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The Senior Compliance Analyst will manage the company's policy governance framework, conduct regulatory impact assessments, and perform risk-based due diligence. They will also provide business ethics advisory, maintain compliance documentation, and support ESG reporting initiatives.
The Senior Site Contract Specialist manages the end-to-end preparation, negotiation, and finalization of investigator contracts. They collaborate with internal teams and study sites to ensure contractual alignment, risk mitigation, and adherence to project timelines.
The Regulatory and Start Up Specialist is responsible for the timely and high-quality delivery of site activation readiness, including the preparation of clinical trial applications and submission dossiers. They also manage communication with regulatory authorities and ethics committees while maintaining project trackers and ensuring compliance with international and local regulations.
The Regulatory and Start Up Specialist is responsible for the timely and quality delivery of site activation readiness, including the preparation of clinical trial applications and submission dossiers. They also manage communication with competent authorities and ethics committees while maintaining project plans and regulatory intelligence tools.
The Contract Manager is responsible for the full life cycle of sponsor contracts, including drafting budgets, scopes of work, and legal terms. They will collaborate with cross-functional departments to negotiate study budgets and finalize project timelines and costs.
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The role involves managing regulatory compliance, licensing, and reporting across multiple licensed markets. It also requires advising internal teams and monitoring regulatory changes to assess business impact.
The consultant manages regulatory activities and deliverables associated with Clinical Trial Application (CTA) submissions. They lead meetings to align timelines and ensure submissions comply with industry and agency guidelines.
The role involves monitoring compliance with international IT laws and regulations while developing internal policies and procedures. The specialist will conduct audits, assess compliance risks, and prepare reports for internal and external stakeholders.
The role involves supporting the Global Industry Legal Team through legal research on emerging technologies and managing team projects and operations. It also serves as a cross-industry liaison to ensure alignment and consistency across various industry sub-sectors.
Translate and proofread patent-related content from English US into Romanian, specifically within the field of Biology. Ensure the original meaning is conveyed accurately and readably while following specific style guides and CAT tool instructions.
Translate and proofread patent-related content from English US into various European languages, specifically within the field of Biology. Ensure the original meaning is conveyed accurately and is readable for the target audience while following specific style and process instructions.
Perform high-level analysis of complex legal and regulatory filings and provide expert knowledge-based answers for AI research. Validate the professional accuracy of B2B research outputs to improve AI models.
Own and lead the end-to-end security and compliance posture for a global SaaS business. Manage audits and implement security requirements in collaboration with Engineering, Product, and Legal teams.
The Regulatory Affairs Manager will lead the preparation of global clinical trial submissions and provide strategic regulatory guidance to internal and external clients. They are responsible for overseeing multiple projects, managing budgets, and ensuring high-quality regulatory performance across the clinical development lifecycle.
The System Manager, Claims is responsible for the investigation, evaluation, and resolution of complex healthcare-related property and liability claims. This role involves directing legal counsel, negotiating settlements, and establishing financial reserves to protect the organization's interests.
The Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions, ensuring clinical trial documentation complies with regulations. Key tasks include assisting with documentation compilation, tracking timelines, coordinating with IRBs/IECs, and managing document formatting and submission processes.
This role involves continuously monitoring, analyzing, and translating local, regional, and global regulatory developments into actionable insights for regulatory teams and stakeholders. Key duties include conducting impact assessments on regulatory changes and actively engaging in industry forums to inform forward-looking regulatory strategies.
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The Paralegal will work closely with the Legal team to enforce compliance guidelines and assist in monitoring contracting compliance risks. This role also involves acting as a liaison between the Legal and compliance team and implementing digital tools to enhance compliance processes.
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