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Innovaderm Research Inc.
Innovaderm Research Inc.
201 – 500 Darbinieki
Farmaceitiskie produktiKonsultācijasVeselības aprūpe
Innovaderm Research Inc. ir dermatoloģijā specializēta līgumisko klīnisko pētījumu organizācija (CRO), kas atbalsta klīnisko izstrādi no I līdz IV fāzei. Kopš 2000. gada uzņēmums sadarbojas ar farmācijas un veselības aprūpes organizācijām Ziemeļamerikā un Eiropā, nodrošinot dermatoloģijas pētījumu izstrādi, konsultācijas regulējuma jautājumos, projektu vadību, pacientu piesaisti un datu pārvaldību.
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Vakances uzņēmumā

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.

ARArgentīnaAttālinātiPilna slodzeVidējais līmenisVecākais speciālistsNepieciešamā Valoda: angļuAdvokāts
Google Cloud Platform

Apraksts

  • 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.

Prasības

  • 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.

Priekšrocības

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

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