Senior Clinical Research Coordinator - 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 18 sites across the US and Canada, with plans for further expansion.

The Role

Artemis is looking for a Senior Clinical Research Coordinator for the Riverside office. 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 manages study conduct from planning through study closeout.

Position Type:  Full Time, 40 hours per week

Travel Required:  0%

Pay Range:  $76,000-$90,000/yr

Location:  Riverside, CA

Work Schedule: Monday- Friday 7am-3:30pm

• 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
• Providing the highest level of care for study patients and delivering excellent customer service to the pharmaceutical clients

• Bachelor's Degree preferred
• 2+ years of experience delegated as the Clinical Research Coordinator on multiple studies at once required 
• Nursing license, medical assistant certificate, or similar certification is preferred
• Previous training or willing to become phlebotomy trained required
• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremely well organized
• Excellent verbal and written communication skills
• Trustworthy, reliable; attentive to details
• Mature and pleasant demeanor
• Willingness to learn new tasks and grow with the company