Innovaderm Research Inc.
Innovaderm Research Inc.
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.

Legal Specialist – Argentina (Remote)

Provide legal support for clinical research contracts, privacy assessments, and compliance at Indero, a dermatology and rheumatology CRO. This home-based Argentina role coordinates legal documentation with clinical operations.

Descriere

  • Provide legal and administrative support to the Legal Department for 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 by tracking signatures, document versions, and approvals.
  • Keep contract databases, tracking tools, and document management systems current.
  • Prepare and maintain legal compliance documentation for clinical-trial audits, inspections, and due diligence.
  • Research legal and regulatory matters involving healthcare, clinical research, data protection, and corporate law.
  • Complete and monitor privacy assessments, DPIAs, and other required records.
  • Address internal questions about contracts, policies, and legal procedures.
  • Create, revise, and organize legal templates, SOPs, policies, and training resources.
  • Work with Clinical Operations, Finance, Procurement, HR, Quality, and other internal teams.
  • Coordinate with external counsel, notaries, and regulatory authorities as needed.
  • 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 setting.
  • Relevant combinations of education and professional experience will also be considered.
  • Solid knowledge of contract administration and legal documentation.
  • Familiarity with clinical research operations, GCP, and regulatory frameworks.
  • Highly organized, with careful attention to detail.
  • Able to manage competing priorities in a fast-paced, deadline-driven environment.
  • Strong written and verbal English communication skills.
  • Discreet and professional when handling confidential information.
  • Proficient with Microsoft Office and contract or document management systems.
  • Legally authorized to work in Argentina.

Beneficii

  • Flexible work schedule.
  • Home-based position.
  • Ongoing learning and development.
  • Opportunities for career advancement.
  • Stimulating work environment.

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