Clinical Research Coordinator: Patient-Driven Trials

Actalent; Orange (CA); On-site; USD 52,000 - 55,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance (Voluntary)

Transportation benefits

PTO / Vacation & Sick Leave

Job summary

Actalent is seeking a Clinical Research Coordinator to oversee day-to-day operations of multiple clinical studies at Orange, CA sites. You will serve as a primary liaison among the Principal Investigator, patients, sponsors, and IRB, ensuring GCP/ICH compliance and meticulous study documentation.

The role emphasizes patient interaction, IP handling, data entry, and coordination of visits, labs, and regulatory filings in a fast-paced clinical environment.

Qualifications

• Minimum of 2 years in a clinical research setting with patient-facing responsibilities.
• Informed consent, vitals, EKGs, labs, and medication dispensing experience preferred.
• Ability to read and follow regulatory guidelines (GCP/ICH).
• Strong documentation, organization, and communication skills.

Responsibilities

• Oversee daily operations of multiple clinical research studies under supervision.
• Serve as primary contact for investigators, patients, sponsors, and monitors.
• Manage IP accountability, inventory, temperature and expiration monitoring.
• Enter visit data into EDC systems within defined timelines.

Skills

EPIC EMR

Outlook

MS Teams

Excel

Data entry

Tools

EPIC EMR

Job description

Actalent is seeking a Clinical Research Coordinator to oversee day-to-day operations of multiple clinical studies at Orange, CA sites. You will serve as a primary liaison among the Principal Investigator, patients, sponsors, and IRB, ensuring GCP/ICH compliance and meticulous study documentation.

The role emphasizes patient interaction, IP handling, data entry, and coordination of visits, labs, and regulatory filings in a fast-paced clinical environment.