Spineart
Compliance Administrative Assistant
Plan les Ouates
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hirly's read of this role
- Seniority
- Mid level
- Country
- CH
- Work mode
- On-site / unstated
- First seen by hirly
- 16 Sept 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
- Are you passionate about maintaining the highest standards of compliance and administrative excellence?
- Do you want to join an innovative medical device company where you will play a key role in supporting regulatory processes, ensuring documentation accuracy, and upholding our commitment to integrity?
If yes, come to join our legal team!
As Compliance Administrative Assistant
You will provide administrative support to the Legal & Compliance department in all activities related to interactions with Healthcare Professionals (HCPs), including contracts, transparency reporting, and other compliance-related requirements.
Your main responsibilities will be:
Contract management
Prepare, track, and archive contracts, including consultant agreements, Non-Disclosure Agreements (NDAs), sponsorships, hospitality agreements, grants, and other related documents.
Review supporting documentation for completeness and accuracy prior to approval.
Follow up on contract execution and signature processes.
Transparency and compliance
Prepare and submit regulatory disclosures and filings (CNOM, EPS, MDEON, Transparency reporting, etc.).
Collect and maintain information required to meet transparency reporting obligations.
Monitor and track compliance-related files to ensure completeness and timely processing.
Systems Management
Enter, update, and maintain contract and Third-Party information within the Contract Lifecycle Management (CLM) system.
Administrative Support
Manage the Legal & Compliance and Grants shared mailboxes.
Organize meetings, take meeting notes, and draft meeting minutes.
Provide general administrative support to the Compliance team.
Your profile:
2 to 5 years of experience in an administrative support role, preferably within the medical device, pharmaceutical, healthcare, or other regulated industries.
Advanced proficiency in Microsoft Office applications;
Experience with a Contract Lifecycle Management (CLM) system is highly desirable.
Fluent in French and English, with excellent written and verbal communication skills.
Proficiency in one or more additional European languages is a plus.
Excellent organizational and follow-up skills.
Strong attention to detail and commitment to accuracy.
Proactive mindset and ability to adapt to changing priorities.
Reliable and able to manage responsibilities effectively.
Professional discretion and strong respect for confidentiality.
Ability to work independently as well as collaboratively within a team.
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