{"schemaVersion":"jobsearcher.job.v1","id":"f3d4d3fdf0c915e7b41fa556","url":"https://jobsearcher.com/jobs/f3d4d3fdf0c915e7b41fa556","canonicalUrl":"https://jobsearcher.com/jobs/f3d4d3fdf0c915e7b41fa556","title":"Study Startup & Essential Documents Specialist","description":"Job Description\n\nA Trusted CRO Partner for the Future of Eye Careiuvo Clinical is a full-service ophthalmology-focused contract research organization (CRO) dedicated to improving patient's quality of life with breakthrough eye care therapies. We combine decades of specialized experience with a high touch, high science approach, partnering with innovators to accelerate ophthalmic breakthroughs from concept to commercialization. Whether advancing a novel retinal therapy or supporting a complex ocular device trial, we provide the expertise, flexibility, and personal dedication to ensure your clinical trial's success.We offer a comprehensive benefits package and the opportunity to broaden your experience and grow your career!We currently have an exciting opportunity for a Study Startup & Essential Documents Specialist .SUMMARYThe Study Startup and Essential Documents Specialist (SSEDS) is responsible for supporting site start-up activities, including collection and review of essential documents for assigned investigative sites and Central IRB activities on a project and site-level. As a member of the Clinical organization, the SSEDS is responsible for assigned clinical programs and sites.ESSENTIAL DUTIES AND RESPONSIBILITIESManage essential documents at a study-level from study start-up through close-out and at a site-level from site selection through close-out inclusive of IRB activitiesComplete activities to confirm study and site-level eTMF completeness and document quality Set-up and maintenance of study-specific Regulatory Trackers as needed (in lieu of an electronic tracking system)Ongoing review of Regulatory Trackers (or electronic tracking system)Responsible for Central IRB Management on a project and site-levelComplete Study-level IRB submissions inclusive of but not limited to: Assist with the development of Informed Consent Form and patient facing materials such as phone scripts, patient diaries, and advertisements as needed in preparation of study level IRB submission.Study-level close-out activities as applicableIndependently accountable for study start-up for assigned clinical sites Serve as the primary point of contact for assigned sites for start-upAssist sites with the completion of IRB applications and submissionsProvide guidance and instruction on site completion of essential documentsSend study start-up/required site activation documents to assigned clinical sitesOrganize, prepare, and ship applicable clinical study binders to clinical sites (regulatory binders, questionnaires, etc.) as neededCollect and carefully review essential documents in accordance with Sponsor specificationsResponsible for Essential Document Quality, Completeness, and Processing Verify documents meet ALCOAC standards and are aligned with ICH/GCP and SOP requirementsFollow study specific TMF Plan for classification of documents within the eTMFCollaborate with eTMF Administrator re: study-specific updates needed to the Veeva system as applicableFollow up with sites re: essential document action items through to resolutionTrack site essential documents and maintain study trackers as assigned to provide real-time updates to Sponsor as requestedPrimary point of contact for sites during the start-up process and essential document contact for the duration of the study (site activation forward)Responsible for site-level essential document Action Item (AI) follow-up with sites (e.g., start-up/site activation documents, expired documents, missing documents, document updates) from the time of site-selection through site close-outCollaborate with internal and external team members. Inclusive of but not limited to: Assist with eTMF follow-up required as a result of internal or external eTMF audits or site-level audit findings pertaining to the ISFAttend internal and external team calls to stay informed of current study status and provide feedback/updates as neededDevelop collaborative relationships with investigative sites and internal and external team members. Review pertinent regulations to develop and communicate proactive solutions to start-up issues and challenges.Provide recommendations for improvement of project or divisional efficiencies based on work experience and observationsEscalate site issues to applicable project team memberOther duties as assignedRead and adhere to client-approved or iuvo SOPsQUALIFICATIONS & REQUIREMENTSTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.EDUCATION and/or EXPERIENCEBachelor's degree or equivalent job experience preferredA clinical background with strong clinical site management/study start-up experienceExperience collecting, reviewing, and submitting regulatory documents and communicating with investigative sites is highly preferredExperience in ophthalmology preferred.COMPUTER SKILLSExperience working with eTMF systemsProficiency with Microsoft Office (Word, Excel, Outlook, Teams) and other software/programs as applicable to positionCOMMUNICATION SKILLSThis position requires a person who communicates effectively both verbally and in writing with clinicians, clients, vendors, and internal project team members through demonstration of:Excellent presentation and interpersonal skills, including clear, succinct, and timely communicationSharing ideas in a constructive mannerListening to and objectively considering ideas and suggestions from othersKeeping commitmentsKeeping others informed of work progress, timetables and issuesRead and comprehend work instructions/SOPs and protocols and write clear, concise communications and documentationOTHER SKILLS and ABILITIESHighly organizedMust be able to efficiently schedule/perform follow-up of tasks, manage multiple prioritiesExcellent time managementAttention to detailStrong analytical skillsPHYSICAL DEMANDSThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.While performing the duties of this job, the employee is regularly required to sit or stand at a desk, talk and hear.WORK ENVIRONMENTThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Office setting / remote home office. iuvo Clinical fosters a video-first environment; employees are expected to have their cameras on for all internal and external meetings, check-ins, and collaborative sessions.Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.LOCATION RemoteTRAVEL As required, estimated as DISCLAIMERThis job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.iuvo Clinical is an Equal Opportunity Employer","company":"Iuvo Bioscience Operations","rawCompany":"iuvo bioscience operations","city":"Chester","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-07-16T23:40:59.982Z","occupations":[{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"15-1299.03","title":"Document Management Specialists","slug":"document-management-specialists"},{"code":"13-1199.00","title":"Business Operations Specialists, All Other","slug":"business-operations-specialists-all-other"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"621111","title":"Offices of Physicians (except Mental Health Specialists)","slug":"offices-of-physicians-except-mental-health-specialists"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Study Startup & Essential Documents Specialist","description":"Job Description\n\nA Trusted CRO Partner for the Future of Eye Careiuvo Clinical is a full-service ophthalmology-focused contract research organization (CRO) dedicated to improving patient's quality of life with breakthrough eye care therapies. We combine decades of specialized experience with a high touch, high science approach, partnering with innovators to accelerate ophthalmic breakthroughs from concept to commercialization. Whether advancing a novel retinal therapy or supporting a complex ocular device trial, we provide the expertise, flexibility, and personal dedication to ensure your clinical trial's success.We offer a comprehensive benefits package and the opportunity to broaden your experience and grow your career!We currently have an exciting opportunity for a Study Startup & Essential Documents Specialist .SUMMARYThe Study Startup and Essential Documents Specialist (SSEDS) is responsible for supporting site start-up activities, including collection and review of essential documents for assigned investigative sites and Central IRB activities on a project and site-level. As a member of the Clinical organization, the SSEDS is responsible for assigned clinical programs and sites.ESSENTIAL DUTIES AND RESPONSIBILITIESManage essential documents at a study-level from study start-up through close-out and at a site-level from site selection through close-out inclusive of IRB activitiesComplete activities to confirm study and site-level eTMF completeness and document quality Set-up and maintenance of study-specific Regulatory Trackers as needed (in lieu of an electronic tracking system)Ongoing review of Regulatory Trackers (or electronic tracking system)Responsible for Central IRB Management on a project and site-levelComplete Study-level IRB submissions inclusive of but not limited to: Assist with the development of Informed Consent Form and patient facing materials such as phone scripts, patient diaries, and advertisements as needed in preparation of study level IRB submission.Study-level close-out activities as applicableIndependently accountable for study start-up for assigned clinical sites Serve as the primary point of contact for assigned sites for start-upAssist sites with the completion of IRB applications and submissionsProvide guidance and instruction on site completion of essential documentsSend study start-up/required site activation documents to assigned clinical sitesOrganize, prepare, and ship applicable clinical study binders to clinical sites (regulatory binders, questionnaires, etc.) as neededCollect and carefully review essential documents in accordance with Sponsor specificationsResponsible for Essential Document Quality, Completeness, and Processing Verify documents meet ALCOAC standards and are aligned with ICH/GCP and SOP requirementsFollow study specific TMF Plan for classification of documents within the eTMFCollaborate with eTMF Administrator re: study-specific updates needed to the Veeva system as applicableFollow up with sites re: essential document action items through to resolutionTrack site essential documents and maintain study trackers as assigned to provide real-time updates to Sponsor as requestedPrimary point of contact for sites during the start-up process and essential document contact for the duration of the study (site activation forward)Responsible for site-level essential document Action Item (AI) follow-up with sites (e.g., start-up/site activation documents, expired documents, missing documents, document updates) from the time of site-selection through site close-outCollaborate with internal and external team members. Inclusive of but not limited to: Assist with eTMF follow-up required as a result of internal or external eTMF audits or site-level audit findings pertaining to the ISFAttend internal and external team calls to stay informed of current study status and provide feedback/updates as neededDevelop collaborative relationships with investigative sites and internal and external team members. Review pertinent regulations to develop and communicate proactive solutions to start-up issues and challenges.Provide recommendations for improvement of project or divisional efficiencies based on work experience and observationsEscalate site issues to applicable project team memberOther duties as assignedRead and adhere to client-approved or iuvo SOPsQUALIFICATIONS & REQUIREMENTSTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.EDUCATION and/or EXPERIENCEBachelor's degree or equivalent job experience preferredA clinical background with strong clinical site management/study start-up experienceExperience collecting, reviewing, and submitting regulatory documents and communicating with investigative sites is highly preferredExperience in ophthalmology preferred.COMPUTER SKILLSExperience working with eTMF systemsProficiency with Microsoft Office (Word, Excel, Outlook, Teams) and other software/programs as applicable to positionCOMMUNICATION SKILLSThis position requires a person who communicates effectively both verbally and in writing with clinicians, clients, vendors, and internal project team members through demonstration of:Excellent presentation and interpersonal skills, including clear, succinct, and timely communicationSharing ideas in a constructive mannerListening to and objectively considering ideas and suggestions from othersKeeping commitmentsKeeping others informed of work progress, timetables and issuesRead and comprehend work instructions/SOPs and protocols and write clear, concise communications and documentationOTHER SKILLS and ABILITIESHighly organizedMust be able to efficiently schedule/perform follow-up of tasks, manage multiple prioritiesExcellent time managementAttention to detailStrong analytical skillsPHYSICAL DEMANDSThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.While performing the duties of this job, the employee is regularly required to sit or stand at a desk, talk and hear.WORK ENVIRONMENTThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Office setting / remote home office. iuvo Clinical fosters a video-first environment; employees are expected to have their cameras on for all internal and external meetings, check-ins, and collaborative sessions.Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.LOCATION RemoteTRAVEL As required, estimated as DISCLAIMERThis job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.iuvo Clinical is an Equal Opportunity Employer","datePosted":"2026-07-16T23:40:59.982Z","dateModified":"2026-07-16T23:40:59.982Z","hiringOrganization":{"@type":"Organization","name":"Iuvo Bioscience Operations","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Chester","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"f3d4d3fdf0c915e7b41fa556"},"url":"https://jobsearcher.com/jobs/f3d4d3fdf0c915e7b41fa556"}}