Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Home-Based anywhere in the United States

You will:

Conduct and report all types of onsite monitoring visitsBe involved in study startup (if applicable)Perform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team in preparing documents for study submissions

QualificationsCollege/University degree in Life Sciences or an equivalent combination of education, training & experienceExperience as a Study Coordinator (or similar role) is requiredExperience working on Gastroenterology clinical trials required Full working proficiency in EnglishPC skills to be able to work with MS Word, Excel and PowerPointAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility and willingness to travel frequently Valid driver’s license

Additional Information

Become a full-fledged clinical research professional with the support of a knowledgeable and professional team.  You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.