Clinical Research Coordinator

Duke Careers•Durham, NC

3d•$59,829 - $99,960•Onsite

About The Position

The Department of Surgery is looking for a Clinical Research Coordinator to join our team. This critical role will participate in the day-to-day operations of clinical research for the Cardiovascular and Thoracic Division. The Surgery Office of Clinical Research (SOCR) is staffed with experienced individuals who are dedicated to patient safety while conducting innovative research with the hope of advancing medicine and improving clinical care.

Requirements

Completion of an Associate’s Degree
A minimum of two years of relevant research experience.
A Bachelor’s degree may substitute for two years required experience.

Nice To Haves

Can easily use computing software and web based applications (e.g., Microsoft Office products and internet browsers).

Responsibilities

Applies knowledge to assist with study documentation, protocol submissions, and standard operating procedures (SOPs).
Is responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking, and provision to research participants.
Prepares for and provides support for study monitoring and audit visits, including support for the reviewer. Addresses and corrects findings.
Identifies all AEs, and determines whether or not they are reportable. Collaborates with the PI to determine AE attributes, including relatedness to study.
Conducts and documents consent for participants for all types of studies, including those that are greater than minimal risk or complex in nature and/or require any orders in Maestro Care.
Enters and collects research data. Develops research data entry or collection tools. May provide oversight or training to study team members collecting or entering research data. Ensures accuracy and completeness of data for all studies, including those that are greater than minimal risk or complex in nature.
Prepares for, coordinates, and actively participates in site visits. Communicates effectively with sponsors and/or CROs.
Uses clinical research management system and its reports to manage research participants' activities, calendars, tracking/marking of financial milestones, and all aspects of study visits.
Uses required EHR functionalities to manage participants and study visits.
Proactively seeks opportunities to add relevant skills and certifications to own portfolio.
Keeps current with research updates by attending key external offerings (i.e. Research Wednesday, RPN, events outside of Duke, etc.) and applies the learned material to the job.