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Innovaderm Research Inc.
Innovaderm Research Inc.
201 – 500 Angajați
Asistență medicalăConsultanțăProduse farmaceutice
Innovaderm Research Inc. este o organizație de cercetare contractuală (CRO) axată pe dermatologie, care sprijină dezvoltarea clinică din faza I până în faza IV. Din 2000, compania colaborează cu organizații farmaceutice și din domeniul sănătății din America de Nord și Europa, oferind servicii de proiectare a studiilor, consultanță de reglementare, management de proiect, recrutarea pacienților și gestionarea datelor pentru cercetarea dermatologică.
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Legal Specialist – Clinical Research Contracts

Legal Specialist supporting clinical research contracts, privacy assessments, and regulatory documentation. The role coordinates legal workflows with clinical operations and corporate stakeholders.

CACanadaHibridNormă întreagăNivel mediuSeniorLimbă Obligatorie: englezăAvocat
Google Cloud Platform

Descriere

  • Provide legal and administrative support to clinical research operations.
  • Draft, review, coordinate, and administer clinical research agreements, including CTAs, CDAs, vendor and consultant contracts, amendments, and addenda.
  • Manage contract execution processes and monitor signatures, versions, and approvals.
  • Keep contract databases, trackers, and document management systems accurate and up to date.
  • Assist with legal compliance for clinical trials, including audit, inspection, and due-diligence records.
  • Research legal and regulatory matters involving healthcare, clinical research, data protection, and corporate law.
  • Complete and monitor privacy assessments, DPIAs, and supporting documentation.
  • Address internal questions about contracts, policies, and legal procedures.
  • Create, revise, and organize legal templates, SOPs, policies, and training resources.
  • Collaborate with Clinical Operations, Finance, Procurement, HR, Quality, external counsel, notaries, and regulatory authorities.
  • Protect confidentiality and maintain accuracy and compliance with GCP, privacy laws, and contractual requirements.

Cerințe

  • Diploma or certificate in paralegal studies or equivalent legal training.
  • At least 3–5 years of experience as a paralegal or legal assistant, preferably within a CRO, pharmaceutical, biotech, or other regulated environment.
  • Equivalent combinations of relevant education and professional experience will be considered.
  • Strong knowledge of contract administration and legal documentation.
  • Familiarity with clinical research operations, GCP, and applicable regulatory frameworks.
  • Excellent organization and close attention to detail.
  • Capacity to manage competing priorities in a fast-paced, deadline-oriented setting.
  • Strong written and verbal communication skills in English.
  • Discretion and professionalism when managing confidential information.
  • Proficiency with Microsoft Office and contract or document management systems.
  • Legal authorization to work in Canada.

Beneficii

  • Flexible working hours
  • Permanent full-time employment
  • Comprehensive benefits package including medical, dental, vision, RRSP, vacation, personal days, virtual medical care, public transit rebates, and social activities
  • Ongoing professional learning and development opportunities

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