Medical Assistants/Licensed Practical Nurses/Registered Nurses
Lufkin, TXFull-time
Behavioral Health Market Context
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Qualifications
- •Seeking clinically experienced candidates who bring strong patient care skills, professionalism, and attention to detail
- •Prior clinical research experience is not required
- •Experience as a Medical Assistant (MA), Licensed Practical Nurse (LPN), or Licensed Vocational Nurse (LVN)
- •Active CMA or LPN/LVN license, where applicable
- •Experience performing EKGs/ECGs
- •Strong patient care and communication skills
- •Experience documenting in an EMR or similar clinical system
- •Strong organizational skills, attention to detail, and ability to manage multiple priorities
- •Professionalism, reliability, accountability, and willingness to learn
- •Interest in developing into a clinical research career path
- •7 more items(s)
Responsibilities
- •The MA/LPN/RN will work under the direction of the clinical Principal Investigator (PI) on multiple ongoing research studies
- •This role provides hands-on training in clinical research operations, patient-facing study procedures, research documentation, protocol execution, and compliance expectations
- •Assist with patient flow for clinical research visits and protocol-specific activities
- •Prepare patients for visits, procedures, and follow-up requirements
- •Obtain vital signs and perform clinical tasks within scope and training
- •Obtain informed consent visits and reinforce patient education under supervision
- •Perform EKGs/ECGs, phlebotomy, specimen collection, and other protocol-related procedures as permitted by license and training
- •Prepare rooms, equipment, and study materials for patient visits
- •Coordinate visit scheduling across multiple active studies
- •Document study visits accurately, thoroughly, and in real time
- •Maintain complete, organized, and audit-ready source documentation
- •Enter study-related data into sponsor systems, EDC platforms, and internal tracking tools
- •Support day-to-day study operations and visit logistics
- •Liaise with investigators, coordinators, nurses, and site staff to keep study visits on track
- •Track study supplies, lab kits, equipment, and visit materials
- •Communicate professionally with internal teams, sponsors, CROs, vendors, and monitors as appropriate
- •Identify and escalate issues that may affect patient safety, protocol compliance, or study quality
- •Complete required study, sponsor, and site training assignments
- •Learn and follow protocol requirements, GCP standards, site SOPs, and applicable regulatory expectations
- •Willingness to travel up to 25% as needed
- •17 more items(s)
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