Clinical Research Coordinator (Crc)

1-2 years

$25 - $35 per hour

Los Angeles

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

Clinical Research Coordinator (CRC)

Company: Advancing Research International

Location: Los Angeles, CA, USA

Employment Type: Full-Time

Salary: $25 - $35 per hour (based on experience and qualifications)

Benefits: Medical, Paid Time Off

About Us:

Advancing Research International is an ophthalmology-specific Site Management Organization (SMO) conducting Phase I-IV FDA-regulated clinical trials. Headquartered in Los Angeles, CA, we operate satellite sites in Las Vegas, San Francisco, and Phoenix.

Position Overview:

We are seeking a highly organized and detail-oriented Clinical Research Coordinator (CRC) to join our team. The CRC will manage clinical research studies across our network, ensuring compliance with regulatory requirements, ethical guidelines, and study protocols. This is an in-house position, requiring direct collaboration with sites across our network.

Bilingual English/Spanish is required.

Key Responsibilities:

Coordinate and oversee all aspects of clinical research studies, including participant recruitment, enrollment, and retention.
Assist in regulatory submissions, including IRB applications and informed consent documentation.
Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and study protocols.
Conduct study visits, perform patient assessments, and collect accurate data.
Maintain up-to-date case report forms (CRFs) and essential study documents.
Serve as a liaison between Principal Investigators (PIs), sponsors, and research teams.
Document and report adverse events (AEs) and serious adverse events (SAEs) per protocol.
Support site initiation, monitoring visits, and close-out activities.
Coordinate lab tests, imaging studies, and other trial-related procedures.
Train and mentor new research staff as needed.
Address study-related queries from participants, research teams, and sponsors.

Qualifications:

Required:

1-2 years of experience as a Clinical Research Coordinator or Clinical Research Assistant (preferably in an in-house setting).
Knowledge of ICH-GCP, FDA regulations, and clinical trial operations.
Strong communication and organizational skills.
Ability to manage multiple tasks and prioritize effectively.
Proficiency in Microsoft Office Suite and clinical trial management software (e.g., Medidata).
Ability to work both independently and collaboratively.
Bilingual (English/Spanish).

Preferred:

Phlebotomy skills or certification.
GCP and International Air Transport Association (IATA) certification.
Experience with electronic data capture (EDC) systems.

Compensation & Benefits:

Hourly Pay: $25 - $35 per hour (commensurate with experience)
Paid Time Off (PTO)
Health Insurance
Professional Development Opportunities

Working Conditions:

In-office role with occasional travel to network sites.

Company Address: 4036 Whittier Blvd, Los Angeles, CA 90023

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