Clinical Research Assistant
Behavioral Health Market Context
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Benefits
The expected salary range for this role is $19.00 - $33.00 USD per hour for full time team membersBenefits & Perks (US Full Time Employees)Paid Time Off (PTO) and Company Paid Holidays100% Employer paid medical, dental, and vision insurance plan optionsHealth Savings Account and Flexible Spending AccountsBi-weekly HSA employer contributionCompany paid Short-Term Disability and Long-Term Disability401(k) Retirement Plan, with Company Match5 more items(s)
Qualifications
- •Bilingual in Spanish required
- •Ability and willingness to work independently with minimal supervision
- •Ability to learn to work in a fast-paced environment
- •Excellent communication skills and a high degree of professionalism with all types of people
- •Excellent organizational skills with strong attention to detail
- •A working knowledge of medical and research terminology
- •A working knowledge of federal regulations, Good Clinical Practices (GCP)
- •Critical thinker and problem solver
- •Friendly, outgoing personality with the ability to maintain a positive attitude under pressure
- •Contribute to team and site goals
- •Proficiency in Microsoft Office Suite
- •High level of self-motivation and energy
- •An optimistic, "can do" attitude
- •A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist
- •Phlebotomy Experience and Proficiency Required
- •California based roles require National phlebotomy certification by an organization approved by the California Department of Public Health
- •Louisiana based roles require National phlebotomy certification by an organization approved by the Louisiana State Board of Medical Examiners
- •Washington based roles require National phlebotomy certification by an organization approved by the Washington State Department of Health
- •Nevada based roles require Laboratory Assistant certification by the Division of Public and Behavioral Health
- •Physical demands associated with this position Include: The ability to use keyboards and other computer equipment
- •17 more items(s)
Responsibilities
- •The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator
- •Ability to understand and follow institutional SOPs
- •Participate in recruitment and pre-screening events (may be at another location)
- •Assist with preparation of outreach materials
- •Identify potential participants by reviewing medical records, study charts and subject database
- •Assist with recruitment of new participants by conducting phone screenings
- •Request medical records of potential and current research participants
- •Schedule visits with participants, contact with reminders
- •Obtain informed consent per Care Access Research SOP, under the direction of the CRC
- •Complete visit procedures as required by protocol, under the direction of the CRC
- •Collect, process and ship specimens as directed by protocol, under the direction of the CRC
- •Record data legibly and enter in real time on paper or e-source documents
- •Request study participant payments
- •Update all applicable internal trackers and online recruitment systems
- •Assist with query resolution
- •Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc
- •Assist with maintaining all site logs
- •Assist with inventory and ordering equipment and supplies
- •Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials
- •Maintain effective relationships with study participants and other care Access Research personnel
- •Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management
- •Communicate clearly verbally and in writing
- •Perform other duties as assigned
- •Location: This is an on-site position with regional commute requirements
- •Regularly planned travel within the region will be required as part of the role
- •Overnight travel will be minimal (<10%)
- •23 more items(s)
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