Regional Clinical Research Associate (CRA): Home Based - Growth Potential / Strong Medical Benefits

Regional Clinical Research Associate (CRA): Home Based – Growth Potential / Strong Medical Benefits

 

 Company DetailsStrong medical benefits 401K & matching programHome office setup includes: laptop, printer, scanner, fax, cell, DSL line, home office line, internet card for travel)Strong therapeutic pipelineGrowth potential – visible environment Efficient reporting structure

 

Position Responsibilities Facilitating and supervising the conduct of clinical trial investigative sites to ensure study protocol compliance in accordance with GCP/ICH guidelinesSupport project management with study activitiesLiaise with Sponsors to track study progress and milestones, regulate quality standardsProvide consistent and ongoing communication with the clinical site and study team throughout the duration of the studyAbility to 60-75% - REGIONAL

 Qualifications Bachelors degree, preferably in the life sciences and/or nursing Minimum of 3 years direct field monitoring experience with a CRO or PHARMA companyStrong knowledge of regulatory and clinical practices (GCP) Demonstrated aptitude and knowledge in more than one therapeutic areaExperience conducting pre-study visits, site initiations, interim monitoring visits and close-out visits

 Desirable TraitsProfessionalExceptional communication skillsCardiovascular experience 

 

 

We appreciate your interest in submitting your credentials for the above opportunity.  Please note, as a professional search firm we will only be responding to those inquiries that most closely align with our clients’ stated requirements.

 

Please include the position title in the subject line of your email to ensure immediate consideration and forward your resume/CV (Word format), in confidence, to: lisa.pagano@wilmingtongroup.com .