Clinical Research Coordinator

Nira Medical Group; Salt Lake City (UT); On-site; USD 65,000 - 83,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Job summary

Rocky Mountain Multiple Sclerosis Clinic is seeking an experienced Clinical Research Coordinator to manage Neurology studies. Responsibilities include data entry, scheduling, chart preparation, conducting rating scales, collecting vital signs, blood draws, and ECGs.

The successful candidate will ensure protocol compliance, maintain trial documentation, and communicate with physicians, subjects, and sponsors throughout the study lifecycle. A minimum of 2 years CRC experience is expected.

Qualifications

• Minimum 2 years of clinical research coordinator experience.
• Highly detail-oriented with strong organizational and prioritization skills.
• Excellent verbal and written communication; able to work in a fast-paced environment.

Responsibilities

• Manage Neurology clinical research trials with emphasis on data integrity and regulatory compliance.
• Act as primary contact for study subjects and sponsors; communicate daily as needed.
• Prepare source documents, binders, and study materials; review protocols and brochures.
• Coordinate sponsor visits and oversee sponsor databases.
• Assist with study procedures (pre-screening, screening, visits, vital signs, ECGs, phlebotomy, specimen processing).
• Document patient progress and dose modifications; report adverse events as required.
• Coordinate monitor visits and ensure regulatory documentation is up to date.

Skills

Clinical Research Coordinator

Tools

EMR

Job description

Overview

Rocky Mountain Multiple Sclerosis Clinic is seeking an experienced Clinical Research Coordinator (CRC) to manage Neurology studies. Responsibilities include, but are not limited to EDC data entry, scheduling, chart preparation, conducting rating scales, collecting vital signs, blood draws, and ECGs.

Key Duties

• Responsible for the integrity and overall quality of assigned clinical research trials
• Serves as the primary contact for study subjects and sponsors, communicating daily as needed.
• Reviews study protocols and brochures; creates study document binder and prepares source documents including study and subject information folders.
• Attend sponsor meeting as needed for assigned protocols.
• Oversee sponsor database process.
• Completes study procedures including pre-screening, screening, and study visits in conjunction with Physician/Investigator (may include vital signs, performing EKGs, phlebotomy, processing specimens and shipping to labs).
• Documentation of patient progress in response to investigative agents.
• Coordination of monitor visits with patients.
• Completion of source documents and case report forms.
• Oversee preparation of physician orders to ensure protocol compliance as needed.
• Maintain communication with physician regarding study requirements, dose modifications, and adverse events.
• Upkeeps all trial regulator documentation.
• Maintain high level of understanding of the ICH/GCP guidelines.
• Perform other related duties as assigned.

Qualifications

• A minimum of 2 year's relevant work experience as a Clinical Research Coordinator.
• This person must be highly detailed oriented, possess stellar organizational and prioritization skills, have excellent verbal and written communication and can work in a fast paced environment under limited supervision.
• Skilled with Electronic Medical Record (EMR)

Preferred

• At least 2 years of experience as a Clinical Research Coordinator or similar role; Neurology experience a strong plus. CCRC certified a strong plus.
• Prior working knowledge of research methodology, medical terminology and pharmacology.

What We Offer

• Full Time, 40 hour, Monday to Friday work week.
• Competitive Salary with generous paid time off.
• Medical, Dental, and Vision Insurance.