Clinical Research Coordinator, Phase I-IV Trials
Overview
Coordinate Phase I-IV clinical trials with strict adherence to ICH and GCP guidelines at CenExel Clinical Research. Manage patient involvement from study initiation through completion across diverse therapeutic areas like Psychiatry, Dermatology, and Neurology. Work onsite in Los Angeles with a dedicated team of research professionals and a collaborative environment that prioritizes quality and work-life balance. This role includes direct patient interaction, data management, and regulatory duties, offering a chance to impact clinical research quality.
What You'll Do10
- 1Coordinate all patient involvement from study initiation to completion, ensuring protocol compliance and safety.
- 2Organize research information for clinical trials, including source documents, case report forms, and study supplies.
- 3Observe subjects and assist with data analysis and reporting, documenting adverse events and protocol deviations per GCP.
- 4Schedule data collection, including vital signs, EKGs, and blood draws, per protocol requirements.
- 5Document adverse events, protocol deviations, and other unanticipated problems appropriately.
- 6Report research data to maintain quality and compliance with federal regulations.
- 7Perform administrative and regulatory duties related to the study, including preparing regulatory submissions.
- 8Participate in protocol development activities and coordinate with sponsors to ensure accurate information and supplies.
- 9Educate potential participants and caregivers on protocol details and expectations.
- 10Perform safety and efficacy assessments per protocol, including vital signs, EKGs, and blood draws.
Requirements9
- 11+ years experience as a Clinical Research Coordinator, required.
- 2High school graduate or equivalent; Bachelor's Degree preferred.
- 3Knowledge of federal regulations protecting human subjects in research and governing clinical trials.
- 4Strong leadership and mentorship skills.
- 5Ability to develop and maintain effective working relationships at all levels of the organization, including sponsors and vendors.
- 6Crisis management and problem-solving skills, with a calm and effective approach in emergent situations.
- 7Ability to work independently and as part of a team.
- 8Effective verbal and written communication skills.
- 9Indoor office environment; shift work may apply; light physical activity with occasional lifting up to 20 pounds.
Salary Insight
$60 - $71k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
System One
VerifiedClinical Research Coordinator, Regulatory Compliance
As a Clinical Research Coordinator, you will own the execution of clinical protocols at our Inglewood site, supporting 5+ active studies with a focus on participant safety and data integrity. You'll work directly with the Principal Investigator and senior research staff, collaborating with cross-functional teams including data management and regulatory affairs. This contract role stands out for its hands-on involvement in the full study lifecycle, from screening to closeout, in a fast-paced research environment.
Actalent
VerifiedSr Clinical Research Coordinator Oncology
Lead senior clinical research coordinator overseeing study execution for diverse portfolio of investigator initiated and industry sponsored trials. Seeking proactive research professional passionate about clinical research patient care and driving innovative therapies.
Research Centers of America
VerifiedData Entry Coordinator - CenExel Clinical Research
The Data Entry Coordinator will own clinical research data entry at CenExel Clinical Research. This role operates under moderate supervision within a team focused on quality people teamwork and optimal work-life balance. Candidates should thrive in a fast paced environment and enjoy collaborative settings.
DocTrials
VerifiedClinical Research Coordinator - DocTrials
Coordinate patient visits and lead interventional protocols at multiple Phoenix Valley offices. Manage patient acquisition and enrollment through community outreach while ensuring strict adherence to FDA and ICH-GCP guidelines. Consolidate study data and communicate updates via Basecamp.
START Center for Cancer Research
VerifiedClinical Research Coordinator at START Center for Cancer Research
Join the START Center for Cancer Research as a Clinical Research Coordinator. You will lead daily activities of early phase oncology clinical trials while supporting senior research staff. This role ensures accurate and timely conduct of clinical research following protocols and regulatory standards.
CenExel Clinical Research
VerifiedMedical Assistant Clinical Research CenExel Clinical Research
CenExel seeks a skilled Medical Assistant to provide direct support to Clinical Research Coordinators while adhering to ICH GCP protocols. This full-time onsite role offers competitive hourly wages between $20.00 and $22.50. The position emphasizes teamwork and expertise in complex early-phase trials.