Associate - Compliance and Regulatory

Περιγραφή Θέσης

ALG Manousakis Law Firm is seeking an Associate to join its Compliance and Regulatory (Pharma) team. The ideal candidate will have a strong background in pharmaceutical regulatory matters and a passion for advising life sciences clients on complex compliance issues.

Key Responsibilities:

• Advise pharmaceutical and life sciences clients on regulatory compliance matters, including interactions with healthcare professionals (HCPs), healthcare organizations (HCOs), and third-party vendors.
• Ensure compliance with applicable pharmaceutical laws, regulations, and industry codes, including anti-bribery and transparency requirements.
• Interpret and apply pharmaceutical regulations and guidance issued by authorities such as the European Medicines Agency (EMA), national regulatory bodies, and industry associations (e.g., EFPIA Code).
• Provide legal support on product lifecycle matters, including clinical trials, marketing authorizations, labeling, advertising, and pharmacovigilance.
• Draft, review, and negotiate compliance-related documentation, including policies, procedures, and HCP engagement materials.
• Actively participate in client meetings, regulatory authority interactions, and cross-functional compliance projects.

Qualifications:

• A University degree in Law.
• 2 – 5 years’ experience in pharmaceutical regulatory, compliance, or life sciences law, gained at a law firm or as in-house counsel.
• Familiarity with pharmaceutical industry codes of conduct (e.g., EFPIA, IFPMA) and transparency reporting requirements.
• Experience advising on HCP engagements, promotional compliance, or clinical trial regulations.
• Excellent command of the English language; strong written and verbal skills.
• Excellent organization skills; ability to manage multiple projects and conflicting demands.
• Attention to detail, punctuality.
• Ability to build relationships with key clients, co-workers and business partners.
• Collaborative and consultative team player who possesses an ability to work well both independently and in a team environment including with senior management.
• Ability to work comfortably in an intense, fast-paced environment and successfully manage and meet deadlines within a dynamic environment.

Preferred qualifications:

• Experience in drafting and negotiating pharma-related commercial agreements (e.g., clinical trial agreements, licensing, distribution) would be a strong plus.
• Professional proficiency in an additional European language (Italian, Spanish, German, Portuguese, French, etc.) is advantageous.
• Master’s degree (LL.M.) in health law, pharmaceutical law, or a related field is a plus.

We offer:

• Comprehensive private health insurance.
• Competitive salary commensurate with experience.
• Structured training and professional development programs/conferences.
• Direct exposure to multinational pharmaceutical clients and cross-border regulatory matters.
• Clear career progression path within a growing and specialized practice area.