Senior Legal Counsel (EMEA)
Lead SaaS sales contract negotiations and manage day-to-day legal operations within the EMEA region. Provide legal guidance on privacy, employment, and product compliance while supporting cross-functional teams.
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Lead SaaS sales contract negotiations and manage day-to-day legal operations within the EMEA region. Provide legal guidance on privacy, employment, and product compliance while supporting cross-functional teams.
The translator will be responsible for translating and editing specialized content from English into Haitian Creole. They will collaborate with a team to support healthcare and legal sectors.
You will serve as the first in-house legal counsel, taking full ownership of legal matters including commercial contracts, privacy, employment, and intellectual property. You will collaborate across departments to provide practical legal guidance and manage relationships with external specialist counsel.
The Regulatory and Start Up Specialist is responsible for managing site activation readiness, including the preparation and submission of clinical trial applications to regulatory authorities and ethics committees. They also coordinate essential document collection, maintain project trackers, and ensure compliance with international and local regulations throughout the study start-up phase.
The Regulatory and Start Up Specialist is responsible for the timely and high-quality activation of clinical trial sites, including the preparation and submission of regulatory dossiers to authorities and ethics committees. They also manage site-level critical paths, facilitate document translations, and ensure compliance with international and local regulations throughout the study lifecycle.
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The Regulatory and Start Up Specialist serves as the single point of contact for investigative sites and project teams to manage site activation activities. They are responsible for preparing regulatory documents, ensuring adherence to SOPs, and tracking project timelines to ensure successful site initiation.
The consultant will assess and validate the effectiveness of cybersecurity controls against regulatory requirements, security frameworks, and MBSS. They will also manage compliance evidence, support audits, and develop technical reports, dashboards, and policies to ensure ongoing organizational compliance.
The Senior Site Contract Specialist manages the preparation, negotiation, and finalization of investigator contracts while ensuring compliance with legal and financial parameters. They also coordinate with internal teams to align site startup activities and provide mentorship to junior staff.
Negotiate payments with businesses on delinquent accounts, investigate account details, resolve disputes, and use skip tracing to locate debtors. Assess whether accounts should be closed or forwarded to outside counsel while meeting call-volume, service, quality, and productivity expectations.
Provide expert legal counsel and research to support the safe and efficient operation of transportation services. Manage regulatory compliance, assess legal risks, and represent the company through digital channels.
The paralegal will manage front-end legal administration, including answering calls, triaging client enquiries, and maintaining the firm's diary in LEAP. They are also responsible for preparing billing, costs agreements, and court documents while ensuring accurate record-keeping.
The Compliance Analyst will monitor and manage compliance issues while ensuring internal systems meet TISAX and VDA ISA security standards. They will also design audit processes, coordinate reporting channels, and provide technical support for information security controls.
The manager will oversee regulatory and ethics committee submissions across EMEA, Asia Pacific, and Latin America while ensuring compliance with global standards. They will also support business development activities, mentor junior staff, and provide strategic regulatory guidance for clinical trials.
Develop and execute post-approval regulatory submission strategies for CMC activities related to biological and vaccine products. Coordinate cross-departmental efforts to ensure compliance and manage regulatory documentation within information management systems.
The Lead Employment Counsel will serve as the primary legal support for the People team, managing employment matters and external legal relationships. This role involves ensuring global compliance, particularly in the DACH region, and implementing AI tools to streamline legal workflows.
The Regulatory Affairs Consultant will manage post-approval CMC activities, including developing submission strategies and assessing change controls for biological and plasma products. They will coordinate with cross-functional departments to ensure regulatory compliance and maintain documentation within information management systems.
The In-House Legal Counsel Officer serves as the primary internal legal resource, providing support on corporate, commercial, and regulatory matters. Responsibilities include drafting and reviewing contracts, managing regulatory compliance, and advising senior leadership on legal risks and strategic initiatives.
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You will be responsible for the preparation and submission of regulatory documents and CTA packages to ensure compliance with EU CTR and other regional guidelines. Additionally, you will provide leadership for clinical trial start-up activities and serve as the primary point of contact for sponsors and subcontractors.
The Compliance Officer will ensure adherence to AML/CFT regulations, oversee client onboarding, and conduct transaction reviews. They will also monitor regulatory changes, support internal training, and maintain effective compliance frameworks.
The Legal Counsel will manage corporate, contract, and intellectual property matters while providing strategic legal guidance to leadership and product teams. Responsibilities include drafting agreements, enforcing IP rights, and advising on new game features and data protection compliance.
The role involves interpreting global regulations into actionable technical controls and managing compliance across cloud, network, and data environments. You will also lead internal and external audits while partnering with cross-functional teams to maintain a consistent global security posture.
The Regulatory Submission Manager leads operational submission execution for clinical trial applications and acts as the regional regulatory representative within study teams. They are responsible for driving global submission strategies, managing documentation, and ensuring compliance with industry and agency guidelines.
The role involves serving as the legal lead for privacy and AI matters, collaborating with product and engineering teams to embed privacy-by-design and responsible AI principles. You will also draft and negotiate privacy-related contracts and advise on global workforce data issues across various employment products.
The consultant will prepare CMC sections for regulatory submissions and manage lifecycle activities for biologics products. They will also provide technical consulting, coordinate project timelines, and develop regulatory strategies for combination products.
The role involves managing executive calendars, email inboxes, and expense administration while utilizing AI tools to streamline workflows. Additionally, the assistant will draft professional correspondence and maintain accurate administrative reports and dashboards.
The Senior Manager will manage global CMC regulatory support for biological products, including the preparation and review of CTD sections for various regulatory submissions. They will also establish regulatory CMC strategies and coordinate responses to regulatory agencies to ensure timely approvals and compliance.
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The Associate Director leads the promotional material review committee (PMRC) and directs regulatory aspects of internal and external communications for oncology and neuroscience products. They collaborate with cross-functional teams to ensure promotional tactics comply with FDA regulations and company policies.
Provide comprehensive executive and administrative support, including calendar management, meeting coordination, and document preparation. Manage legal and corporate documentation, including intellectual property administration and immigration application support.
The role involves auditing CRM records and sales data to ensure accuracy, completeness, and reconciliation across various systems. You will be responsible for identifying discrepancies, documenting issues, verifying corrections, and preparing daily reports to maintain data integrity.
Translate, post-edit, and review clinical trial documentation to ensure adherence to medical and ethical standards. Collaborate with translation teams to enhance the readability and accuracy of scientific materials while ensuring regulatory compliance.
Stop the endless job search. Our AI finds and applies to the best jobs for you.
We reviewed 10 job postings for remote legal professionals in Romania and found these are the skills employers ask for most often:
| Skill | Share of job posts |
|---|---|
| Regulatory affairs | 70% |
| Regulatory compliance | 70% |
| Stakeholder management | 50% |
| Project management | 50% |
| Site activation | 40% |
| Regulatory Intelligence | 30% |
| Budget negotiation | 30% |
| Communication | 30% |
| Lifecycle management | 20% |
| Pharmacovigilance | 20% |
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