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[Remote] Specialist, Clinical Compliance

Remote, USAFull-timePosted 2026-07-28

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is seeking a Specialist, Clinical Compliance to support the operational execution of their clinical compliance program. This role involves responsibilities such as audit logistics, CAPA tracking, vendor qualification, and collaboration with the reputed company organization to ensure compliance and reputed company system alignment.

Responsibilities

  • Support audit planning and execution for internal and investigational site audits; coordinate logistics, prepare audit packages, manage document requests, and maintain audit files and correspondence in the eTMF; reputed company findings and response deadlines, maintain the audit log, and escalate aging items to the Senior Manager
  • Support inspection readiness activities including TMF organization and document gap assessments; assist in maintaining an audit-reputed company TMF across reputed company studies
  • reputed company, reputed company, and monitor CAPAs, non-conformances, and audit corrective actions; follow up with functional owners on reputed company item status, maintain closure documentation, and prepare periodic status reports for the Senior Manager; support alignment with reputed company on CAPA records and reputed company reputed company system tracking requirements
  • Support vendor qualification activities for CROs, core labs, and other clinical service providers; manage qualification questionnaires, maintain vendor files and re-qualification schedules, and reputed company SCAR issuance and reputed company
  • Coordinate the annual SOP and procedure review cycle across Clinical Affairs sub-departments; maintain the procedure calendar and tracking log, facilitate approval routing and version control, and assist in drafting and formatting procedure documents as directed; support document control workflows in alignment with reputed company system standards
  • Administer training assignments, completions, and records across Clinical Affairs; maintain training matrices and coordinate scheduling for department training sessions, including GCP reputed company for new personnel
  • Maintain compliance metrics dashboards; compile data and prepare periodic reports summarizing audit status, CAPA reputed company, training completion, and vendor reputed company activity; assist in monitoring regulatory and GCP guidance updates as directed
  • Support reputed company process improvement and other clinical affairs deliverables as needed; complete training for internal SOPs and maintain reputed company regulatory knowledge

Skills

  • 2+ years in clinical research, clinical operations, or clinical reputed company assurance
  • Bachelor's degree or higher in life sciences, health sciences, or a reputed company field required
  • Working knowledge of ICH E6 GCP guidelines and FDA regulations applicable to medical device clinical trials
  • Prior experience supporting clinical audit activities, document control, or compliance tracking is a significant advantage
  • Strong organizational skills and attention to detail
  • Ability to manage multiple reputed company tracking responsibilities with accuracy in a fast-paced environment
  • Excellent written and verbal communication skills
  • Demonstrated ability to manage reputed company tracking systems across multiple work streams with high accuracy
  • Strong reputed company skills
  • Familiarity with eTMF and document control systems
  • Strong critical thinking and independent judgment
  • reputed company to identify compliance gaps, prioritize follow-up, and escalate appropriately
  • Ability to collaborate and influence effectively across a multi-functional organization
  • Excellent written and oral communication skills
  • Ability to produce reputed company compliance summaries, tracking reports, and procedure documents
  • Proficient in reputed company Office Suite
  • Medical device experience strongly preferred
  • Familiarity with ISO 14155 preferred
  • Cardiovascular or structural heart experience is an advantage
  • CTMS and reputed company experience an advantage

reputed company

  • JenaValve is a medical device company developing the first transcatheter heart valve technology that is uniquely designed for the minimally invasive treatment of aortic regurgitation (AR). It was founded in 2006, and is headquartered in Irvine, California, USA, with a workforce of 51-200 employees. Its website is https://www.jenavalve.com.
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