Clinical Research Coordinator

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

Clinical Research Coordinator

Fountain Valley,CA, US

Experience: Mid Level

Salary: $70,000 - $75,000 per year

Job Details

• Bachelor's degree in a related field preferred
• 3+ years of experience in clinical research coordination
• Prior experience in Gynecologic Oncology (GynOnc) is a plus!
• Excellent knowledge of clinical trial design, management, and regulatory requirements
• Strong understanding of Good Clinical Practice (GCP) guidelines
• Exceptional organizational skills and ability to manage multiple clinical trials simultaneously
• Excellent communication and interpersonal skills
• Proficient in using clinical trial management systems and other related software
• Ability to work effectively in a team and independently
• Detail-oriented with strong problem-solving skills
• Proven ability to maintain confidentiality and handle sensitive information with discretion
• Willingness to stay updated on the latest trends, developments, and advancements in the field of GynOnc
• Commitment to improving patient care and treatment outcomes through clinical research
• NOTE: We are fully onsite (M-F) at our Fountain Valley, CA location; hybrid not available

What will you be doing?

• Oversee the day-to-day management of clinical trials, including but not limited to, patient recruitment, data collection, and data analysis
• Ensure all clinical trials are conducted in accordance with the study protocol, ethical standards, and regulatory requirements
• Coordinate with physicians, nurses, and other healthcare professionals to ensure patient safety and the integrity of clinical trial data
• Develop and maintain effective relationships with study sponsors, investigators, and other key stakeholders
• Prepare and submit regular reports on the progress and results of clinical trials
• Participate in the development of study protocols, informed consent forms, and case report forms
• Identify, evaluate, and manage potential risks and issues related to clinical trials
• Provide training and guidance to other members of the clinical research team
• Stay updated on the latest trends, developments, and advancements in the field of GynOnc

A bit about us:

We are seeking an experienced Consulting Clinical Research Coordinator to join our healthcare team. This is an exciting opportunity to be part of a team that is at the forefront of clinical research in the healthcare industry. You will play a crucial role in managing and overseeing clinical trials, ensuring they are conducted in accordance with ethical standards and regulations. You will be directly involved in groundbreaking research that has the potential to significantly impact patient care and treatment outcomes in the field of Gynecologic Oncology (GynOnc). This position requires fluency in English and Spanish.

Why join us?

• Medical , Dental and Vision Insurance
• 401K w/ Match
• Temp to Hire opportunity
• PTO
• Sick PTO
• and more!