Job description

Clinical Research Assistant

Works under the direction and supervision of Clinical Research Coordinator (CRC), and Principal Investigators (PI) in the site management of clinical research studies in accordance with the study protocol, guidelines, and site-specific policies and procedures.

Duties and responsibilities include but are not limited to the following:

· Maintains current training in Good Clinical Practice (GCP) and study specific training

· Assists CRC with all study-related activities according to study protocol

· Assists CRC and PI with screening patients to identify potential subjects according to the Inclusion/ Exclusion Criteria

· Obtaining proper informed consent for each potential study patient prior to any study-related activity and provides subject with a copy including emergency contact information

· Prepares source documents and other study materials under the direction of the CRC

· Completion of source documentation at each study visit including scanning, faxing, and
filing activities

· Assists CRC in preparation for monitoring visits and follow up activities with PI

· Maintains study logs including but not limited to subject enrollment, temperature, subject stipend, shipping, and biological sample logs

· Ensures that study supplies such as lab collection kits and investigational drug or devices are received, stored, distributed, and documented according to study protocol

· Ensures proper handling of pathology or lab specimen obtained for study purposes

· Performs study subject activities as required by protocol (e.g., VS, EKG, Lab specimens etc.)

· Completes all required documentation of study visits and follow up visits or phone calls in a timely and accurate manner

· Resolution of queries in a timely manner

· Schedules study visits and maintains the study calendar

· Assists with study closure, return or destruction of study materials, and proper storage of study documents according to SOP and sponsor guidelines

· Attends scheduled conference calls with study sponsors including remote monitoring

· Maintains patient confidentiality of all charts, supplies, and study information

· Additional study-related activities to support success of study

Job Requirements:

· Graduate of an accredited program with current State of Tennessee licensure (MA, LPN, or RN)

· Excellent organizational skills and detail oriented

· Effective oral and written communication skills

· Good computer skills and basic math skills

· Proficient knowledge of medical terminology

· Ability to coordinate activities with other research team members

· This FT position may involve limited local travel to other sites

Job Type: Full-time

Pay: $16.00 - $18.00 per hour

Benefits:

• 401(k) matching
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Education:

• High school or equivalent (Preferred)

License/Certification:

• LPN License (Preferred)
• MA License (Preferred)

Work Location: In person

gatheringourvoice.org is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, gatheringourvoice.org provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, gatheringourvoice.org is the ideal place to find your next job.