GynOnc Clinical Research Coordinator — Onsite

Leoforce; Fountain Valley (CA); On-site; USD 70,000 - 75,000; Full time

Benefits offered by this job

Medical Insurance

401K Plan

Temp to Hire

PTO

Sick PTO

Job summary

Leoforce is seeking a Clinical Research Coordinator in Fountain Valley, CA to manage gynecologic oncology trials. The role requires coordinating patient recruitment, data collection, and regulatory compliance, collaborating with physicians and study staff.

You will ensure protocol adherence, safety, data integrity, and timely reporting while staying current with evolving GynOnc research. Fluency in English and Spanish is valued.

Qualifications

• Bachelor's degree in a related field preferred.
• 3+ years of experience in clinical research coordination.
• Experience in Gynecologic Oncology (GynOnc) is a plus.
• Strong knowledge of clinical trial design, management, and regulatory requirements.
• Proficient in GCP guidelines and data privacy.

Responsibilities

• Oversee day-to-day management of clinical trials, including recruitment, data collection, and analysis.
• Ensure trials are conducted per protocol, ethics, and regulatory standards.
• Coordinate with physicians, nurses, and healthcare professionals to ensure patient safety and data integrity.
• Maintain relationships with sponsors, investigators, and stakeholders.
• Prepare regular progress and results reports on trials.
• Assist in study protocol development, informed consent, and CRFs.
• Identify and manage risks related to clinical trials and provide team training.

Skills

Regulatory compliance

GCP guidelines

Data collection & analysis

Communication skills

Bilingual English/Spanish

Education

Bachelor's degree in a related field

Tools

Clinical trial management systems

Job description

Leoforce is seeking a Clinical Research Coordinator in Fountain Valley, CA to manage gynecologic oncology trials. The role requires coordinating patient recruitment, data collection, and regulatory compliance, collaborating with physicians and study staff.

You will ensure protocol adherence, safety, data integrity, and timely reporting while staying current with evolving GynOnc research. Fluency in English and Spanish is valued.