UNKNOWN

FEED

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Perform trial procedures as per delegation which can include the following but not limited to: Prescreen study candidates by telephone and review exclusionary conditions or medications prior to scheduling screening appointment.

YEAR

<div class="content-intro"><p><strong>About Care Access</strong></p><p>Care Access is working to make the future of health better for all. <strong>With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. </strong>We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, <strong>and contribute to the medical breakthroughs of tomorrow.</strong></p><p>With programs like <em>Future of Medicine</em>, which makes advanced health screenings and research opportunities accessible to communities worldwide, and <em>Difference Makers</em>, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.</p><p>To learn more about Care Access, visit <a href="http://www.careaccess.com/" rel="nofollow">www.CareAccess.com</a>.</p></div><h3><strong>How This Role Makes a Difference</strong></h3><div><p>The Sub-Investigator will be responsible for regional travel mixed with remote tele-medicine work to support our clinical research studies. Additionally, our Sub-Investigator will be skilled in administering investigational products (IV, SC, TD, IM, PO administration), performing physical examinations, monitoring for investigational product related reactions, among other duties beyond the standard clinical research Sub-Investigator role. Care Access is looking for highly motivated Nurse Practitioners or Physician's Assistants to support clinical trial related activities in states throughout the USA.</p></div><div><h3><strong>How You'll Make An Impact</strong></h3><div><ul><li>Work closely with the Principal Investigator to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable.</li><li>Attends and participates in meetings with the director, other managers, and staff as necessary.</li><li>Complies with regulatory requirements, policies, procedures, and standards of practice.</li><li>Read and understand the informed consent form, protocol, and investigator's brochure.</li><li>Be available to see subjects virtually or in-person as dictated by project design, answer their questions, and resolve medical issues during the study visit.</li><li>Sign and ensure that the study documentation for each study visit is completed.</li><li>Perform all study responsibilities in compliance with the IRB approved protocol.</li><li>Administration of Investigational Products (via subcutaneous, transdermal, intramuscular, intravenous, or oral routes).</li><li>Proficiency in starting, monitoring, and maintaining intravenous lines.</li><li>Proficiency in phlebotomy, proper blood collection practices, and laboratory processing practices (can be learned)</li><li>Contribute as an active member of clinicians involved in the management of infusion or other investigational product related reactions.</li><li>Maintain a clean, efficient clinical area to assure the highest standards of patient care.</li><li>Follow safety and PPE procedures as well as maintain proper documentation of infusion procedures.</li><li>Timely communications with internal teams, investigators, review boards, and study subjects</li><li>Perform trial procedures as per delegation which can include the following but not limited to:</li><li>Prescreen study candidates by telephone and review exclusionary conditions or medications prior to scheduling screening appointment.</li><li>Obtain informed consent per SOP.</li><li>Administer delegated study questionnaires, as appropriate.</li><li>Collect and evaluate medical records.</li><li>Complete visit procedures and ensure proper specimen collection, processing, and shipment in accordance with protocol.</li><li>Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.</li><li>Review screening documentation and approves subjects for admission to study.</li><li>Review admission documentation and approves subject for randomization.</li><li>Provide ongoing assessment of the study subject/patient to identify Adverse Events.</li><li>Ensure that serious and unexpected adverse events are reported promptly to the Pl.</li><li>Review and evaluates all study data and comments to the clinical significance of any out-of-range results.</li><li>Perform physical examinations as part of screening evaluation and active study conduct.</li><li>Provide medical management of adverse events as appropriate.</li><li>Dispense study medication per protocol and/or IVRS systems. Educate patient on proper administration and importance of compliance.</li><li>Monitor patient progress on study medication.</li><li>Other duties as assigned.</li></ul></div><h3><strong>The Expertise Required</strong></h3><div><ul><li>Ability to check, perform, and document vitals as well as EKG (ECG)</li><li>Phlebotomy and expert IV skills</li><li>Excellent working knowledge of medical and research terminology</li><li>Excellent working knowledge of federal regulations, good clinical practices (GCP)</li><li>Ability to communicate and work effectively with a diverse team of professionals.</li><li>Strong organizational skills: Able to prioritize, support, and follow through on assignments with good understanding of medical terminology.</li><li>Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors.</li><li>Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors.</li><li>Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals.</li><li>Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.</li><li>Ability to balance tasks with competing priorities.</li><li>Critical thinker and problem solver.</li><li>Curiosity and passion to learn, innovative, and able to take thoughtful risks while communicating concerns and mitigations.</li><li>Good management and organizational skills, understanding of medical procedures.</li><li>Exceptional interpersonal skills, willingness to the ability to work independently.</li><li>Ability to lift a minimum of 50 pounds.</li><li>Command of professional and Business English (written and spoken).</li><li>You must have the authorization to work in the US for any employer.</li><li>You must not need visa sponsorship, either now or in the future.</li><li>You must live in the USA and be willing and able to travel with 24–36-hour notice</li></ul></div><div><div class="text-body text-muted"><strong>Certifications/Licenses, Education, and Experience</strong></div></div><div><ul><li>At least Master's Level Science Degree. Nurse Practitioner or Physician Assistant with 5+ years of clinical experience.</li><li>Clinical Practice Experience Desired with Infusion Skillset.</li><li>Currently licensed in good standing in one or more states.</li><li>A minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research setting.</li><li>Preferred at least one (1) year of experience as a Clinical Research Coordinator or willingness to learn.</li></ul></div><h3><strong>How We Work Together</strong></h3><ul><li><strong>Location</strong>: This is an on-site position with regional commute requirements, located in Dalton, GA.</li><li><strong>Travel</strong>: Regularly planned travel within the region will be required as part of the role. </li><li><strong>Physical demands associated with this position Include</strong>: The ability to use keyboards and other computer equipment.</li></ul><p style="text-align:center">The expected salary range for this role is $120,000 - $150,000 USD per year for full time team members.</p><h3><strong>Benefits & Perks (US Full Time Employees)</strong></h3><ul><li>Paid Time Off (PTO) and Company Paid Holidays</li><li>100% Employer paid medical, dental, and vision insurance plan options</li><li>Health Savings Account and Flexible Spending Accounts</li><li>Bi-weekly HSA employer contribution</li><li>Company paid Short-Term Disability and Long-Term Disability</li><li>401(k) Retirement Plan, with Company Match </li></ul></div><div class="content-conclusion"><p><strong>Diversity & Inclusion</strong></p><p>We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. </p><p>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.</p><p>Care Access is unable to sponsor work visas at this time.</p><p>If you need an accommodation to apply for a role with Care Access, please reach out to: </p><p>TalentAcquisition@careaccess.com</p><p/><p>Mandatory Employer Disclosures:<br/><strong>Notice to Illinois applicants:</strong> Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.<br/><strong>Notice to Connecticut applicants:</strong> Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.<br/><strong>Notice to Arizona, Georgia, Indiana, and North Dakota applicants:</strong> Care Access complies with applicable laws prohibiting smoking in and around places of employment.<br/><strong>Notice to Massachusetts applicants:</strong> It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.<br/><strong>Notice to Rhode Island applicants: </strong>Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.<br/><strong>Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. </strong></p></div>

Care Access

Sub-Investigator

Adverse Events

Blood Bank

Calendar Management

Clinical Assessment

Clinical Data

Clinical Medicine

Clinical Practices/Protocols

Clinical Research

Clinical Support

Clinical Trial

Communication Skills

Community Health

Community Support

Computer Skills

Dental Insurance

Documentation

Electrocardiogram

Electronic Data Capture (EDC)

English Language

Establish Priorities

Event Management

Federal Laws and Regulations

Follow Through

GCP (Good Clinical Practices)

Healthcare

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Informed Consent

Interpersonal Skills

Investigational New Drug (IND)

Keyboards

Laboratory Techniques

Maintain Compliance

Medical Records

Medical Research

Medical Terminology

Medical Treatment

Medications

Medicine

Microsoft Excel

Microsoft Word

Nurse Practitioner

Nursing

OSHA

Organizational Skills

Patient Administration

Patient Assessment

Patient Care

Patient Education

Phlebotomy

Physical Demands

Physician Assistant

Presentation/Verbal Skills

Problem Solving Skills

Project Design

Quality Assurance

Quality Control

Regulatory Requirements

Research Protocols

Safety Process

Sample/Specimen Processing

Specimen Collection

Standard Operating Procedures (SOP)

Standards of Care

State Laws and Regulations

Team Building

Team Lead/Manager

Team Player

Telemedicine

Time Management

Travel Planning

Vision Plan

Voice Response Systems

Willing to Travel

Writing Skills

GreenHouseAPI

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Certifications/Licenses, Education, and Experience:Previous experience as a Principal Investigator is required; 2 years prior experience as a Principal Investigator or Sub-Investigator, preferred .

<div class="content-intro"><p><strong>About Care Access</strong></p><p>Care Access is working to make the future of health better for all. <strong>With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. </strong>We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, <strong>and contribute to the medical breakthroughs of tomorrow.</strong></p><p>With programs like <em>Future of Medicine</em>, which makes advanced health screenings and research opportunities accessible to communities worldwide, and <em>Difference Makers</em>, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.</p><p>To learn more about Care Access, visit <a href="http://www.careaccess.com/" rel="nofollow">www.CareAccess.com</a>.</p></div><h3><strong>How This Role Makes a Difference</strong></h3><div><p>We are seeking a highly skilled and experienced Principal Investigator to join our team. As the Principal Investigator, you will be responsible for oversight of all clinical trials according to study protocols, company processes, and GCP.  </p></div><div><h3><strong>How You'll Make An Impact</strong></h3><ul><li>Provide overall medical oversight and medical review of protocols in conformance with good clinical practice 
<ul><li>Review sponsor provided safety reports.  </li><li>Review and maintain accurate case report forms.  </li></ul></li><li>Ensure that the safety and well-being of all participants in the study at the trial site are protected 
<ul><li>Assess subject response to therapy, evaluate and address adverse experiences   </li></ul></li><li>Perform physical assessments, examinations and study procedures as required by study protocols </li><li>Train Sub-Investigators and study staff members on protocol and protocol specific procedures. Provide medical support to sub-investigators and study staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.  <ul><li>Review the inclusion/exclusion criteria, endpoint criteria, and investigational product use with the internal research team. </li></ul></li><li>Complete the necessary Care Access and protocol specific trainings</li><li>Comply with ICH GCP (International Conference on Harmonization – Good Clinical Practice) and all applicable regulatory requirements </li><li>Participate in monitoring visits and sponsor meetings; allow monitoring and auditing by sponsors and inspection by appropriate regulatory agencies </li></ul><h3><strong>The Expertise Required</strong></h3><div><ul><li>Excellent written and verbal communication skills </li><li>Ability to effectively prioritize tasks in a fast-paced environment </li><li>Attention to detail and ability to maintain confidentiality when handling sensitive information. </li><li>Critical thinking, dynamic problem-solving skills </li></ul></div><div><div class="text-body text-muted"><strong>Certifications/Licenses, Education, and Experience:</strong></div></div><div><ul><li>Previous experience as a Principal Investigator is required; 2 years prior experience as a Principal Investigator or Sub-Investigator, preferred </li><li>Training and certification in Good Clinical Practice (GCP)</li><li>MD or DO with an active, unrestricted medical license (medical license must be valid in the state in which the research is conducted) </li></ul></div><h3><strong>How We Work Together</strong></h3><ul><li><strong>Location</strong>: Dalton, GA. This role requires 100% of work to be performed on site.</li><li><strong>Travel:</strong> This is an onsite position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.  </li><li><strong>Physical demands associated with this position Include</strong>: The ability to use keyboards and other computer equipment.
<ul><li>Walking - 20%</li><li>Standing - 20%</li><li>Sitting - 20%</li><li>Lifting - 20%
<ul><li>Up to 25 lbs, over 25 lbs, & overhead</li></ul></li><li>Driving - 20%</li><li>Exposure to blood borne pathogens - Yes</li></ul></li></ul><p style="text-align:center">The expected salary range for this role is $200,000 - $400,000 USD per year for full time team members.</p><h3><strong>Benefits & Perks (US Full Time Employees)</strong></h3><ul><li>Paid Time Off (PTO) and Company Paid Holidays</li><li>100% Employer paid medical, dental, and vision insurance plan options</li><li>Health Savings Account and Flexible Spending Accounts</li><li>Bi-weekly HSA employer contribution</li><li>Company paid Short-Term Disability and Long-Term Disability</li><li>401(k) Retirement Plan, with Company Match </li></ul></div><div class="content-conclusion"><p><strong>Diversity & Inclusion</strong></p><p>We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. </p><p>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.</p><p>Care Access is unable to sponsor work visas at this time.</p><p>If you need an accommodation to apply for a role with Care Access, please reach out to: </p><p>TalentAcquisition@careaccess.com</p><p/><p>Mandatory Employer Disclosures:<br/><strong>Notice to Illinois applicants:</strong> Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.<br/><strong>Notice to Connecticut applicants:</strong> Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.<br/><strong>Notice to Arizona, Georgia, Indiana, and North Dakota applicants:</strong> Care Access complies with applicable laws prohibiting smoking in and around places of employment.<br/><strong>Notice to Massachusetts applicants:</strong> It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.<br/><strong>Notice to Rhode Island applicants: </strong>Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.<br/><strong>Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. </strong></p></div>

Principal Investigator

Auditing

Blood-Borne Pathogens

Case Report Form (CRF)

Detail Oriented

Medical Office Administration

Medical Protocols

Patient Safety

Regulations

Reporting Skills

Research Skills

Safety/Work Safety

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

<div class="content-intro"><p><strong>About Care Access</strong></p><p>Care Access is working to make the future of health better for all. <strong>With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. </strong>We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, <strong>and contribute to the medical breakthroughs of tomorrow.</strong></p><p>With programs like <em>Future of Medicine</em>, which makes advanced health screenings and research opportunities accessible to communities worldwide, and <em>Difference Makers</em>, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.</p><p>To learn more about Care Access, visit <a href="http://www.careaccess.com/" rel="nofollow">www.CareAccess.com</a>.</p></div><div><h3><strong>How This Role Makes a Difference</strong></h3><p>The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. </p><div><h3><strong>How You'll Make An Impact</strong></h3><ul><li><strong>Patient Coordination</strong> <ul><li>Prioritize activities with specific regard to protocol timelines  </li><li>Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.  </li><li>Maintain effective relationships with study participants and other care Access Research personnel.  </li><li>Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.  </li><li>Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.  </li><li>Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)  </li><li>Prescreen study candidates   </li><li>Obtain informed consent per Care Access Research SOP .  </li><li>Complete visit procedures in accordance with protocol.  </li><li>Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.  </li><li>Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion. </li><li>Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.  <br/><br/></li></ul></li><li><strong>Documentation</strong> <ul><li>Record data legibly and enter in real time on paper or e-source documents  </li><li>Accurately record study medication inventory, medication dispensation, and patient compliance. </li><li>Resolve data management queries and correct source data within sponsor provided timelines </li><li>Assist regulatory personnel with completion and filing of regulatory documents. </li><li>Assist in the creation and review of source documents.  </li></ul></li></ul><ul><li><strong>Patient Recruitment</strong> 
<ul><li>Assist with planning and creation of appropriate recruitment materials.  </li><li>Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.  </li><li>Actively work with recruitment team in calling and recruiting subjects<br/><br/></li></ul></li><li>Review and assess protocol (including amendments) for clarity, logistical feasibility </li><li>Ensure that all training and study requirements are met prior to trial conduct</li><li>Communicate clearly verbally and in writing</li><li>Attend Investigator meetings as required</li><li>Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)  </li></ul><h3><strong>The Expertise Required</strong></h3><ul><li>Bilingual in Spanish required</li><li>Ability to understand and follow institutional SOPs.  </li><li>Excellent working knowledge of medical and research terminology  </li><li>Excellent working knowledge of federal regulations, good clinical practices (GCP)  </li><li>Ability to communicate and work effectively with a diverse team of professionals.  </li><li>Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail  </li><li>Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.  </li><li>Critical thinker and problem solver  </li><li>Friendly, outgoing personality; maintain a positive attitude under pressure.  </li><li>High level of self-motivation and energy  </li><li>Excellent professional writing and communication skills  </li><li>Ability to work independently in a fast-paced environment with minimal supervision.  </li></ul><div><div class="text-body text-muted"><strong>Certifications/Licenses, Education, and Experience:</strong></div></div><div><ul><li>Bachelor's Degree preferred, or equivalent combination of education, training and experience.  </li><li>A minimum of 3 years prior Clinical Research Coordinator experience required  </li><li>Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator    </li><li>Recent phlebotomy experience required  </li><li>Licenses: 
<ul><li>California based roles require National phlebotomy certification by an organization approved by the California Department of Public Health  </li><li>Louisiana based roles require National phlebotomy certification by an organization approved by the Louisiana State Board of Medical Examiners  </li><li>Washington based roles require National phlebotomy certification by an organization approved by the Washington State Department of Health  </li><li>Nevada based roles require Laboratory Assistant certification by the Division of Public and Behavioral Health  </li></ul></li></ul></div></div></div><h3><strong>How We Work Together</strong></h3><ul><li><strong>Location</strong>: This is an on-site position with regional commute requirements, located in Dalton, Georgia<ul><li><strong>Travel</strong>: This role requires up to 10% travel requirements further explained below. Length of travel will depend upon study requirements, staff needs, and company initiatives. 
<ul><li><strong>Type of travel required:</strong> ​Regional (within 100 miles)​ </li></ul></li><li><strong>Physical demands associated with this position Include</strong>: The ability to use keyboards and other computer equipment.<br/><ul><li>Walking - 20%</li><li>Standing - 20%</li><li>Sitting - 20%</li><li>Lifting - 20%
<ul><li>Up to 25lbs</li><li>Over 25lbs Overhead</li></ul></li><li>Driving - 20%</li></ul></li></ul></li></ul><div class="c-virtual_list__item" id="message-list_1763049962.052619"><div class="c-message_kit__background c-message_kit__background--hovered p-message_pane_message__message c-message_kit__message"><div class="c-message_kit__hover c-message_kit__hover--hovered"><div class="c-message_kit__actions c-message_kit__actions--default"><div class="c-message_actions__container c-message__actions"><div class="c-message_actions__group"><p style="text-align:center">The expected salary range for this role is $60,000 - $90,000 USD per year for full time team members.</p><h3><strong>Benefits & Perks (US Full Time Employees)</strong></h3><ul><li>Paid Time Off (PTO) and Company Paid Holidays</li><li>100% Employer paid medical, dental, and vision insurance plan options</li><li>Health Savings Account and Flexible Spending Accounts</li><li>Bi-weekly HSA employer contribution</li><li>Company paid Short-Term Disability and Long-Term Disability</li><li>401(k) Retirement Plan, with Company Match </li></ul></div></div></div></div></div></div><div class="content-conclusion"><p><strong>Diversity & Inclusion</strong></p><p>We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. </p><p>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.</p><p>Care Access is unable to sponsor work visas at this time.</p><p>If you need an accommodation to apply for a role with Care Access, please reach out to: </p><p>TalentAcquisition@careaccess.com</p><p/><p>Mandatory Employer Disclosures:<br/><strong>Notice to Illinois applicants:</strong> Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.<br/><strong>Notice to Connecticut applicants:</strong> Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.<br/><strong>Notice to Arizona, Georgia, Indiana, and North Dakota applicants:</strong> Care Access complies with applicable laws prohibiting smoking in and around places of employment.<br/><strong>Notice to Massachusetts applicants:</strong> It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.<br/><strong>Notice to Rhode Island applicants: </strong>Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.<br/><strong>Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. </strong></p></div>

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