ActalentVerified Source

Clinical Research Coordinator Actalent

62K–83K
Onsite · Los Angeles, California
Posted August 12, 2026
payroll

Overview

Lead primary contact with participants sponsors and regulators. Own full lifecycle of studies from initiation to closeout. Drive eligibility determination and consent collection per protocol. Develop recruitment strategies. Oversee specimen collection and data management. Maintain project databases create flow sheets and finalize case reports. Ensure protocol compliance audit case reports and prepare regulatory submissions. Manage IRB renewals assemble study kits monitor procedure scheduling and attend sponsor meetings. Control expenditures and resolve billing issues with finance teams. Collaborate with PI to guarantee patient safety and study integrity. Document all patient and research data appropriately. Oncology Pre-screening patients Chart review Clinical trial Crc Recruitment Edc Patient recruitment

What You'll Do11

  • 1Build recruitment strategies to attract qualified study participants.
  • 2Design and execute study procedures while adhering to budget constraints.
  • 3Ship and monitor study deliverables including specimens and lab data.
  • 4Develop flow sheets and finalize case report forms for accurate documentation.
  • 5Conduct chart reviews and pre-screen patients for trial eligibility.
  • 6Coordinate monitoring meetings with sponsors and principal investigators.
  • 7Maintain compliance with research protocols and audit case reports for accuracy.
  • 8Prepare regulatory submissions and verify IRB renewal status.
  • 9Manage study budgets and resolve billing discrepancies with finance staff.
  • 10Ensure proper filing of patient data in accordance with institutional regulations.
  • 11Track enrollment metrics and provide regular updates to stakeholders.

Requirements11

  • 15+ years building ETL pipelines with Spark and Airflow
  • 23-5 seasons leading clinical research initiatives
  • 3On-site work in Los Alamitos CA
  • 4Medical, dental & vision coverage available
  • 5Critical Illness, Accident, and Hospital insurance optional
  • 6401(k) retirement plan with pre-tax and Roth options
  • 7Life Insurance for employee and dependents
  • 8Disability coverage provided
  • 9HSA participation eligible
  • 10Transportation benefits offered
  • 11Employee Assistance Program available

Salary Insight

$62 - $83k per year

Location

Typeonsite
LocationLos Angeles, California

Required Skills

Clinical researchOncologyPre-screening patientsChart reviewClinical trialCRCRecruitmentEDCPatient recruitmentOncology treatment trials
Share:

Similar open positions

Explore active roles that match your skills and interests.

Actalent

11h agoNew York, New Yorkpayroll

Sr Clinical Research Coordinator Oncology Actalent

Leadership role overseeing clinical trial execution for oncology studies. Manage full lifecycle of trials while collaborating with physicians and research teams. Seeking proactive professional to drive innovative therapies.

73K–87K
Good Clinical Practice (GCP)FDA regulationsIRB processes+8 more

Actalent

11h agoNew York, New Yorkpayroll

Sr 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.

73K–87K
Good Clinical Practice (GCP)FDA regulationsIRB processes+7 more

Actalent

11h agoChicago, Illinoiscontract

Research Coordinator Actalent Chicago

Research Coordinator at Actalent in Chicago leads participant recruitment and data management for clinical trials. This role drives efficient study execution while ensuring regulatory compliance and high-quality data handling.

25K–30K
Clinical research coordinationParticipant recruitmentData entry+7 more
System One

System One

14h agoLos Angeles, Californiacontract

Clinical 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.

26K–30K
electronic data capture systemsclinical trial management softwareMicrosoft Office+2 more

Insight Global

5h agoPhiladelphia, Pennsylvaniapayroll

Clinical Research Coordinator Insight Global

We seek a dedicated Clinical Research Coordinator to lead oncology trials in Philadelphia offering hybrid flexibility. This full-time day shift role requires a bachelor's degree and three years of experience. Join our dynamic team to advance medical knowledge through rigorous research practices.

60K–73K
Clinical trial managementRegulatory complianceHIPAA privacy standards+5 more

Cancer and Blood Specialty Clinic

12d agoLos Angeles, Californiapayroll

Clinical Research Coordinator Oncology Blood Specialty Clinic Los Angeles

The Cancer and Blood Specialty Clinic seeks a Clinical Research Coordinator to lead research efforts across Orange and LA County. This full-time role involves managing clinical studies, recruiting participants, monitoring trials, and collaborating with investigators. Candidates must excel in compliance, communication, and problem-solving to drive impactful research outcomes.

62K–89K
Clinical research coordinationParticipant recruitmentGood Clinical Practice (GCP)+6 more