Assistant Clinical Research Coordinator I

ZipRecruiter; Los Angeles (CA); On-site; USD 45,000 - 75,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to support clinical trials and contribute to medical innovation. This role involves screening participants, coordinating visits, and maintaining study documentation, all while ensuring compliance with regulatory guidelines. Ideal for those looking to advance their career in clinical research, you'll work in a dynamic environment where your contributions will directly impact patient lives. Join a passionate team dedicated to improving healthcare through groundbreaking research and make a difference in the field of medical science.

Qualifications

• Bachelor’s degree in a health-related field or equivalent experience.
• Certified Phlebotomy Technician (CPT) certification required.

Responsibilities

• Assist in screening and recruiting study participants according to protocol eligibility criteria.
• Collect and record study data accurately in case report forms (CRFs).
• Ensure compliance with study protocols and regulatory requirements.

Skills

Organizational Skills

Communication Skills

Interpersonal Skills

Attention to Detail

Ability to Work Independently

Ability to Work Collaboratively

Education

Bachelor’s degree in a health-related field

Certified Phlebotomy Technician (CPT)

Tools

Microsoft Office (Word, Excel, Outlook)

Electronic Data Capture Systems

Job description

Job Description

JOB LOCATION/SCHEDULE:

Monday – Friday / on-site / Los Angeles

COMPANY OVERVIEW: Alliance Clinical Network we’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day.

SUMMARY: The ACRC will assist in the execution of clinical trials in compliance with study protocols, regulatory guidelines, and Good Clinical Practice (GCP). This position is ideal for individuals looking to grow their career in clinical research and contribute to advancing medical science.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Assist in screening and recruiting study participants according to protocol eligibility criteria.
• Schedule and coordinate participant visits, including study procedures, assessments, and follow-ups.
• Collect and record study data accurately in case report forms (CRFs) and electronic data capture (EDC) systems.
• Maintain study documentation, including source documents, regulatory files, and participant records.
• Support informed consent discussions by ensuring participants understand study requirements.
• Assist in monitoring participants for adverse events and report findings to the CRC or Principal Investigator (PI).
• Coordinate specimen collection, processing, and shipment per protocol requirements.
• Ensure compliance with study protocols, institutional policies, and regulatory requirements (FDA, IRB, ICH-GCP).
• Prepare study materials, including study kits, lab supplies, and regulatory binders.
• Communicate effectively with investigators, study sponsors, monitors, and other research staff.
• Perform administrative duties related to research studies, such as data entry, filing, and appointment reminders.

QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION AND EXPERIENCE:

• Bachelor’s degree in a health-related field (e.g., Biology, Nursing, Public Health, or related discipline). Equivalent experience may be considered.
• Certified Phlebotomy Technician (CPT) certification required.
• Prior experience in healthcare, research, or clinical settings is a plus but not required.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.
• Strong organizational skills and attention to detail.
• Excellent communication and interpersonal skills to interact with patients, staff, and external stakeholders.
• Ability to work both independently and collaboratively in a fast-paced environment.
• Proficiency in Microsoft Office (Word, Excel, Outlook) and ability to learn electronic data capture systems.