Onsite Clinical Research Coordinator GynOnc Trials

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

Benefits offered by this job

Medical, Dental and Vision Insurance

401K w/ Match

Temp to Hire opportunity

PTO

Sick PTO

Job summary

LeoForce in Fountain Valley, CA is seeking a Clinical Research Coordinator to manage day-to-day clinical trials, focusing on Gynecologic Oncology. This onsite role requires a Bachelor's degree and 3+ years in clinical research, with bilingual English/Spanish preferred.

You will coordinate with physicians and study teams, ensure compliance with GCP and study protocols, and handle data collection, reports, and regulatory documentation.

Qualifications

• Bachelor's degree in a related field preferred.
• 3+ years of experience in clinical research coordination.
• GynOnc experience is a plus.
• Strong knowledge of GCP and regulatory requirements.
• Proficient with clinical trial management systems.
• Excellent organizational and communication skills.
• Fluency in English and Spanish.

Responsibilities

• Oversee day-to-day management of clinical trials, including patient recruitment, data collection and analysis.
• Ensure trials comply with study protocols, ethics and regulatory requirements.
• Coordinate with physicians, nurses and healthcare staff to ensure patient safety and data integrity.
• Prepare reports and communicate progress to sponsors and investigators.
• Develop study protocols, consent forms and case report forms.
• Maintain confidentiality and handle sensitive information.

Skills

Clinical trial design

GCP guidelines

Data management

Regulatory compliance

Communication

Team collaboration

Multilingual: English/Spanish

Education

Bachelor's degree

Tools

CTMS

Electronic data capture

EMR/EHR systems

Job description

LeoForce in Fountain Valley, CA is seeking a Clinical Research Coordinator to manage day-to-day clinical trials, focusing on Gynecologic Oncology. This onsite role requires a Bachelor's degree and 3+ years in clinical research, with bilingual English/Spanish preferred.

You will coordinate with physicians and study teams, ensure compliance with GCP and study protocols, and handle data collection, reports, and regulatory documentation.