Clinical Research Coordinator — Interventional Trials

ACTalent; Palo Alto (CA); Hybrid; USD 41,000 - 51,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Short and long-term disability

Paid time off

Job summary

Actalent is seeking a Clinical Research Coordinator in Palo Alto, CA to support interventional drug trials under a principal investigator. The role involves data collection, regulatory documentation, and direct interaction with participants.

You will help ensure protocol compliance, manage study materials, and coordinate activities from start-up through closeout. The position requires at least a two-year degree and one year of CRC experience, with on-site and hybrid work options.

Qualifications

• Two-year college degree and one year of relevant experience in clinical research.
• Experience with interventional drug studies in a clinical research setting.
• Ability to collect, manage, and enter patient and laboratory data for clinical research projects.
• Certifications or active progress toward certification(s) for basic patient measurements such as phlebotomy and EKG.

Responsibilities

• Coordinate studies from start-up through closeout under supervision.
• Serve as a primary contact for participants, sponsors, and regulatory agencies.
• Schedule visits and contact participants with reminders or study requirements.
• Review medical records and collect clinical and demographic data as needed.
• Prepare, distribute, and process study questionnaires and tests.
• Ensure compliance with research protocols and regulatory requirements.

Skills

Clinical study coordination

Regulatory documentation

Data collection and entry

Phlebotomy and EKG training

Interventional drug studies experience

Participant interaction

Education

Two-year college degree

Job description

Actalent is seeking a Clinical Research Coordinator in Palo Alto, CA to support interventional drug trials under a principal investigator. The role involves data collection, regulatory documentation, and direct interaction with participants.

You will help ensure protocol compliance, manage study materials, and coordinate activities from start-up through closeout. The position requires at least a two-year degree and one year of CRC experience, with on-site and hybrid work options.