Clinical Research Coordinator

Clinical Research Coordinator

Location: Northridge, CA (91325)

Pay: $62,400 - $70,000

Hours: On-site, Monday-Friday, 8am-5pm

Format: Direct Hire

• Read, understand, and accomplish protocol-specified patient visits and procedures.
• Clearly and concisely document patient assessments, observations, test results, and other study-related information per federal regulations, protocol requirements, and GCPs.
• Obtain patient informed consent according to federal regulations, GCPs, and IRB requirements.
• Be creative and diligent in recruiting qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsor's timeline while following regulations and rules governing medical ethics, IRB, GCP, and ICH guidelines.
• Complete all required training in a timely manner.
• Schedule and conduct patient visits according to protocol requirements and timelines.
• Maintain accurate and complete written source documentation of patient visits and protocol-related activities.
• Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor.
• Maintain confidentiality of patient and protocol issues as appropriate and as bound by Confidentiality Agreements between company, sponsors, and other entities, as well as HIPAA regulations.
• Promptly report adverse events to supervisor and/or Principal Investigator/Sub-Investigator as deemed necessary.
• Report Serious Adverse Events (SAEs) to sponsor within 24 hours of becoming aware of the SAE. Also report the SAE to the supervisor, Principal Investigator, and/or Sub-Investigator.
• Account for clinical trial materials (i.e., CRFs, study drug, lab supplies, and/or other required items) and ensure availability of appropriate amounts for the conduct of the study.
• Maintain ongoing communication with Team Lead I, Team Manager, Principal Investigator, Sub-Investigators, and other people assisting with the trial, documenting these communications according to protocol requirements and company policies.
• Attend required training courses/conferences to stay abreast of current and changing federal regulations and company policies.
• Pursue educational opportunities to increase knowledge of the research process and associated rules and regulations governing clinical research.
• Attend Investigator Meetings and/or other training as directed.
• Perform all study-related duties in a time- and cost-effective manner in adherence with company policies.
• Perform all duties in a safe and prudent manner.
• Represent the company in a professional and courteous manner (verbal, written, and in appearance) when interacting with staff, sponsors, IRBs, patients/subjects, and nursing and medical staff members of various clinics, hospitals, and physician's offices.
• Perform other duties as assigned.

Required Skills:

• Travel required.
• Exposure to human bodily fluids.
• Laboratory processing procedures.
• Subject/Patient care.
• Daily computer use.
• Occasional night and weekend work schedules.
• Ability to properly lift 35 pounds and occasionally more than 35 pounds.
• Ability to drive, and daily availability of an automobile.


Minimum Requirements:


• Education: Bachelor's degree preferred; however, is not required.
• Experience: Preferably a minimum of 2 years' experience as a CRC, plus 1-3+ years' minimum experience within the field of clinical research or biological research.



For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).

This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.

Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.

Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?