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