Clinical Research Coordinator - Infectious Disease

Description

Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health's world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.

TheClinical Research Coordinatorplays a key role in the planning, coordination, and execution of clinical research studies-from design and startup through study closeout. This position is responsible for implementing and managing all aspects of research activities for one or more studies, ensuring that projects are completed on time and in compliance with institutional policies, FDA regulations (CFR), and ICH Good Clinical Practice (GCP) guidelines.

The ideal candidate is organized, detail-oriented, and collaborative, with the ability to prioritize multiple projects and meet critical deadlines. In this role, you will work closely with the Principal Investigator (PI), research teams, sponsors, and institutional departments to ensure successful study conduct, financial oversight, and proper support across all phases of research.

This is an excellent opportunity to make a meaningful impact in advancing clinical research and improving patient care.

Salary : $35.31 - $56.82 hourly

10% Limited position, may convert to career

Qualifications

Required :

• Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
• Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
• Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
• Ability to be flexible in handling work delegated by more than one individual.
• Typing and computer skill / ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
• Working knowledge of the clinical research regulatory framework and institutional requirements.
• Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
• Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
• Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
• Ability to interact non-judgmentally with a wide diversity of individuals including drug-using and alternate lifestyles
• Willingness to travel to various office location as needed