Regional CRA

Chiltern International is one of the foremost and fastest growing Clinical Research Organizations in North America and Europe. Due to our rapid expansion, Chiltern is seeking highly motivated individuals to join us as an in house CRA in Berwyn PA or throughout the US in a home-based capacity.

The qualified candidate will have a Bachelors degree in a life science or a related field. In addition, we require a minimum of two years monitoring experience as a CRA in a pharmaceutical, biotech or CRO environment. Exposure to Ophthalmology is a plus!

Essential job functions include: Write Protocols, produce CRFs, identify investigator sites, organize investigator meetings, maintain site files, trial master files and study documentation, prepare and conduct initiation visits, conduct monitoring visits and close out visits, work in time lines and within budget restrictions, track clinical trial supplies, track patient recruitment, produce status reports, track SAEs, conduct study close-out activities, work within SOPs, conduct query resolution, and all other duties associated with monitoring and managing clinical trials.

Required skills and abilities include: Good oral and written communication skills, good clinical knowledge with an understanding of medical terminology, good computer literacy, experience working in a team environment, good understanding of the principles of ICH GCP and FDA regulations.

Chiltern's unique corporate culture encourages a healthy balance of personal life and work. We offer an excellent salary and benefits package to include medical & dental, company matching 401K, excellent vacation & holiday and employee incentives. If you have the experience required and feel you are the dynamic person we are looking for, please forward your resume in a Word document via email to tammy.mackenzie@chiltern.com