Job Description
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 18 sites across the US and Canada, with plans for further expansion.
Want to be a part of a growing company thats making a difference in our world? Look no further than PRA! Youll 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
Were 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 Research Assistant who has previous experience coordinating a variety of studies for clinical trials. Under the supervision of the Site Operations Manager, the Research Assistant will be responsible for supporting various activities associated with the day-to-day operations of the research department in the
conduct of clinical trials.
Position Type: Full Time
Pay Range : $18.00 - 22.00/hour
Location: Rolling Hills Estates, CA (no remote work)
Work Schedule: Monday- Friday 8:00am - 5:30pm
Responsibilities:
- Collect, process, and assist in the compilation and verification of research data, samples, and/or
specimens (following strict protocol and detailed instructions) - Become familiar with Research Standard Operating Procedures and study protocols
- Collect clinical data with patient contact for diary compliance or routine surveillance calls
- Enter data from forms and documents into databases and other documents
- Collect, process (potentially including PBMCs if site deems qualified to train), and ship
blood/urine specimens at scheduled patient visits - Complete and maintain case report forms per FDA guidelines, and review them against the
patients medical record for completeness and accuracy - Maintain study specific logs, including Pre-screening, enrollment, consent, lab processing logs
- Assist coordinators with creation of source documents and preparation of kits and binders
- Collect vital signs and assist with electrocardiograms
- Phlebotomy (if qualified)
- Provide general office support to keep operations running smoothly
- Prepare and Summarize progress reports and project results
- Ensure compliance with FDA, Sponsor, Good Clinical Practice (GCP) guidelines
Qualifications:
- Clinical Research experience preferred
- Healthcare experience in a direct patient-facing role preferred
- Bachelors Degree in related field preferred
- Interpersonal and communication skills interact effectively with professional, administrative
staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources. - Knowledge in medical terminology and laboratory skills a plus
- Accuracy, attention to detail and ability to independently set priorities and meet deadlines
- Excellent communication, punctual and responsible
- Extremely well organized
- Excellent verbal and written communication skills
- Trustworthy and reliable
- Mature and pleasant demeanor
- Willingness to learn new tasks and grow with the company
Job Tags
Holiday work, Full time, Remote job, Monday to Friday,