Clinical Research Coordinator I

ALLIANCE CLINICAL LLC; Los Angeles (CA); On-site; USD 34,000 - 44,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401k

PTO

and more!

Job summary

Alliance Clinical Network is seeking a Clinical Research Coordinator I to support clinical trials at our West Hills and Canoga Park sites. The role covers coordinating visits, data capture, and regulatory compliance with GCP guidelines, while ensuring participant safety and protocol fidelity.

The Coordinator will conduct health assessments, obtain informed consent, manage IP documentation, and assist with site start-up and monitoring activities in a fast-paced setting.

Qualifications

• Requires CPT license and 2+ years phlebotomy/EKG experience.
• Associate degree or equivalent in healthcare or related field.
• Minimum 2 years in healthcare setting; knowledge of FDA regulations and GCP.

Responsibilities

• Coordinate study visits and data collection per protocol.
• Maintain regulatory files and conduct source data verification.
• Obtain informed consent and ensure participant safety and privacy.
• Assist with adverse event reporting and safety monitoring.
• Support study startup, timelines, and collaboration with the PI.

Skills

Phlebotomy

EKG procedures

Attention to detail

Communication

Education

Associate's degree in healthcare or related field

CPT license (Certified Phlebotomy Technician)

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Coordinator I

FullTime Technical West Hills, West Hills, CA, US

Salary Range: $25.00 To $32.00 Hourly

Summary:

The Clinical Research Coordinator I (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants including monitoring the health of each participant throughout the trial. The CRC plays a key part in maintaining study integrity and quality and collaborating with the Principal Investigator (PI) to provide oversight of the study to ensure adherence to Good Clinical Practice (GCP) guidelines.

Essential Duties and Responsibilities:

• Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
• Adhere to site standard operating procedures (SOPs).
• Administer questionnaires and monitor participant compliance with study protocols.
• Respond to participant needs promptly and appropriately.
• Collect and document patient medical history and health conditions.
• Obtain and document informed consent from study participants.
• Maintain accurate records of investigational product (IP) dispensation and accountability.
• Coordinate with laboratories to ensure timely testing and reporting.
• Collect and document information on concomitant medications.
• Review medical records for protocol compliance.
• Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
• Review clinical laboratory reports in accordance with protocol requirements.
• Maintain up-to-date regulatory files for the research site.
• Verify the accuracy and completeness of collected data.
• Monitor and document temperatures for IP storage.
• Support recruitment and engagement of study participants as needed.
• Develop electronic source (eSource) documents in accordance with study protocols.
• Manage study startup documentation, training, and timelines for assigned protocols.
• Ensure all protocol requirements and deadlines are met consistently.
• Maintain strict confidentiality and compliance with regulatory standards.
• Assist with preparation for monitoring visits.
• Enter data into electronic data capture (EDC) systems and resolve data queries.
• Perform other duties as assigned.

Qualifications:

• Minimum of 2 years of experience with phlebotomy and EKG procedures, with a current Certified Phlebotomy Technician (CPT) license required.
• Associate's degree in healthcare or a related field, or equivalent relevant experience.
• Minimum of 2 years of experience in a healthcare setting.
• Minimum of 2 years of experience with FDA regulations and Good Clinical Practice (GCP).
• Demonstrated analytical reasoning skills.
• Exceptional attention to detail and strong organizational skills.
• Excellent verbal and written communication abilities.
• Proven customer service skills with both internal and external stakeholders.
• Ability to effectively manage multiple priorities in a fast-paced environment.

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H-1B, TN, or STEM OPT training plans) are not eligible for this role.

Location: Monday - Friday. On-site at clinics in West Hills, CA and Canoga Park, CA.

Benefits:

• Medical
• Dental
• Vision
• 401k
• PTO
• and more!

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.