Senior Clinical Research Coordinator

Want to be a part of a growing company that’s making a difference in our world? Look no further than Artemis Institute for Clinical Research! You’ll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:

• A range of PPO and HMO medical plans
• PPO and HMO dental plans
• Vision coverage, Long Term Disability Plan, and Life/AD&D coverage
• 401k plan
• Paid holidays and paid time off
• A welcoming work environment

We’re looking for a bright, talented new team member to be a part of our story. Check out this current opening and if you think you may be a fit for the role, see instructions for how to apply below.

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.

Position Overview:

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

Company Name: Artemis Institute for Clinical Research

Title of Position: Sr. Clinical Research Coordinator

Position Type: Full Time

Pay Range: $72,800 - $83,000 annually

Location: Riverside - no remote work

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

Required Education and Experience:

• Minimum education: Bachelors Degree Preferred
• Minimum two years of experience as a Clinical Research Coordinator
• Nursing License, Medical Assistant Certificate or similar certification is preferred

Description of Responsibilities:

• 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

Skills/Competencies:

• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremally 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

How to Apply: Follow this link https://hire.jobscore.com/careers/artemisinstituteforclinicalresearch/jobs/clinical-research-coordinator-riverside-bNTEo268Sr6BYlaKjNoogA?previewing=true and click “Apply for this job”

Our Core Values:

1. We always put patients first
2. We deliver the best customer experience every day
3. We do the right thing
4. We work as a team
5. We embrace a journey of continuous improvement