Clinical Research Coordinator

This is a temp-to-hire opportunity located in Fountain Valley, CA. The position is fully onsite, Monday through Friday.

About the role

We are seeking an experienced Consulting Clinical Research Coordinator to join our healthcare team. This role involves managing and overseeing clinical trials in Gynecologic Oncology (GynOnc), ensuring compliance with ethical standards and regulations. You will contribute to groundbreaking research with the potential to significantly impact patient care and treatment outcomes.

Responsibilities

• Oversee the day-to-day management of clinical trials, including 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 Gynecologic Oncology.

Requirements

• 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.
• Proficient in using clinical trial management systems and other related software.
• Detail-oriented with strong problem-solving skills.
• Proven ability to maintain confidentiality and handle sensitive information with discretion.
• Willingness to stay updated on advancements in GynOnc and commitment to improving patient care through clinical research.
• Fluency in English and Spanish.

Skills

• Excellent communication and interpersonal skills.
• Ability to work effectively in a team and independently.

Benefits

• Medical, dental, and vision insurance.
• 401K with company match.
• Paid time off (PTO).
• Sick leave.

Pay

$70,000 - $75,000 per year.