Instagram
youtube
Facebook

Crc Ii -Research Coordinator

3+ years
$35 to $45 per hour
10 Feb. 15, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

CRC II - Research Coordinator
Matrix Clinical Research
Location: Los Angeles, CA, USA
Employment Type: Full-Time
Compensation: $35 to $45 per hour

Job Summary:

We are seeking a motivated and detail-oriented Research Coordinator to join our team. The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies.

Responsibilities:

  • Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
  • Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data.
  • Attend all relevant study meetings.
  • Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
  • Recruit and screen patients for clinical trials and maintain subject screening logs.
  • Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits.
  • Design and maintain source documentation based on protocol requirements.
  • Schedule and execute study visits and perform study procedures.
  • Collect, record, and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy, and completeness.
  • Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics.
  • Monitor subject safety and report adverse reactions to appropriate medical personnel.
  • Correspond with research subjects and troubleshoot study-related questions or issues.
  • Participate in meetings to confirm daily study tasks are assigned to team members and are executed to the expected standards.
  • Assist with study data quality checking and query resolution.

Qualifications:

  • Must have 3 years of experience as a coordinator.
  • Spanish-speaking / Bilingual preferred.