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HomeCompaniesB16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001Research Assistant (RA)-FT

Research Assistant (RA)-FT

B16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001 · OCT-Ohio Clinical Trials, Columbus, OH, US, Columbus, OH · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyB16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001
TitleResearch Assistant (RA)-FT
Normalized title-
Department / team-
LocationOCT-Ohio Clinical Trials, OH, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-06-04 / 2026-06-03
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from B16edcc6 0faf 4d0b Be99 58eeae2d3d09 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in OCT-Ohio Clinical Trials.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 Us: 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. We are seeking a highly motivated PRN Research Assistant (RA) to join our team. You will be responsible for assisting with research studies, collecting and analyzing data, and ensuring compliance with study protocols. The Research Assistant will ensure compliance with protocol and overall clinical objectives. In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities: Assist with research studies by collecting and analyzing data Ensure compliance with study protocols and regulations Maintain accurate and complete records of research activities Prepare source documents for study visits. Perform vitals, ECGs, and phlebotomy. Data Entry from patient visit Manage lab kit inventory. Ship and process specimens Undertake protocol trainings as assigned. General office tasks such as filing, copying, and scanning. 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. Minimum Qualifications: High School Diploma or its equivalent; College degree preferred. 1 year of clinical experience is preferred. Strong organizational and communication skills Ability to work independently and as part of a team Attention to detail and accuracy Preferred Qualifications: Experience with clinical research studies Knowledge of regulatory requirements for research studies Knowledgeable in medical terminology

Full job record

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Org ID140b60bc-56c1-49a8-b09e-7f2ea335ec0c
Source ID6f0eabe0-f8d3-4a4c-b462-1d934416b9f7
Board ID6f0eabe0-f8d3-4a4c-b462-1d934416b9f7
Provideradp_workforcenow
Provider Job Key558132
TitleResearch Assistant (RA)-FT
Normalized Title
Statusactive
Activeyes
Location TextOCT-Ohio Clinical Trials, Columbus, OH, US, Columbus, OH
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionOH
CityOCT-Ohio Clinical Trials
Salary Raw
Salary Min
Salary Max
Salary Currency
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First Seen At2026-06-03 09:34:41Z
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 At2026-06-04 22:39:00Z
Source Updated At
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Parsed Structured
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Extensions
{}
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    "requisitionDescription": "<div><div><div><div><div><div><div><div><p style=\"margin:0in;font-family:Aptos;font-size:12.0pt;\"><strong><span style=\"font-family: arial, sans-serif; font-size: 14px;\">About Us:</span></strong></p><p style=\"margin:0in;font-family:Aptos;font-size:12.0pt;\"><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><br></span></p><p style=\"margin:0in;font-family:Aptos;font-size:12.0pt;\"><span style=\"font-family: arial, sans-serif; font-size: 14px;\">Evolution Research\nGroup (ERG) is dedicated to delivering high-quality Phase I&ndash;IV clinical trial\nexecution to help sponsors bring lifesaving and life-enhancing therapies to\nmarket quickly and safely. Founded in 2014, ERG has grown into a leading\nneuroscience clinical development company, with affiliate sites across the U.S.\nand deep expertise in clinical pharmacology, psychiatry, neurology, acute pain,\nand metabolic disorders. &nbsp;ERG has completed over 5,000 trials and\ncontinues to expand into high-need therapeutic areas in the U.S. and globally.</span></p><p style=\"margin:0in;font-family:Aptos;font-size:12.0pt;\"><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>&nbsp;</strong></span></p><p style=\"margin:0in;font-family:Aptos;font-size:12.0pt;\"><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>Why join us?&nbsp;</strong>We offer\na supportive culture, meaningful work, and the opportunity to contribute to\ncutting-edge research alongside industry leaders. Plus, we offer competitive\nbenefits include medical and dental coverage, a matching 401(k), and paid time off\nto recharge.&nbsp;</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><br></span></p><p style=\"margin:0in;font-family:Calibri;font-size:11.0pt;\"><span style=\"font-family: arial, sans-serif; font-size: 14px;\">We are seeking a highly motivated <strong>PRN Research Assistant (RA)</strong> to join our team. You will be responsible for assisting with research studies, collecting and analyzing data, and ensuring compliance with study protocols.&nbsp;</span><span style=\"box-sizing: border-box; color: rgba(0, 0, 0, 0.94); font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; font-family: arial, sans-serif;\">The Research Assistant will&nbsp;</span><span style=\"box-sizing: border-box; color: rgba(0, 0, 0, 0.94); font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; background-color: rgb(255, 255, 255); font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box; color: rgb(32, 33, 36);\">ensure compliance with protocol and overall clinical objectives.</span></span><span style=\"box-sizing: border-box; color: rgba(0, 0, 0, 0.94); font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; font-family: arial, sans-serif;\">&nbsp;In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.</span><span style=\"font-family: arial, sans-serif; font-size: 14px;\">&nbsp;</span></p><p><span style=\"font-family: arial,sans-serif;\"><strong><span style=\"font-size: 14px;\">Responsibilities:</span></strong></span></p><ul><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Assist with research studies by collecting and analyzing data</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Ensure compliance with study protocols and regulations</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Maintain accurate and complete records of research activities</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\">Prepare source documents for study&nbsp;</span></span></span><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\"><span style=\"box-sizing: border-box;\">visits.</span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\"><span style=\"box-sizing: border-box;\">Perform vitals, ECGs, and phlebotomy.</span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\">Data Entry from patient visit</span></span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\">Manage lab kit&nbsp;</span></span></span><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\"><span style=\"box-sizing: border-box;\">inventory.</span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\">Ship and process specimens</span></span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\">Undertake protocol trainings as assigned.</span></span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\">General office tasks such as filing, copying, and&nbsp;</span></span></span><span style=\"box-sizing: border-box; color: rgb(0, 0, 0);\"><span style=\"box-sizing: border-box;\">scanning.</span></span></li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\">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.</span></span></li></ul><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>Minimum Qualifications:</strong></span></p><ul><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\">High School Diploma or its equivalent; College degree preferred.</span></span></li><li style=\"font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\">1 year of clinical experience is preferred.</span></span></li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Strong organizational and communication skills</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Ability to work independently and as part of a team</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Attention to detail and accuracy</li></ul><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>Preferred Qualifications:</strong></span></p><ul><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Experience with clinical research studies</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Knowledge of regulatory requirements for research studies</li><li style=\"box-sizing: border-box; font-family: arial, sans-serif; font-size: 14px;\"><span style=\"box-sizing: border-box;\"><span style=\"box-sizing: border-box;\">Knowledgeable in medical terminology</span></span></li></ul><p><br></p></div></div></div></div></div></div></div></div>\n",
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