Clinical Research Coordinator - 119425

Medix™; Los Angeles (CA); On-site; USD 60,000 - 85,000; Full time

Job summary

Medix in Los Angeles is seeking a Clinical Research Coordinator to ensure the integrity and quality of clinical trials. You will be the primary contact for subjects and sponsors, coordinate study visits, pre-screenings and documentation, and support sponsor meetings.

The role requires attention to detail, strong organizational skills, and the ability to work in a fast-paced environment under limited supervision.

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)

Responsibilities

• Maintain integrity and quality of assigned clinical research trials.
• Serve as primary contact for study subjects and sponsors, communicating daily as needed.
• Review study protocols and brochures; create study binder and prepare source documents including study and subject information folders.
• Attend sponsor meetings as needed for assigned protocols.
• Execute study procedures including pre-screening, screening, and visits with Physician/Investigator (may include vital signs, EKGs, phlebotomy, processing specimens and shipping to labs).
• Document patient progress in response to investigative agents.
• Coordinate monitor visits with patients.
• Complete source documents and case report forms.
• Oversee preparation of physician orders to ensure protocol compliance.
• Maintain communication with physician regarding study requirements, dose modifications, and adverse events.
• Upkeep all trial regulator documentation.
• Maintain high level of understanding of the ICH/GCP guidelines.
• Perform other related duties as assigned

Skills

Detail oriented

Organizational skills

Verbal and written communication

Tools

EMR

Job description

Estimated Duration of Assignment: ~12 month contract (subject to change based on company needs/requirements - this means that it could wrap up early and/or be extended)

Responsibilities

Key duties include but not limited to:

• 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.
• Completes study procedures including:
• Pre-screening, screening, and study visits in conjunction with Physician/Investigator (may include vital signs, performing EKG's, 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.)