Headlands Research
Clinical Research Coordinator I
Headlands Research, San Diego, California, United States, 92189
Overview
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.
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 plansPPO and HMO dental plansVision coverage, long term disability plan, and life/AD&D coverage401k planPaid holidays and paid time offA welcoming work environmentWe'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, please apply.
The Role
Artemis is looking for a Clinical Research Coordinator I for the San Diego office. Under the supervision of the Site Director, the Clinical Research Coordinator I 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 I manages study conduct from planning through study closeout.
Position Type:
Full Time
Pay Range
:
$27-$30/hr
Location:
San Diego-no remote work
Travel:
10%
Work Schedule:
Monday & Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm
Responsibilities
In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent qualityManaging 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 MeetingsProviding the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clientsQualifications
Bachelor's Degree preferredMinimum one year experience as a Clinical Research Coordinator requiredNursing license, medical assistant certificate, or similar certification is preferredCommitment and ability to deliver excellent customer serviceExcellent communication, punctual and responsibleExtremely well organizedExcellent verbal and written communication skillsTrustworthy, reliable; attentive to detailsMature and pleasant demeanorWillingness to learn new tasks and grow with the company
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.
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 plansPPO and HMO dental plansVision coverage, long term disability plan, and life/AD&D coverage401k planPaid holidays and paid time offA welcoming work environmentWe'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, please apply.
The Role
Artemis is looking for a Clinical Research Coordinator I for the San Diego office. Under the supervision of the Site Director, the Clinical Research Coordinator I 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 I manages study conduct from planning through study closeout.
Position Type:
Full Time
Pay Range
:
$27-$30/hr
Location:
San Diego-no remote work
Travel:
10%
Work Schedule:
Monday & Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm
Responsibilities
In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent qualityManaging 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 MeetingsProviding the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clientsQualifications
Bachelor's Degree preferredMinimum one year experience as a Clinical Research Coordinator requiredNursing license, medical assistant certificate, or similar certification is preferredCommitment and ability to deliver excellent customer serviceExcellent communication, punctual and responsibleExtremely well organizedExcellent verbal and written communication skillsTrustworthy, reliable; attentive to detailsMature and pleasant demeanorWillingness to learn new tasks and grow with the company