Coordinate all aspects of patient involvement in clinical trials while adhering to ICH, GCP, and company guidelines. Perform safety and efficacy assessments, document adverse events, and manage regulatory duties to ensure study compliance.
Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials.
Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country.
Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability.
We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
$29.00/hr - $34.00/hr ( depending on education, experience, and skillset )
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
1.
Indoor, Office environment.
2.
Shift work, depending on location.
3.
Essential physical requirements include sitting, typing, standing, and walking.
4.
Lightly active position, occasional lifting of up to 20 pounds.
Rarely lift over 20 pounds.
5.
Reporting to work, as scheduled, is essential.
6.
Overnight travel may be required for training and/or investigative meetings.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Requires a high school diploma (Bachelor's preferred) and at least one year of experience as a Clinical Research Coordinator. Candidates must have a strong understanding of federal regulations protecting human subjects and effective communication skills.
Market context
Clinical Research Coordinator roles in California are often driven by active hospital, academic, and sponsor-led studies, so candidates with human-subjects compliance knowledge and coordinator experience tend to stay competitive. This posting’s requirements and benefits are AI-summarized from the original job description, helping you review the role faster; the summary shows a high school diploma with a bachelor’s preferred, plus at least one year of CRC experience, and benefits including health, dental, vision, STD, and LTD. Before applying, compare your experience with federal research regulations and be ready to describe how you manage participant communication and study documentation.
