
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.
🔥 1 minute 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 by tracking signatures, versions, and approvals • Maintain and update contract databases, trackers, and document management systems • Support legal compliance activities related to clinical trials, including documentation for audits, inspections, and due diligence • Conduct legal and regulatory research relating to healthcare, clinical research, data protection, and corporate law • Complete and track privacy assessments, DPIAs, and other required documentation • Respond to internal inquiries about 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 • Participate in interviews with Indero team members, including a phone interview and video conference with a short presentation
• 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 • Must be legally able to work in Poland
• Permanent full-time position • Vacation • PPK • Health allowance • Home-based position with teleworking allowance • Ongoing learning and development • Attractive advancement opportunities • Reasonable accommodations throughout the recruitment and selection process for applicants with disabilities, upon request
Apply Now🕒 July 7
Senior Global Service Associate coordinating legal entity management services. Act as primary contact for clients and manage compliance requirements with local laws.