Innovaderm Research Inc.
Innovaderm Research Inc.
Innovaderm Research Inc. त्वचाविज्ञान पर केंद्रित एक कॉन्ट्रैक्ट रिसर्च ऑर्गनाइज़ेशन (CRO) है, जो चरण I से चरण IV तक के क्लिनिकल विकास में सहयोग करता है। वर्ष 2000 से, कंपनी उत्तर अमेरिका और यूरोप में दवा कंपनियों तथा स्वास्थ्य सेवा संगठनों के साथ काम कर रही है और त्वचाविज्ञान संबंधी अनुसंधान के लिए अध्ययन डिज़ाइन, नियामकीय परामर्श, परियोजना प्रबंधन, रोगी भर्ती और डेटा प्रबंधन सेवाएँ प्रदान करती है।

Legal Specialist – Poland (Remote)

Support clinical research contracts, privacy reviews, and compliance activities for Indero’s dermatology and rheumatology CRO operations. Coordinate legal documentation and processes across Poland-based clinical work.

विवरण

  • Provide legal and administrative support for clinical research operations
  • Draft, review, coordinate, and administer CTAs, CDAs, vendor and consultant agreements, amendments, and addenda
  • Manage contract execution by monitoring signatures, document versions, and approvals
  • Keep contract databases, trackers, and document management systems current
  • Assist with clinical-trial compliance records for audits, inspections, and due diligence
  • Research legal and regulatory matters involving healthcare, clinical research, data protection, and corporate law
  • Prepare and monitor privacy assessments, DPIAs, and related documentation
  • Address internal questions about contracts, policies, and legal procedures
  • Create, maintain, and organize legal templates, SOPs, policies, and training resources
  • Work with Clinical Operations, Finance, Procurement, HR, Quality, and other internal teams
  • Coordinate with external lawyers, notaries, and regulatory authorities as needed
  • Safeguard confidentiality and accuracy while maintaining compliance with GCP, privacy laws, and contractual requirements
  • Take part in interviews with Indero team members, including a phone discussion and video conference with a brief presentation

आवश्यकताएँ

  • Paralegal studies diploma, certificate, or comparable legal training
  • At least 3–5 years of experience as a paralegal or legal assistant, ideally in a CRO, pharmaceutical, biotechnology, or other regulated setting
  • Relevant education and professional experience may be considered in different combinations
  • Solid knowledge of contract administration and legal documentation
  • Familiarity with clinical research operations, GCP, and regulatory requirements
  • Highly organized, with careful attention to detail
  • Able to handle competing priorities in a fast-paced, deadline-focused environment
  • Strong written and spoken English communication skills
  • Discreet and professional when working with confidential information
  • Proficient in Microsoft Office and contract or document management systems
  • Legally authorized to work in Poland

लाभ

  • Permanent full-time employment
  • Vacation entitlement
  • PPK
  • Health allowance
  • Home-based work with a teleworking allowance
  • Continued learning and professional development
  • Opportunities for career advancement
  • Reasonable accommodations available throughout recruitment and selection for applicants with disabilities upon request

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