Full Job Description
Meditrial is a full-service contract research organization with a successful track record supporting medical device and biotechnology companies in all phases of clinical development. Operating throughout Europe and the United States to manage trials sponsored primarily by US Companies, we offer highest level expertise across multiple therapeutic areas including notable depth in cardiovascular and respiratory, orthopedics, oncology, CNS, infectious disease, endocrinology, diabetes, among other indications. We are passionate about our mission to support the innovation and development of better therapies in healthcare in compliance with solid ethical standards. Our commitment has resulted in excellent results for business growth by creating stability and opportunities for employees and collaborators.
Clinical Research Associate:
Meditrial offers great opportunities for clinical research associates (CRAs), in the United States. We offer attractive income potential, outstanding career progression and exposure to cutting-edge training and technology.
Conducting site initiation, monitoring visits and investigator training
Reviewing study case report forms (CRFs) completed by the investigative sites, and verifying entries by validating accurate source documentation to support CRF entries
Documenting site visits and issues in reports and follow-up letters to the site
Facilitating effective communications among investigative sites, the client and Meditrial
Identifying potential investigators in collaboration with the client
Responding to company, client and national regulatory requirements/audits
Contributing to the project team by assisting in project communications and study submissions
Higher or specialized secondary education degree in natural sciences
Familiar with electronic CRF and CTMS systems
Industry background: CRO/outsourced services, Pharmaceuticals, Biotechnology
Recent experience in medical device clinical trials
Fluency in the English language; knowledge of a second language is a plus