Clinical Research Coordinator I, Laboratory (Onsite) Angeles Clinic

California Jobs; Los Angeles (CA); On-site; USD 50,000 - 80,000; Full time

Job summary

A leading company based in Los Angeles is seeking a Clinical Research Coordinator I to support clinical research protocols onsite. Your role will involve collaboration with investigators and ensuring compliance with protocol requirements, handling laboratory specimens, and assisting with patient recruitment. The position requires a high school diploma, experience in healthcare or research, and relevant certifications.

Qualifications

• 6 months of healthcare or research experience required.
• Experience as a clinical research coordinator or assistant preferred.
• Must obtain BLS certification within 60 days of hire.

Responsibilities

• Process research laboratory specimens and manage sponsor deliveries.
• Coordinate patient screening and recruitment.
• Document and report data accurately.

Skills

Phlebotomy

Laboratory Skills

Data Management

Communication

Education

High School Diploma/GED

Phlebotomy Certification

Basic Life Support (BLS) certification

Job description

Clinical Research Coordinator I, Laboratory (Onsite) Angeles Clinic

This position supports clinical research protocols within the department. The Clinical Research Coordinator will collaborate with investigators, subjects, staff, and sponsors to ensure protocol compliance and regulatory adherence. The role is 100% onsite, with no remote or hybrid options available.

Primary Responsibilities:

1. Accurately process research laboratory specimens, including centrifugation, aliquoting, storage, and shipment, demonstrating proficiency and adherence to study protocols.
2. Manage deliveries from sponsors, including inventory checks, unpacking, storing supplies, and maintaining electronic records.
3. Handle administrative tasks such as scheduling research visits, maintaining consent and source documents, and documenting adverse events.
4. Support patient screening and recruitment, including explaining trial concepts and assisting with informed consent.
5. Coordinate logistical aspects of research projects, ensuring protocol compliance and patient safety.
6. Collect, document, and report data accurately and timely, responding to sponsor queries as needed.
7. Participate in monitoring and auditing activities to ensure compliance, implementing corrective actions when necessary.
8. Compile and report study data, including protocol activity and accrual information, for research meetings.
9. Work with investigators and IRB to submit adverse events, protocol deviations, and safety reports.
10. Act as liaison with pharmaceutical representatives and funding organizations to monitor project progress.
11. Assist with research-related billing, distinguishing between routine and research care.
12. Attend research meetings, workshops, and seminars as required.

Qualifications:

• High School Diploma/GED required.
• At least 6 months of healthcare or research experience.
• One year of experience as a clinical research coordinator or assistant.
• Phlebotomy and lab assistant experience with demonstrated competency.
• Phlebotomy Certification from California (include license number in resume).
• Basic Life Support (BLS) certification from AHA (must be obtained within 60 days of hire).

Preferred Qualifications:

• Associate Degree or College Diploma preferred.
• Experience in processing research laboratory specimens per protocols.
• Proficiency in managing study supplies and inventory.

This role is strictly onsite; no remote or hybrid arrangements are available.

About the company

Notice

Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Reasonable accommodations are provided for qualified applicants with disabilities. Contact: [e-mail] or 407-000-0000.

All new hires must complete Form I-9 and provide proof of work eligibility. An AEDT scores your application; details at www.talentify.io/bias-audit-report. NYC applicants may request alternative processes at [e-mail] or 407-000-0000.