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CLINICAL PROTOCOL COORDINATOR

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Job Details
Job Order Number
JC171301639
Company Name
Loyola University Chicago
Physical Address

Chicago, IL 60684
Job Description

CLINICAL PROTOCOL COORDINATOR
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Position Details

Job Title
CLINICAL PROTOCOL COORDINATOR

Position Number
8150114

Job Category
University Staff

Job Type
Full-Time

FLSA Status
Non-Exempt

Campus
Maywood-Health Sciences Campus

Department Name
ONCOLOGY INSTITUTE

Location Code
ONCOLOGY INSTITUTE (06310A)

Is this split and/or fully grant funded?
No

Duties and Responsibilities

• Processes local IRB submissions to include new research projects, amendments, adverse events and study terminations.
• Processes FDA submissions Establish and maintain research project’s regulatory files.\
• Ongoing communication with the local IRB, federal organizations, affiliate institutions and pharmaceutical study sponsors.
• Ongoing communication within the research team regarding research project changes.
• Collects, records and maintains accurate data reporting adhering to protocol data collection protocol and federal guidelines.
• Clarifies Data Queries.
• Coordinates with the Clinical Research RN to organize procurement of research samples and then prepares, packages and ships research samples.
• Manages research sample supplies.
• Participates in Cooperative Group Audits, NCI, FDA, Sponsor GCP quality audits, Loyola internal audits and department audits.
• Performs related duties as assigned.

Minimum Education and/or Work Experience

Minimum Education:
Required: Bachelor’s Degree OR equivalent training acquired via work experience or education
Preferred: Bachelor’s Degree
Specify Degree(s): Bachelor of Science

Minimum Experience:
Required: Less than one year of previous job-related experience
Preferred: 1-2 years of previous job-related experience
Details: Clinical trials experience

Qualifications

• Ability to follow oral and written instructions and established procedures.
• Ability to perform basic filing, office procedures and word processing.
• Ability to maintain accuracy and consistency.
• Ability to communicate verbally.
• Ability to finish tasks in a timely manner.
• Ability to maintain confidentiality.
• Ability to compose letters and memorandums.
• Ability to deal calmly and courteously with people.
• Ability to analyze and interpret data.
• Ability to function independently and manage own time and work tasks.
• Ability to work as an effective team member.
• Ability to organize workflow.
• Ability to negotiate, persuade and establish direction.
• Ability to maintain office files and follow standard office procedures.
• Skilled job requiring high level of adaptability & interpersonal skills.
• Ability to interact with internal and external constituents.

Certificates/Credentials/Licenses

CCRA (Certified Clinical Research Associate) or equivalent (SoCRA or ACRP)

Computer Skills

• Proficiency with Microsoft Word, Groupwise, EPIC, Microsoft Excel, Basic Keyboarding Skills, Adobe Acrobat, Beacon.
• Clinical Trials Management System.
• Electronic data entry web based data bases.

Supervisory Responsibilities
No

Required operation of university owned vehicles
No

Does this position require direct animal or patient contact?
No

Physical Demands
None

Working Conditions
None

Open Date
06/23/2020

Close Date

Special Instructions to Applicants

Quick Link for Posting
http://www.careers.luc.edu/postings/14004


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