Clinical Research Coordinator

Clinical Research Coordinator | Temp to Hire | $$$$

This Jobot Consulting Job is hosted by: Ba Tran
Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume.
Salary: $70,000 - $75,000 per year

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!

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

Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.

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