Are you looking to make a big impact?

Artemis is seeking an experienced Clinical Research Coordinator (Senior/III) to make a big impact at our clinical research site located in Riverside, CA.  Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Senior Clinical Research Coordinator supervises a team of research assistants and a lab tech, is heavily involved in training and mentoring other clinical research coordinators and direct reports, and serves as the Site Director's right hand woman/man.

Position Type:  Full Time, 40 hours per week

Travel Required:  0%; Onsite required

Pay Range:  $76,000-$90,000/yr (based on years of exp as a CRC)

Location:  Riverside, CA

Work Schedule: Monday- Friday 7am-4:00pm

About Artemis Riverside & Headlands Research

Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials.

Together with Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

• In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
• Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending investigator meetings
• Experience managing multiple studies as the primary coordinator and someone ready to take the next step in managing people
  • Will supervise a team of research assistants and a lab tech
  • Involved in mentoring and training the other RAs and CRCs to optimize their engagement and performance
• Interested in leadership opportunities or career growth
• Providing the highest level of care for study patients and delivering excellent customer service to the pharmaceutical clients

• Bachelor's Degree preferred
• Minimum of 3 years of experience delegated as the lead Clinical Research Coordinator on multiple studies at once required 
• Nursing license, medical assistant certificate, or similar certification is preferred
• Phlebotomy skills or willingness to become phlebotomy trained required
• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremely well organized with a high level of attention to detail
• Excellent verbal and written communication skills
• Trustworthy & reliable
• Mature and pleasant demeanor
• Willingness to learn new tasks and grow with the company