Clinical Research Coordinator

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

Benefits offered by this job

Medical, Dental and Vision Insurance

401K with Match

Temp to Hire

PTO

Sick PTO

Job summary

Jobot Consulting seeks an experienced Clinical Research Coordinator to join our healthcare team in Fountain Valley, CA. This temp-to-hire role focuses on managing gynecologic oncology trials, ensuring regulatory compliance and patient safety.

The ideal candidate has a Bachelor's degree and 3+ years in clinical research, with proficiency in trial management systems. Onsite work Mon-Fri; Spanish and English fluency is a plus.

Qualifications

• 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.

Responsibilities

• Oversee the day-to-day management of clinical trials, including patient recruitment, data collection, and data analysis.
• Ensure all trials are conducted per protocol, ethical standards, and regulatory requirements.
• Coordinate with physicians, nurses, and other healthcare professionals to ensure patient safety and data integrity.
• Develop and maintain relationships with study sponsors, investigators, and stakeholders.
• Prepare and submit regular progress reports on clinical trials.

Skills

Clinical research coordination

GynOnc knowledge

Regulatory knowledge

Communication

Data analysis

Teamwork

Confidentiality

Education

Bachelor's degree

Tools

CTMS

Data collection software

Job description

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

Job details:

This Jobot Consulting Job is hosted by: Ba Tran

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

Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions.

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