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Assistant Clinical Research Coordinator

Company: Covance
Location: Madison
Posted on: January 18, 2020

Job Description:

Job Overview: Overall accountability for the operational conduct of assigned studies, working closely with the Project Manager, Principal Investigator and operational staff and ensuring that all studies are conducted in accordance with regulatory and protocol requirements, and standard operating procedures whilst maintaining the safety and integrity of the study. The Clinical Research Coordinator is the primary site contact for the Project Manager (PM) communicating any potential issues and assists in taking appropriate action in response to these issues, ensuring that client requirements and timelines are always met or exceeded. Independently undertakes routine studies and more complex studies with guidance. May coach and mentor Operations coordinators and junior staff. Additional Responsibilities: Study Set-up – Performs all aspects of the set up process to include the development and approval of study specific documents, study schedules and clinical procedure planning Coordination - Coordinates the running of critical events, i.e. check in, PK days, check out by resolving/escalating issues identified by both staff and study participants. Monitors and maintains participant safety, dignity and compliance, including coordination of appropriate medical consultation/treatment as appropriate. Provides updates regarding study participants wellbeing to the investigators and Project Manager including adverse event updates Study Meetings -Facilitates/attends and contributes to all key Study Planning meetings, i.e. Clinical Start Up Meeting, Clinical Planning Meeting, Site Initiation Meeting Protocol Review – Reviews protocols, provides consolidated comments from the clinical site on the draft study protocol to the Project Manager or Medical Writer, taking into account the logistics, safety (staff and study participants), and site’s capabilities. May distributes final protocols and amendments to the site Education/Qualifications: Knowledge of protocol designs, study objectives and study procedures Knowledge of drug development process, ICH guidelines and GCP Excellent written and oral communication skills Ability to prioritize workloads Good organizational skills Previous customer service experience desirable Previous experience of coordinating people or processes desirable Experience: University/college degree desirable (life science, pharmacy or related subject preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing certification, medical or laboratory technology). In lieu of a degree, typically 3 years’ experience in a related field will be considered

Keywords: Covance, Madison , Assistant Clinical Research Coordinator, Other , Madison, Wisconsin

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