What are the responsibilities and job description for the Clinical Research Coordinator position at Headlands Research?
Overview
Peninsula Research Associates (PRA) is dedicated to improving medical treatments through the use of innovative techniques and awareness. PRA strives to educate patients on a vast array of health-related issues with the goal of enriching the quality of life and creating the potential for new opportunities.
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.
Want to be a part of a growing company that’s making a difference in our world? Look no further than PRA! 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 medical, dental, and vision insurance coverage plans
- 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, please apply.
The Role
PRA is looking for a Clinical Research Coordinator who has previous experience coordinating a variety of studies for clinical trials. Under the supervision of the Site Director, the 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.
Position Type: Full-Time
Pay Range: $27.00 - 30.00/hr
Location: Rolling Hills Estates (no remote work)
Work Schedule: Monday- Friday 8:00am - 5:30pm
Responsibilities
- In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
- Manage 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
- Provide the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clients
Qualifications
- Bachelor's Degree preferred
- At least one full year of experience coordinating clinical trials phases 1-4 required
- Nursing license, medical assistant certificate, or similar certification is preferred
- 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
Salary : $27 - $30
