarity with regulatory guidelines and clinical terminology.  A minimum two years of site monitoring experience will ensure your success on our team.  You will need to be a legal resident of the country to which you apply as well as have authority to work without sponsorship.  The ability to speak fluently and write in English is required.