This job has closed.

University of South Florida · 2 days ago

Clinical Research Coordinator II

Greater Tampa Bay Area

Full-time

Onsite

Entry, Mid Level

2+ years exp

The University of South Florida is a top-ranked research university dedicated to cultivating a talented workforce. The Clinical Research Coordinator II will serve as the main point of contact for sponsors and patients, responsible for managing clinical research projects and ensuring compliance with protocols.

EducationTrainingUniversities

Hiring Manager

Katherine Friborg

Responsibilities

Plans, organizes, and manages the resources necessary to achieve clinical research project goals and objectives at a single site

Coordinates and performs patient clinical assessments for clinical trial visits for assigned clinical trial protocols including scheduling with vendors which may include other departments or outside facilities. This may include phlebotomy, sample processing, vitals, ECGs and other delegated clinical assessments per assigned protocols

Communicates as a site representative with study sponsors, third party vendors, clinical teams and patients to ensure all protocol required elements are being completed and collected within the defined windows

Ensures site compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends site monitoring meetings with sponsors

Manages the site research project databases, develops flowsheets and other study related documents, and completes source documents/case report forms

May provide guidance to other clinical research staff and support personnel

Makes recommendations of procedures in order to facilitate protocol compliance

Performs data entry and query resolution during the duration of each trial assigned

Serve as a resource for both internal and external customers and members of the community in regard to clinical research processes at the site

Performs other duties as assigned

Qualification

Clinical research principlesClinical PracticeRegulatory requirementsData collectionAttention to detailOrganizationTechnical adviceSoftware applicationsCritical thinkingClear communication

Required

Bachelor's degree in a related field -OR- equivalent combination of education and experience

Minimum of two (2) years of related experience

Senate Bill 1310- The Florida Senate is conditional upon meeting all employment eligibility requirements in the U.S

Related work experience may not substitute for any required licensure, certification, or registration required for the position of employment as established by the public employer and indicated in the advertised description of the position of employment

Comprehension of clinical research principles, Good Clinical Practice Guidelines, and regulatory requirements

Attention to detail, critical thinking, ability to follow protocols

Ability to maintain quality standards, planning and scheduling, data collection, clear communication, and organization

Ability to communicate and interact competently and professionally at all levels within a broad, complex clinical research environment

Ability to provide technical advice, guidance, and support to professional and support staff

Skill in the use of personal computers and related software applications

Ability to travel to other USF campuses and/or other locations as requested