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.

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

Qualifications:

• 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

Additional Information

SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills, and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements, and individual qualifications and performance.

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: Clinical Research Coordinator (Lufkin, TX)

The Clinical Research Coordinator supports the clinical Principal Investigator (PI) and Clinical Research Nurse across multiple ongoing research studies. In this role, the study coordinator assists and facilitates daily clinical trial operations, playing a key part in successful study execution. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion. 

The position is located in Lufkin, Texas and is 100% onsite. Company-sponsored relocation available.

Responsibilities:

• Communicate with study participants regarding study objectives
• Conduct questionnaire administration and monitor participant compliance with study protocols
• Oversee study activities to ensure adherence to protocols, ethical conduct, and applicable regulatory standards
• Maintain research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
• Manage clinical study and staff records related to clinical study activity
• Manage participant screening and recruitment by scheduling study visits, obtaining informed consent, and conducting protocol-required intake assessments
• Track and manage participant enrollment across all site clinical studies
• Prepare trial-related document support such as protocol worksheets, adverse event reports, IRB documents, procedural manuals, and progress reports
• Maintain compliance of clinical studies with applicable local, state, and federal regulations, in alignment with ICH/GCP guidelines
• Create, organize, and maintain essential study documentation and records to ensure accuracy and compliance
• Communicate ongoing study progress to the Clinical PI and Site Operations leads, including updates on recruitment, compliance, and overall study performance
• Stay updated on the latest research protocols and regulatory requirements to ensure compliance and contribute to the successful completion of the study
• Willingness to travel on an as-needed basis.

Qualifications:

• Requires Bachelor’s degree in a relevant life science discipline
• 3+ years of previous experience working in clinical site/trials 
• Prior experience in the cardiology therapeutic area is a plus
• Knowledge of FDA & ICH GCP regulations and guidelines is required
• Detail-oriented and meticulous in all aspects of work 
• Strong follow-through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative
• Medical terminology and scientific knowledge are a plus
• Knowledge of standard clinical procedures and protocol
• Analytical mindset: needs analytical skills to collect and interpret data, taking note of patterns or outcomes that those in charge of the trial need to be aware of
• Excellent interpersonal skills, with the ability to effectively communicate and resolve issues while working with the PI, participants, and key stakeholders.
• Exceptional written and verbal communication skills, with the ability to clearly convey study requirements to participants and effectively liaise with site and management staff
• Skilled with standard computer programs including the MS Office suite.

Additional Information

SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills, and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements, and individual qualifications and performance.

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: Clinical Research Coordinator (Stockbridge, GA)

The Clinical Research Coordinator supports the clinical Principal Investigator (PI) and Clinical Research Nurse across multiple ongoing research studies. In this role, the study coordinator assists and facilitates daily clinical trial operations, playing a key part in successful study execution. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion. 

The position is located in Stockbridge, GA and is 100% onsite. Company-sponsored relocation available.

Responsibilities:

• Communicate with study participants regarding study objectives.

• Conduct questionnaire administration and monitor participant compliance with study protocols. 

• Oversee study activities to ensure adherence to protocols, ethical conduct, and applicable regulatory standards.

• Maintain research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines.

• Manage clinical study and staff records related to clinical study activity.

• Manage participant screening and recruitment by scheduling study visits, obtaining informed consent, and conducting protocol-required intake assessments.

• Track and manage participant enrollment across all site clinical studies.

• Prepare trial-related document support such as protocol worksheets, adverse event reports, IRB documents, procedural manuals, and progress reports.

• Maintain compliance of clinical studies with applicable local, state, and federal regulations, in alignment with ICH/GCP guidelines.

• Create, organize, and maintain essential study documentation and records to ensure accuracy and compliance.

• Communicate ongoing study progress to the Clinical PI and Site Operations leads, including updates on recruitment, compliance, and overall study performance.

• Stay updated on the latest research protocols and regulatory requirements to ensure compliance and contribute to the successful completion of the study.

• Willingness to travel on an as-needed basis.

Qualifications:

• Requires Bachelor’s degree in a relevant life science discipline

• 3+ years of previous experience working in clinical site/trials 

• Prior experience in the endocrinology therapeutic area is a plus. 

• Knowledge of FDA & ICH GCP regulations and guidelines is required

• Detail-oriented and meticulous in all aspects of work 

• Strong follow-through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative

• Medical terminology and scientific knowledge are a plus

• Knowledge of standard clinical procedures and protocol

• Analytical mindset: needs analytical skills to collect and interpret data, taking note of patterns or outcomes that those in charge of the trial need to be aware of

• Excellent interpersonal skills, with the ability to effectively communicate and resolve issues while working with the PI, participants, and key stakeholders.

• Exceptional written and verbal communication skills, with the ability to clearly convey study requirements to participants and effectively liaise with site and management staff

• Skilled with standard computer programs including the MS Office suite.

Additional Information

SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills, and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements, and individual qualifications and performance.

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: Clinical Research Coordinator (Lansing, MI)

The Clinical Research Coordinator supports the clinical Principal Investigator (PI) and Clinical Research Nurse across multiple ongoing research studies. In this role, the study coordinator assists and facilitates daily clinical trial operations, playing a key part in successful study execution. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion. 

This position is part-time. The position is located in Lansing, MI and is 100% onsite. Company-sponsored relocation available.

Responsibilities:

• Communicate with study participants regarding study objectives.
• Conduct questionnaire administration and monitor participant compliance with study protocols. 
• Oversee study activities to ensure adherence to protocols, ethical conduct, and applicable regulatory standards.
• Maintain research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines.
• Manage clinical study and staff records related to clinical study activity.
• Manage participant screening and recruitment by scheduling study visits, obtaining informed consent, and conducting protocol-required intake assessments.
• Track and manage participant enrollment across all site clinical studies.
• Prepare trial-related document support such as protocol worksheets, adverse event reports, IRB documents, procedural manuals, and progress reports.
• Maintain compliance of clinical studies with applicable local, state, and federal regulations, in alignment with ICH/GCP guidelines.
• Create, organize, and maintain essential study documentation and records to ensure accuracy and compliance.
• Communicate ongoing study progress to the Clinical PI and Site Operations leads, including updates on recruitment, compliance, and overall study performance.
• Stay updated on the latest research protocols and regulatory requirements to ensure compliance and contribute to the successful completion of the study.
• Willingness to travel on an as-needed basis.

Qualifications:

• Requires Bachelor’s degree in a relevant life science discipline
• 3+ years of previous experience working in clinical site/trials 
• Prior experience in the nephrology therapeutic area is a plus. 
• Knowledge of FDA & ICH GCP regulations and guidelines is required
• Detail-oriented and meticulous in all aspects of work 
• Strong follow-through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative
• Medical terminology and scientific knowledge are a plus
• Knowledge of standard clinical procedures and protocol
• Analytical mindset: needs analytical skills to collect and interpret data, taking note of patterns or outcomes that those in charge of the trial need to be aware of
• Excellent interpersonal skills, with the ability to effectively communicate and resolve issues while working with the PI, participants, and key stakeholders.
• Exceptional written and verbal communication skills, with the ability to clearly convey study requirements to participants and effectively liaise with site and management staff
• Skilled with standard computer programs including the MS Office suite.

Additional Information

SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills, and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements, and individual qualifications and performance.