Registered Nurses

SiteBridge Research•Lufkin, TX

13d•Onsite

About The Position

SiteBridge Research Inc: Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry-sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. The SiteBridge Network extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes. Job Description: Medical Assistants/Licensed Practical Nurses/Registered Nurses We are seeking Medical Assistants (MAs), Licensed Practical Nurses (LPNs), or Registered Nurses (RNs) who want to transition into clinical research. Seeking clinically experienced candidates who bring strong patient care skills, professionalism, and attention to detail. Prior clinical research experience is not required. The MA/LPN/RN will work under the direction of the clinical Principal Investigator (PI) on multiple ongoing research studies. Candidates with experience in cardiology, cardiovascular medicine, internal medicine, or other specialty outpatient settings are strongly preferred. Experience with EKGs/ECGs and phlebotomy is highly desirable. This role provides hands-on training in clinical research operations, patient-facing study procedures, research documentation, protocol execution, and compliance expectations. The position is located in Lufkin, Texas and is 100% onsite. Company-sponsored relocation available.

Requirements

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

Nice To Haves

Candidates with experience in cardiology, cardiovascular medicine, internal medicine, or other specialty outpatient settings are strongly preferred.
Experience with EKGs/ECGs and phlebotomy is highly desirable.

Responsibilities

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 on an as-needed basis