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Innovaderm Research Inc.
Innovaderm Research Inc.
201 – 500 Employees
ConsultingHealthcarePharmaceuticals
Innovaderm Research Inc. is a dermatology-focused Contract Research Organization (CRO) that supports clinical development from Phase I through Phase IV. Since 2000, the company has worked with pharmaceutical and healthcare organizations across North America and Europe, providing study design, regulatory consulting, project management, patient recruitment, and data management for dermatology research.
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Clinical Trial Manager – Europe Remote

Lead clinical sites, CRA oversight, quality, risk, and budgets for dermatology clinical trials at Innovaderm Research. This full-time role is remote across Europe and offered on a six-month contract.

EUEuropean UnionRemoteFull-timeMiddleSeniorEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Manage clinical investigative sites and operational deliverables across clinical trials.
  • Train CRAs and oversee their activities, including transitions between CRAs.
  • Detect site-performance quality issues and trends, then implement corrective action plans.
  • Maintain compliance with study plans, SOPs, ICH/GCP guidance, applicable regulations, laws, timelines, and budgets.
  • Act as the primary sponsor contact for site-level operational matters and clinical deliverables.
  • Support internal, sponsor, and investigator meetings.
  • Conduct risk assessments and oversee mitigation activities.
  • Manage site relationships, training, monitoring performance, screening, and enrollment oversight.
  • Monitor site-visit report metrics and evaluate protocol deviations and related action items.
  • Create Monitoring Plans and support study plans, manuals, reference materials, logs, and site instructions.
  • Deliver CRA training, organize and lead CRA meetings, and conduct quality-assessment and co-monitoring visits.
  • Oversee the development, execution, quality, and completion of SQV, SIV, SMV, and COV activities.
  • Support business development through client meetings, bid defenses, RFPs, and RFIs.
  • Help improve departmental tools and processes.
  • Track, forecast, and reconcile project budgets while supporting change orders and financial planning.
  • Anticipate issues, propose solutions, and help deliver clinical trials on schedule and within budget.
  • Use prior experience to resolve complex issues, develop solutions, and evaluate outcomes.

Requirements

  • Relevant experience and qualifications to carry out the assigned responsibilities.
  • Strong knowledge of the applicable protocol, therapeutic area, and indication.
  • Working knowledge of ICH/GCP guidance, regulations, laws, SOPs, and study-specific requirements.
  • Experience managing clinical monitoring activities and investigative sites.
  • Experience evaluating site performance, monitoring KPIs, audit findings, and corrective action plans.
  • Experience creating monitoring plans and related study plans, manuals, reference materials, logs, and site worksheets or instructions.
  • Experience training, mentoring, and supervising CRAs, Lead CRAs, and clinical operations personnel.
  • Experience overseeing site screening, enrollment, visits, protocol deviations, and risk mitigation.
  • Experience managing clinical-trial budgets, forecasts, reconciliations, billed hours, out-of-scope work, and change orders.
  • A valid work permit for Europe is required.

Benefits

  • Flexible scheduling.
  • Permanent full-time employment.
  • Comprehensive benefits, including medical, dental, and vision coverage, RRSP, vacation, personal days, a virtual medical clinic, public transportation rebates, and social activities.
  • Continuing learning and development opportunities.
  • Opportunities for career advancement.

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