Clinical Research Coordinator

{
  "content_hash": "712ec8b28f066cfdf35a133fb243f4d374697c1b07539215db554676f7c9e4ce",
  "source_hash": "eeba1828beace4471307166e7808380ff2723ed1e96a108c3001d6d59f26eb0b",
  "last_changed_at": "2026-05-31T19:05:58.612Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Pinehurst - Pinehurst, NC 28374; 205 Page Road, Pinehurst, NC, 28374, USA",
    "city": "Pinehurst",
    "region": "NC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": 50000,
  "salary_min": 42241.2,
  "inferred_at": "2026-06-06T20:00:44.565Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Pinehurst - Pinehurst, NC 28374; 205 Page Road, Pinehurst, NC, 28374, USA",
      "city": "Pinehurst",
      "region": "NC",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "year",
  "workplace_type": null,
  "salary_currency": "USD"
}

{}

{
  "detail": {
    "city": "Pinehurst",
    "jobId": 310059,
    "level": "",
    "endDate": "",
    "legalId": 4180,
    "isHotJob": false,
    "jobShift": "Day",
    "jobTitle": "Clinical Research Coordinator",
    "location": "Pinehurst - Pinehurst, NC 28374",
    "startDate": "",
    "clientCode": "0YR28",
    "remoteType": "",
    "description": "<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><strong>JOB SUMMARY</strong> </span></span></p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs, and GCPs.&nbsp; &nbsp; </span></span></p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><strong>RESPONSIBILITIES</strong></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Provide clinical research support to investigators to prepare for and execute assigned research studies, including:</span></span></span>\r\n\r\n\t<ul style=\"list-style-type:circle;\">\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Recruit and screen participants for clinical trials and maintain subject screening logs.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Maintain source documentation based on protocol requirements.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Schedule and execute study visits and perform study procedures.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Correspond with research subjects and troubleshoot study-related questions or issues.</span></span></span></li>\r\n\t\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Participate in &ldquo;huddles&rdquo; to confirm daily study tasks are assigned to team members and are executed to the expected standards.</span></span></span></li>\r\n\t</ul>\r\n\t</li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Assist with study data quality checking and query resolution.</span></span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation</span><span style=\"color:#2b3a42;\">, and cardiac telemetry </span><span style=\"color:#000000;\">monitoring, if needed. &nbsp;</span></span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Assist the investigator in verifying that research study objectives are met on time, within budget, and according to applicable protocol requirements, clinical research regulations, and quality standards.</span></span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Provide training to new investigator site staff members on study-specific topics and requirements. &nbsp;Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.</span></span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.</span></span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Assist the research site with coverage planning related to staffing and scheduling for research studies.</span></span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Monitor subject safety and report adverse reactions to appropriate medical personnel.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Maintain confidentiality of data and PHI as required.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Collaborate with provider offices to carry out research in the most efficient workflow possible.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Maintains stock of supplies needed to carry out each study per protocol.</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"color:#000000;\">Performs other duties and projects as assigned.</span></span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n",
    "jobCategory": "",
    "salaryRange": "$42,241.20 - $50,000.00 Salary/year",
    "socialMedia": {
      "xLink": null,
      "emailLink": null,
      "facebookLink": null,
      "linkedInLink": null
    },
    "isQuickApply": false,
    "positionType": "Full Time",
    "countryPaidIn": "",
    "googleJobJson": "{\"@context\":\"https://schema.org/\",\"@type\":\"JobPosting\",\"title\":\"Clinical Research Coordinator\",\"identifier\":\"J0YR28310059\",\"url\":\"https://www.paycomonline.net/v4/ats/web.php/portal/7FFF47DDEE1CED63F9886A868F7343EA/jobs/310059\",\"image\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=7FFF47DDEE1CED63F9886A868F7343EA\",\"baseSalary\":{\"@type\":\"MonetaryAmount\",\"currency\":\"USD\",\"value\":{\"@type\":\"QuantitativeValue\",\"minValue\":42241.2,\"maxValue\":50000,\"unitText\":\"\"}},\"datePosted\":\"2026-05-26\",\"description\":\"Job DetailsJob Location: Pinehurst - Pinehurst, NC 28374Position Type: Full TimeEducation Level: Bachelor's DegreeSalary Range: $42,241.20 - $50,000.00 Salary/yearJob Shift: DayJOB SUMMARY \\r\\n\\r\\nA Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs, and GCPs.&nbsp; &nbsp; \\r\\n\\r\\n&nbsp;\\r\\n\\r\\nRESPONSIBILITIES\\r\\n\\r\\n\\r\\n\\tProvide clinical research support to investigators to prepare for and execute assigned research studies, including:\\r\\n\\r\\n\\t\\r\\n\\t\\tCollect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.\\r\\n\\t\\tCollect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.\\r\\n\\t\\tRecruit and screen participants for clinical trials and maintain subject screening logs.\\r\\n\\t\\tAssist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.\\r\\n\\t\\tMaintain source documentation based on protocol requirements.\\r\\n\\t\\tSchedule and execute study visits and perform study procedures.\\r\\n\\t\\tHandle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.\\r\\n\\t\\tMonitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.\\r\\n\\t\\tCorrespond with research subjects and troubleshoot study-related questions or issues.\\r\\n\\t\\tParticipate in &ldquo;huddles&rdquo; to confirm daily study tasks are assigned to team members and are executed to the expected standards.\\r\\n\\t\\r\\n\\t\\r\\n\\tAssist with study data quality checking and query resolution.\\r\\n\\tPerform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed. &nbsp;\\r\\n\\tAssist the investigator in verifying that research study objectives are met on time, within budget, and according to applicable protocol requirements, clinical research regulations, and quality standards.\\r\\n\\tProvide training to new investigator site staff members on study-specific topics and requirements. &nbsp;Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.\\r\\n\\tPrepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.\\r\\n\\tAssist the research site with coverage planning related to staffing and scheduling for research studies.\\r\\n\\tMonitor subject safety and report adverse reactions to appropriate medical personnel.\\r\\n\\tMaintain confidentiality of data and PHI as required.\\r\\n\\tCollaborate with provider offices to carry out research in the most efficient workflow possible.\\r\\n\\tMaintains stock of supplies needed to carry out each study per protocol.\\r\\n\\tPerforms other duties and projects as assigned.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\nQualificationsQUALIFICATIONS\\r\\n\\r\\n\\r\\n\\tBachelor&#39;s degree in a related field\\r\\n\\t1-2 years of clinical research experience\\r\\n\\tRelevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience&nbsp;&nbsp;&nbsp;&nbsp;\\r\\n\\tProficient in the use of Microsoft Office applications\\r\\n\\tUnderstanding of medical terminology\\r\\n\\tWorking knowledge of clinical trials&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;\\r\\n\\tKnowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.\\r\\n\\tIn-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; \\r\\n\\tSkilled in carrying out required clinical procedures such as phlebotomy and vital signs.\\r\\n\\tStrong written and verbal communication skills including good command of the English language.\\r\\n\\tSkill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care.&nbsp; \\r\\n\\tSkill in preparing/maintaining records, writing reports, and responding to correspondence. \\r\\n\\tAbility to maintain quality control standards. \\r\\n\\tAbility to react calmly and effectively in all situations. \\r\\n\\tExcellent organizational and problem-solving skills.\\r\\n\\tEffective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.\\r\\n\\tAbility to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.&nbsp;&nbsp; \\r\\n\\tPractice a high level of integrity, honesty, and in maintaining confidentiality.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\n\\r\\nBENEFITS (Full-Time)\\r\\n\\r\\n\\r\\n\\tCompetitive salary\\r\\n\\tHealth Insurance\\r\\n\\tDental Insurance\\r\\n\\tDisability Insurance\\r\\n\\tLife Insurance\\r\\n\\tPaid Time Off\\r\\n\\tVision Insurance\\r\\n\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWORKING CONDITIONS\\r\\n\\r\\nThis job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting.&nbsp; Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination.&nbsp; Requires standing and walking for extensive periods of time.&nbsp; Occasionally lifts and carries items weighing up to 50 pounds.&nbsp; Requires corrected vision and hearing to normal range.&nbsp; \\r\\n\\r\\n&nbsp;\\r\\n\\r\\nDue to the nature of this position, employees are expected to work in person.&nbsp; This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary.&nbsp; Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nThe above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP&#39;s, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nApplicants must be authorized to work for ANY employer in the U.S. Innovo Research is unable to sponsor or take over sponsorship of an employment Visa at this time.\\r\\n\",\"responsibilities\":\"JOB SUMMARY \\r\\n\\r\\nA Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs, and GCPs.&nbsp; &nbsp; \\r\\n\\r\\n&nbsp;\\r\\n\\r\\nRESPONSIBILITIES\\r\\n\\r\\n\\r\\n\\tProvide clinical research support to investigators to prepare for and execute assigned research studies, including:\\r\\n\\r\\n\\t\\r\\n\\t\\tCollect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.\\r\\n\\t\\tCollect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.\\r\\n\\t\\tRecruit and screen participants for clinical trials and maintain subject screening logs.\\r\\n\\t\\tAssist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.\\r\\n\\t\\tMaintain source documentation based on protocol requirements.\\r\\n\\t\\tSchedule and execute study visits and perform study procedures.\\r\\n\\t\\tHandle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.\\r\\n\\t\\tMonitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.\\r\\n\\t\\tCorrespond with research subjects and troubleshoot study-related questions or issues.\\r\\n\\t\\tParticipate in &ldquo;huddles&rdquo; to confirm daily study tasks are assigned to team members and are executed to the expected standards.\\r\\n\\t\\r\\n\\t\\r\\n\\tAssist with study data quality checking and query resolution.\\r\\n\\tPerform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed. &nbsp;\\r\\n\\tAssist the investigator in verifying that research study objectives are met on time, within budget, and according to applicable protocol requirements, clinical research regulations, and quality standards.\\r\\n\\tProvide training to new investigator site staff members on study-specific topics and requirements. &nbsp;Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.\\r\\n\\tPrepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.\\r\\n\\tAssist the research site with coverage planning related to staffing and scheduling for research studies.\\r\\n\\tMonitor subject safety and report adverse reactions to appropriate medical personnel.\\r\\n\\tMaintain confidentiality of data and PHI as required.\\r\\n\\tCollaborate with provider offices to carry out research in the most efficient workflow possible.\\r\\n\\tMaintains stock of supplies needed to carry out each study per protocol.\\r\\n\\tPerforms other duties and projects as assigned.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\",\"employmentType\":\"FULL_TIME\",\"hiringOrganization\":{\"@type\":\"Organization\",\"name\":\"INNOVO RESEARCH INC\",\"logo\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=7FFF47DDEE1CED63F9886A868F7343EA\"},\"jobLocation\":{\"@type\":\"Place\",\"address\":{\"streetAddress\":\"205 Page Road\",\"addressLocality\":\"Pinehurst\",\"addressRegion\":\"NC\",\"postalCode\":28374,\"addressCountry\":\"USA\"}},\"qualifications\":\"QUALIFICATIONS\\r\\n\\r\\n\\r\\n\\tBachelor&#39;s degree in a related field\\r\\n\\t1-2 years of clinical research experience\\r\\n\\tRelevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience&nbsp;&nbsp;&nbsp;&nbsp;\\r\\n\\tProficient in the use of Microsoft Office applications\\r\\n\\tUnderstanding of medical terminology\\r\\n\\tWorking knowledge of clinical trials&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;\\r\\n\\tKnowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.\\r\\n\\tIn-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; \\r\\n\\tSkilled in carrying out required clinical procedures such as phlebotomy and vital signs.\\r\\n\\tStrong written and verbal communication skills including good command of the English language.\\r\\n\\tSkill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care.&nbsp; \\r\\n\\tSkill in preparing/maintaining records, writing reports, and responding to correspondence. \\r\\n\\tAbility to maintain quality control standards. \\r\\n\\tAbility to react calmly and effectively in all situations. \\r\\n\\tExcellent organizational and problem-solving skills.\\r\\n\\tEffective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.\\r\\n\\tAbility to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.&nbsp;&nbsp; \\r\\n\\tPractice a high level of integrity, honesty, and in maintaining confidentiality.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\n\\r\\nBENEFITS (Full-Time)\\r\\n\\r\\n\\r\\n\\tCompetitive salary\\r\\n\\tHealth Insurance\\r\\n\\tDental Insurance\\r\\n\\tDisability Insurance\\r\\n\\tLife Insurance\\r\\n\\tPaid Time Off\\r\\n\\tVision Insurance\\r\\n\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWORKING CONDITIONS\\r\\n\\r\\nThis job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting.&nbsp; Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination.&nbsp; Requires standing and walking for extensive periods of time.&nbsp; Occasionally lifts and carries items weighing up to 50 pounds.&nbsp; Requires corrected vision and hearing to normal range.&nbsp; \\r\\n\\r\\n&nbsp;\\r\\n\\r\\nDue to the nature of this position, employees are expected to work in person.&nbsp; This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary.&nbsp; Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nThe above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP&#39;s, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nApplicants must be authorized to work for ANY employer in the U.S. Innovo Research is unable to sponsor or take over sponsorship of an employment Visa at this time.\\r\\n\",\"experienceRequirements\":\"QUALIFICATIONS\\r\\n\\r\\n\\r\\n\\tBachelor&#39;s degree in a related field\\r\\n\\t1-2 years of clinical research experience\\r\\n\\tRelevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience&nbsp;&nbsp;&nbsp;&nbsp;\\r\\n\\tProficient in the use of Microsoft Office applications\\r\\n\\tUnderstanding of medical terminology\\r\\n\\tWorking knowledge of clinical trials&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;\\r\\n\\tKnowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.\\r\\n\\tIn-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; \\r\\n\\tSkilled in carrying out required clinical procedures such as phlebotomy and vital signs.\\r\\n\\tStrong written and verbal communication skills including good command of the English language.\\r\\n\\tSkill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care.&nbsp; \\r\\n\\tSkill in preparing/maintaining records, writing reports, and responding to correspondence. \\r\\n\\tAbility to maintain quality control standards. \\r\\n\\tAbility to react calmly and effectively in all situations. \\r\\n\\tExcellent organizational and problem-solving skills.\\r\\n\\tEffective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.\\r\\n\\tAbility to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.&nbsp;&nbsp; \\r\\n\\tPractice a high level of integrity, honesty, and in maintaining confidentiality.\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\n\\r\\nBENEFITS (Full-Time)\\r\\n\\r\\n\\r\\n\\tCompetitive salary\\r\\n\\tHealth Insurance\\r\\n\\tDental Insurance\\r\\n\\tDisability Insurance\\r\\n\\tLife Insurance\\r\\n\\tPaid Time Off\\r\\n\\tVision Insurance\\r\\n\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWORKING CONDITIONS\\r\\n\\r\\nThis job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting.&nbsp; Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination.&nbsp; Requires standing and walking for extensive periods of time.&nbsp; Occasionally lifts and carries items weighing up to 50 pounds.&nbsp; Requires corrected vision and hearing to normal range.&nbsp; \\r\\n\\r\\n&nbsp;\\r\\n\\r\\nDue to the nature of this position, employees are expected to work in person.&nbsp; This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary.&nbsp; Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nThe above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP&#39;s, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nApplicants must be authorized to work for ANY employer in the U.S. Innovo Research is unable to sponsor or take over sponsorship of an employment Visa at this time.\\r\\n\",\"validThrough\":\"-0001-11-30\",\"workHours\":\"Day\",\"educationRequirements\":\"Bachelor's Degree\"}",
    "applyAvailable": true,
    "educationLevel": "Bachelor's Degree",
    "qualifications": "<p><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\"><strong><span style=\"color:#000000;\">QUALIFICATIONS</span></strong></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\"><span style=\"color:#000000;\">Bachelor&#39;s degree in a related field</span></span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\"><span style=\"color:#000000;\">1-2 years of clinical research experience</span></span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience&nbsp;&nbsp;&nbsp;&nbsp;</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Proficient in the use of Microsoft Office applications</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Understanding of medical terminology</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Working knowledge of clinical trials&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span>&nbsp;</li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Knowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Skilled in carrying out required clinical procedures such as phlebotomy and vital signs.</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Strong written and verbal communication skills including good command of the English language.</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Skill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care.&nbsp; </span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Skill in preparing/maintaining records, writing reports, and responding to correspondence. </span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Ability to maintain quality control standards. </span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Ability to react calmly and effectively in all situations. </span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Excellent organizational and problem-solving skills.</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.</span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.&nbsp;&nbsp; </span></span></li>\r\n\t<li><span style=\"font-family:Arial, Helvetica, sans-serif;\"><span style=\"font-size:12px;\">Practice a high level of integrity, honesty, and in maintaining confidentiality.</span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<div>\r\n<p><strong>BENEFITS (Full-Time)</strong></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Competitive salary</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Health Insurance</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Dental Insurance</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Disability Insurance</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Life Insurance</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Aptos, sans-serif;\">Paid Time Off</span></span></li>\r\n\t<li><span style=\"font-size:12px;\"><span style=\"font-family:Aptos, sans-serif;\">Vision Insurance</span></span></li>\r\n</ul>\r\n</div>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><strong>WORKING CONDITIONS</strong></span></span></p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting.&nbsp; Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination.&nbsp; Requires standing and walking for extensive periods of time.&nbsp; Occasionally lifts and carries items weighing up to 50 pounds.&nbsp; Requires corrected vision and hearing to normal range.&nbsp; </span></span></p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Due to the nature of this position, employees are expected to work in person.&nbsp; This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary.&nbsp; Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.</span></span></p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP&#39;s, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.</span></span></p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12px;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Applicants must be authorized to work for ANY employer in the U.S. Innovo Research is unable to sponsor or take over sponsorship of an employment Visa at this time.</span></span></p>\r\n",
    "descriptionTitle": "Description",
    "travelPercentage": "",
    "jobYoutubeVideoId": "",
    "legalRevisionDate": {
      "date": "2022-06-22T06:33:03.000Z",
      "timezone": "America/Chicago",
      "timezone_type": 3
    },
    "secondaryLocations": [],
    "primaryPhoneCountry": "US",
    "primaryPhoneEnabled": true,
    "qualificationsTitle": "Qualifications",
    "primaryPhoneRequired": true,
    "primaryPhoneNumberDoesNotExist": false
  },
  "preview": {
    "jobId": 310059,
    "isHotJob": false,
    "jobTitle": "Clinical Research Coordinator",
    "postedOn": "",
    "locations": "Pinehurst - Pinehurst, NC 28374",
    "remoteType": "",
    "description": "JOB SUMMARY \r\n\r\nA Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, bot...",
    "positionType": "Full Time"
  },
  "detail_meta": {
    "url": "https://portal-applicant-tracking.us-cent.paycomonline.net/api/ats/job-postings/310059",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 45992
  },
  "detail_errors": []
}