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Clinical Research Coordinator-FT

B16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001 · Brain Matters Research DelRay, Delray Beach, FL, US, Delray Beach, FL · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyB16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001
TitleClinical Research Coordinator-FT
Normalized title-
Department / team-
LocationBrain Matters Research DelRay, FL, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-06-03 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Brain Matters Research DelRay.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyB16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001
Source6f0eabe0-f8d3-4a4c-b462-1d934416b9f7
ATS providerADP Workforce Now Recruiting

Description

About Company: Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally. Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge. Job Description: The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities: General Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study. Assist to develop draft source documents and review the documents for accuracy and clarity prior to study start up. Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study. Manage studies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements. Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment. Contribute to the SOP review and development as delegated by the Site Director. Study Management Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director. Attend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director. In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required. Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator Review and obtain informed consent from with potential study volunteer Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations Maintain organized, accurate and complete study records Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects. Enter data as appropriate for protocol (paper-electronic data capture) In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol. Perform study close-out procedures. Store study records appropriately Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives. Skills and Qualifications: Education and experience High School Diploma or its equivalent; College degree preferred. Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner. 1-2 years of clinical research experience preferred. Knowledgeable in medical terminology to communicate with physician office and laboratory staff. Demonstrate the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy. Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change. Requirements Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines. Excellent communication skills (interpersonal, written, verbal) Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

Full job record

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TitleClinical Research Coordinator-FT
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Activeyes
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First Seen At2026-05-31 18:35:35Z
Last Seen At2026-06-06 13:01:53Z
Last Checked At2026-06-06 13:01:53Z
Last Changed At2026-06-06 13:01:53Z
Inactive At—
Source Posted At2026-06-03 00:14:00Z
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    "requisitionDescription": "<div><div><div><div><div><p id=\"isPasted\"><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong style=\"box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: var(--tw-empty,/*!*/ /*!*/); --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000;\"><span style=\"box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: var(--tw-empty,/*!*/ /*!*/); --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000;\">About Company:</span></strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\">Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I&ndash;IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. &nbsp;ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>Why join us?</strong> We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.&nbsp;</span></p><p id=\"isPasted\"><span style=\"font-size: 14px;\"><span style=\"font-family: arial, sans-serif;\"><strong><span style=\"color:#000000;\">Job Description:</span></strong></span></span></p><p><span style=\"font-size: 14px;\"><span style=\"font-family: arial, sans-serif;\">The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.</span></span></p><p><span style=\"font-size: 14px;\"><span style=\"font-family: tahoma, sans-serif;\"><strong>Responsibilities:</strong></span></span></p><p style=\"text-align:justify;\"><span style=\"font-size: 14px;\"><span style=\"font-family: tahoma, sans-serif;\"><strong>General</strong></span></span></p><ul><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Obtain&nbsp;detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Assist to develop draft source documents and review the documents for accuracy and clarity prior to study start up.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Review&nbsp;with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Manage&nbsp;studies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.&nbsp;</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Contribute to the SOP review and development as delegated by the Site Director.&nbsp;</li></ul><p style=\"text-align:justify;\"><span style=\"font-size: 14px;\"><span style=\"font-family: tahoma, sans-serif;\"><strong>Study Management</strong>&nbsp;</span></span></p><ul><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Attend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director.&nbsp;</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Review and obtain informed consent from with potential study volunteer</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Maintain organized, accurate and complete study records</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Enter data as appropriate for protocol (paper-electronic data capture)</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Perform study close-out procedures.</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Store study records appropriately</li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\">Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG&rsquo;s objectives.</li></ul><p><span style=\"font-size: 14px;\"><span style=\"font-family: tahoma, sans-serif;\"><strong>Skills and Qualifications:</strong></span></span></p><ul><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\"><strong>Education and experience</strong><ul style=\"list-style-type: circle; font-family: initial; font-size: initial;\"><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">High School Diploma or its equivalent; College degree preferred.</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.&nbsp;</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">1-2 years of clinical research experience preferred.</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Knowledgeable in medical terminology to communicate with physician office and laboratory staff.&nbsp;</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Demonstrate&nbsp;the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.</li></ul></li><li style=\"text-align: justify; font-family: tahoma, sans-serif; font-size: 14px;\"><strong>Requirements</strong><ul style=\"list-style-type: circle; font-family: initial; font-size: initial;\"><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.&nbsp;</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Excellent communication skills (interpersonal, written, verbal)&nbsp;</li><li style=\"font-family: tahoma, sans-serif; font-size: 14px;\">Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)</li></ul></li></ul></div></div></div></div></div>\n",
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