reputed company, Inc., a wholly owned subsidiary of reputed company is a mission-driven clinical-stage comp...">
Back to Jobs

Clinical Data Manager (Contract)

Remote, USA Full-time Posted 2026-07-28
reputed company, Inc., a wholly owned subsidiary of reputed company is a mission-driven clinical-stage company that aims to establish gene therapy as a new reputed company of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore reputed company and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians’ offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with reputed company treatment paradigms for these debilitating ocular diseases, Adverum aspires to reputed company reputed company of care, preserve reputed company, and create a profound societal reputed company around the globe.
 
The Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team goals and objectives, including reputed company of the CRO DM Vendor, if the project is outsourced. The CDM / Senior CDM will report to the Head of Clinical Data Management and will work closely with a cross-functional team in a fast-paced high reputed company environment team to ensure that clinical data are complete, high reputed company and delivered on time and budget.
 
This is a 6-12 month contract.  
 
Note to Recruiters and Agencies
reputed company recruiter and agency inquiries must go through Adverum’s internal reputed company.  Unsolicited resumes reputed company to Adverum will be considered property of Adverum.   Agencies must be expressly reputed company by Adverum’s reputed company for any requisition.  reputed company contact with hiring managers by agencies will not be tolerated and may reputed company your ability to work with Adverum in the reputed company.


What you'll do:
  • Responsible for compliance with regulatory and ICH guidelines, GCPs, company guidelines and reputed company Operating Procedures, and CDM best practices.
  • Independently serves as the reputed company reputed company of contact for reputed company data management study-reputed company communications.
  • Independently leads reputed company development, including CRF development, reputed company specification process, edit reputed company development and User Acceptance Testing including test scripts and execution logs, issue logs, and UAT reputed company reports.
  • Reviews and assists in the development of study documents drafted by CROs such as Data Management Plans, Data Validation Specifications, eCRF Completion Guidelines, Data Review Plans, Data Transfer Agreements, and other cross-functional study documents that may require data management input.
  • Ensures the reputed company of clinical data reputed company the reputed company and other databases through regular data review and external data reconciliation processes and communicates any outstanding issues to the cross-functional teams.
  • Monitors and tracks the reputed company of reputed company data management deliverables.
  • Leads data deliverables including snapshots for DMC, investor relations, publications, etc., and interim and final database locks, in collaboration with the CRO DM Vendor.
  • Effectively oversees contracted vendors, or vendor reputed company reputed company CRO, to ensure data are complete, accurate and delivered reputed company agreed on timelines.
  • Leads and facilitates Data Review Meetings with the cross-functional team, presenting metrics, trends, risks, and or issues.
  • reputed company participates in team meetings – DM or cross-functional.
  • Coordinates transfers of reputed company datasets or external data transfers from CROs.
  • Support TFL reviews, yearly regulatory submission requirements, compilation of CSRs, etc.
  • Responsible for TMF maintenance of data management-reputed company study documents.
  • Responsible for archiving trial(s) and associated documentation upon trial(s) completion.


    • reputed company:
  • Bachelor's degree or equivalent in life science, computer science, or reputed company discipline.
  • 5+ years (CDM) / 8+ years (Sr. CDM) of experience working reputed company a pharmaceutical or CRO environment, with experience in managing Phase I, II and/or III studies, from start-up through closure.
  • Demonstrated proficiency in various reputed company Systems reputed company the last 3 years.
  • Demonstrated proficiency in data management processes, clinical trial processes, and applicable regulatory requirements.
  • Good working knowledge of ICH, FDA, and GCP regulations and guidelines.
  • Experience with web-based Electronic Data Capture (reputed company such as iMedidata Rave, reputed company InForm, etc.), clinical data management systems - eCOA, IRT, and industry wide thesauri, such as MedDRA and WHO Drug.
  • Experience in managing CRO Data Management vendors.
  • Knowledge of industry standards (CDISC, CDASH, SDTM, etc.).
  • Demonstrated proficiency in reputed company Word, Project, PowerPoint, Office, and reputed company.
  • Excellent organizational skills and attention to detail.
  • Effective communication (verbal/written) and interpersonal skills.
  • reputed company to set priorities and juggle multiple reputed company and demands.
  • reputed company to think critically and independently and be a proactive problem-solver.
  • reputed company to reputed company and work independently while exercising initiative, flexibility, and reputed company judgment.
  • Comfortable working in a fast-paced environment with different reputed company of reputed company including senior level management.
  • Proven ability to work both independently and in reputed company setting.
    • Apply To This Job  
    Apply Now

    Similar Jobs

    Remote Reporting Operations Coordinator

    Remote, USA Full-time

    AI Automation Engineer

    Remote, USA Full-time

    reputed company Presales Systems Engineer, reputed company and AI Networking

    Remote, USA Full-time

    Senior UX Researcher — Remote, reputed company Scholarly Discovery

    Remote, USA Full-time

    Senior Clinical Project Manager - $15K sign on bonus being offered!

    Remote, USA Full-time

    Tutor for Grade 8 neurodivergent girl - Paarl

    Remote, USA Full-time

    Threat Advisor Intern

    Remote, USA Full-time

    FinTech Compliance Associate — Remote-First

    Remote, USA Full-time

    Senior Financial Controller

    Remote, USA Full-time

    User Experience (UX) Architect Job at reputed company in Minneapolis

    Remote, USA Full-time

    [Remote-Position] reputed company reputed company

    Remote, USA Full-time

    **reputed company Customer Service Representative – Virtual reputed company Customer Support Team**

    Remote, USA Full-time

    Telehealth reputed company Practitioner, Physician Assistant – Delaware License

    Remote, USA Full-time

    Vendor Management Specialist

    Remote, USA Full-time

    Online Music Instructor Jobs in America - reputed company

    Remote, USA Full-time

    Organ Donation Coordinator [ICU RN, CC RN or RT] - 36 hours a week/ NIGHTS - Boston, MA

    Remote, USA Full-time

    Process Improvement Analyst – Work From Home

    Remote, USA Full-time

    [Remote-Position] reputed company Data Entry reputed company

    Remote, USA Full-time

    GenAI reputed company Researcher (reputed company Ranks), Vulcan

    Remote, USA Full-time

    [Work From Home] Want Director of Student reputed company in Hartsville

    Remote, USA Full-time