Clinical Research Coordinator (2024-0831)

Job Title: Clinical Research Coordinator

Req: 2024-0831

Location: VMC Main Campus

Department: Clinical Research Study

Shift: Days

Type: Full Time

FTE: 1

Hours: M-F, 0800-1600

City State: Renton, WA

Category Professional

Salary Range: Min $67,361 - Max $97,674/annually DOE

Job Description:

VALLEY MEDICAL CENTER

Job Description

(Unit/Clinic/Department Name)

TITLE: Clinical Research Coordinator

JOB OVERVIEW: Clinical Research Coordinators manage clinical studies and site personnel from pre-study planning to successful completion.

ROLE: Clinical support

AREA OF ASSIGNMENT: Valley Medical Center Clinical Research Center

RESPONSIBLE TO: Manager - Valley Medical Center Clinical Research Center

Prerequisites:

Four year degree preferred, national certification a plus.

Phlebotomy License preferred

Qualifications:

Minimum 2 years of experience in a clinical research environment.

Must have a working knowledge and be skilled in the use of personal computers, information storage and retrieval systems.

Candidates must be highly organized, utilize excellent verbal and written communication and able to multi-task

Performance Responsibilities

UNIQUE PHYSICAL/MENTAL DEMANDS, ENVIRONMENT, AND WORKING CONDITIONS:

• Generic Job Functions:
  
  

Clinical Research Coordinator responsibilities include but are not limited to:

Participates in evaluation of new protocols. Maintains/updates all SOP's and supporting procedures.

Pre-screening, screening, recruiting and enrolling patients. Scheduling and retaining patients.

Administer diagnostic tests as required by sponsor protocol.

Data collection and documentation. Collecting and recording adverse events and concomitant medications. Processing Serious Adverse Events. Study drug administration and accountability. All data entry, whether electronic data capture or on paper. Schedule monitor visits, meet with monitors, etc,

Develops and maintains a system for processing/tracking/filing all protocol-related regulatory documentation and study contracts/budgets.

Attend investigator meetings

Source document development

Prepares/completes/complies all forms and documentation for IRB and sponsor submissions, annual reviews, amendments and study closure.

Tracking/submission/filing of all safety reports/adverse events/protocol deviations to sponsors/CROs/IRBs.

Fulfill all reporting obligations to sponsors and CROs

Ensures center activities are in compliance with federal regulations, Good Clinical Practice guideline and center policies.

Management of all miscellaneous tasks involved with coordinating clinical trials

Obtain IATA certification

• Unique Job Functions:
  
  

Conducts in-service/ training for center staff as needed.

Performs Other Related Job Duties As Required.

Revised 1/02, 1,08, 1/09, 2/10

Grade: NC07

Qualifications:

Job Qualifications:

Minimum 1 year of experience in a clinical research environment.

Must have a working knowledge and be skilled in the use of personal computers, information storage and retrieval systems.

Candidates must be highly organized, utilize excellent verbal and written communication and able to multi-task