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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.

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><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>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 Springfield, Missouri<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>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

Clinical Research Coordinator II

GreenHouseAPI

With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.

HOUR

<p>Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37's extraordinary work environment allows continuous collaboration between clinicians, clinical researchers, patient recruitment specialists, data managers and technology developers. The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development and feasibility analysis to clinical trial implementation and closeout.</p><p>The <strong>Per Diem Mobile Research Nurse</strong> is a Registered Nurse who will work per diem and has experience across multiple therapeutic areas with the ability to work independently and integrate well with the Nursing Solutions Group. With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. The Mobile Research Nurse ensures the professional delivery of patient care in compliance with all federal and state regulations, Good Clinical Practice, and Standard Operating Procedures. </p><p>*This is a travel role that requires on-site visits to participants homes.</p><p>Duties for this position include but are not limited to:</p><ol><li>Participate and provide research nurse services to qualified study participants at home</li><li>Apply clinical research and nursing practices to develop solutions to complex problems</li><li>Collaborate with Lead and Per Diem Mobile Research Nurses on solutioning, education, and resource support</li><li>Participate in activities that will further the operational development of Science 37 nursing service delivery</li><li>Develop relationships with study team members and serve as the subject matter expert (SME) on all nursing processes</li><li>Other duties as assigned as the needs of Science 37 evolve and change</li></ol><p>This position has the following qualifications:</p><ol><li>BSN degree preferred</li><li>Full Vaccination Required subject to applicable law: All Science 37 personnel who interact in person with trial participants must be fully<br/>vaccinated against COVID-19."Fully vaccinated" means having received both doses of the Pfizer or Moderna vaccines or the single-dose Johnson & Johnson vaccine.</li><li>Active RN licensure in home state as well as eligibility for Compact Licensure required</li><li>Minimum 2+ years clinical/research experience preferred</li><li>Basic Life Support (BLS) Certification</li><li>Maintain a positive reflection of the company by representation in participant's homes or in clinic settings</li><li>Travel and availability qualifications are as follows<strong>:</strong><ol><li>1-2 days minimum a week dedicated to support Science 37's study visits
<ol><li>Weekday/night availability required</li></ol></li><li>Must be willing to travel to a participants homes </li><li>Active Driver's License</li></ol></li></ol><p>Science 37 is looking for people with the following skills and competencies:</p><ol><li>BSN degree preferred</li><li>Active RN licensure in home state as well as eligibility for Compact Licensure required</li><li>Minimum 2+ years clinical/research experience preferred</li><li>Basic Life Support (BLS) Certification</li><li>Active Driver's License</li><li>Weekday/night availability required</li><li>Maintain a positive reflection of the company by representation in participant's homes or in clinic settings</li><li>Up to 100% travel, as needed, for study participant visits, project team meetings, and other professional meetings/conferences as needed</li><li>Ability to obtain nursing license in multiple states based on study needs</li><li>Physical ability to perform nursing tasks and lift equipment up to 15 kg in weight</li><li>Access to a reliable vehicle to perform study participant visits and transport equipment</li><li>Ability to drive to local and/or remote locations to perform study participant visits</li><li>Ability to use technology effectively and appropriately for study participant assessments and documentation including but not limited to study participant care equipment, laptop computers, communication devices and tablets</li><li>Ability to communicate in English (both verbal and written)</li></ol><p>There is minimal supervision for this position, with individuals reporting to the Manager, Nursing Solutions Group.</p><p>Compensation varies based on location and work being performed. The starting pay range for a candidate selected for this position is generally within the range of $50-55 per hour. Employees may be eligible for additional discretionary bonuses and commissions. The successful candidate's actual pay will also be based on qualifications and experience, so the actual starting pay may be above or below this range.</p><p>Science 37 is an equal opportunity employer.  </p><p>We are committed to creating a diverse environment and is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to age, race, ethnicity (including but not limited to hair texture and protected hairstyles), ancestry, color, sex, national origin, sexual orientation, gender, gender identity, gender expression, transgender status, religious creed, physical or mental disability (including actual or perceived disability), medical condition (including HIV/AIDS), pregnancy, perceived pregnancy and pregnancy related conditions, genetic information, marital status, political affiliation or activities, status as a victim of domestic violence, assault, or stalking, veteran status or participation in the uniformed military services of the United States, including the National Guard, or any other basis prohibited by applicable law.</p><hr/><p style="text-align:justify">Science 37 values the well-being of its employees and aims to provide team members with everything they need to succeed. </p><p style="text-align:justify">Submit your resume to apply!</p><p style="text-align:justify"> </p><div class="content-conclusion"><p>To learn about Science 37's privacy practices including compliance with applicable privacy laws, please click <a href="https://science37.com/Privacy-Policy" rel="nofollow noopener noreferrer" target="_blank">here</a></p></div>

Science 37

Per Diem Clinical Research Nurse - Home Visits

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.

<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 Springfield, MO.</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>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>

Sub-Investigator

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Clinical Research Coordinator II Care Access

Per Diem Clinical Research Nurse - Home Visits Science 37

Sub-Investigator Care Access

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