
201 - 500 employees
💊 Pharmaceuticals
🏥 Healthcare
💼 Consulting
Pharmaceuticals • Healthcare • Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
🔥 12 hours ago
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201 - 500 employees
💊 Pharmaceuticals
🏥 Healthcare
💼 Consulting
Pharmaceuticals • Healthcare • Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
• Support the Legal Department with legal and administrative assistance related to clinical research operations. • Prepare, review, coordinate, and administer clinical research contracts, including CTAs, CDAs, vendor and consultant agreements, amendments, and contract addenda. • Coordinate contract execution workflows, tracking signatures, versions, and approvals. • Maintain and update contract databases, trackers, and document management systems. • Support clinical-trial legal compliance documentation for audits, inspections, and due diligence. • Conduct legal and regulatory research related to healthcare, clinical research, data protection, and corporate law. • Complete and track privacy assessments, DPIAs, and other required documentation. • Respond to internal inquiries regarding contracts, policies, and legal processes. • Develop, update, and organize legal templates, SOPs, policies, and training materials. • Liaise with Clinical Operations, Finance, Procurement, HR, Quality, and other internal stakeholders. • Coordinate with external counsel, notaries, and regulatory bodies when required. • Ensure confidentiality, accuracy, and compliance with GCP, privacy laws, and contractual obligations.
• Diploma or certificate in Paralegal Studies or equivalent legal training. • Minimum of 3–5 years of experience as a paralegal or legal assistant, preferably in a CRO, pharmaceutical, biotech, or regulated environment. • Different combinations of relevant education and work experience will be considered • Strong understanding of contract administration and legal documentation. • Familiarity with clinical research operations, GCP, and regulatory frameworks. • Excellent organizational skills with strong attention to detail. • Ability to manage multiple priorities in a fast-paced, deadline-driven environment. • Strong written and verbal communication skills in English. • High level of discretion and professionalism when handling confidential information. • Proficiency with Microsoft Office and contract/document management systems. • Legally authorized to work in Argentina.
• Flexible work schedule / work schedule • Home-based position • Ongoing learning and development • Attractive advancement opportunities • Stimulating work environment
Apply Now🕒 August 17
Legal Intake Specialist supporting US law firms with Medicaid, estate, asset-protection, and long-term-care inquiries. Conducting empathetic phone intake, qualifying prospects, maintaining CRM records, and scheduling attorney consultations.
🇦🇷 Argentina – Remote
💵 $1.1k - $1.2k / month
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧑💼 Attorney / Lawyer
🚫👨🎓 No degree required
🗣️🇪🇸 Spanish Required