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Company Description Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronge…
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Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedica…
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedica…
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 dri…
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 dri…
Company Description We are the company that cares - for our staff, our clients, our partners, and the quality of the work we do. Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with m…
Company Description We are the company that cares — for our staff, our clients, our partners, and the quality of the work we do. Founded in 1995, PSI CRO is a privately owned, global contract research organization with m…
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Company Description PSI is a leading Contract Research Organisation with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on deliveri…
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Full-time
bachelor degree
Global exposure, Career development opportunities, Supportive team culture
Posted 4h ago
~40 hrs/week
Responsibilities
The Legal Counsel will provide strategic legal support across multiple jurisdictions, focusing on clinical trial contract negotiation and healthcare compliance. They will also conduct legal research, monitor legislative changes, and provide risk assessments to internal stakeholders.
Requirements
Candidates must have at least 5 years of legal experience, including 2 years in the pharmaceutical or clinical research industry. A law degree from a recognized university in Croatia and fluency in English are required.
Full job description
Company Description
We are a fast-growing Site Enabling Organization operating globally in the field of clinical research. We are driven by quality, teamwork, and innovation. As we continue to expand our global operations, we are seeking a passionate and dedicated Legal Counsel to join our international Legal Team.
Job Description
As Legal Counsel, you will provide strategic and hands-on legal support across multiple jurisdictions, focusing on clinical trial contract negotiation, healthcare compliance, data protection, employment and corporate matters. You will work closely with our global teams and local stakeholders to ensure legal compliance, risk mitigation, and efficient contract execution. You will report directly to a dynamic and collaborative Global Legal Manager and become a valued team member contributing to our growth and global mission.
Key Responsibilities:
Conduct legal research and due diligence on regulatory and business environments in new and existing markets
Draft, review, and negotiate a broad range of contracts, including:
Clinical trial site agreements (with hospitals, clinics, research institutions)
Services agreements with pharmaceutical sponsors
Employment contracts
B2B/freelance services agreements
Monitor local and global legislative changes relevant to clinical research and business operations
Provide legal risk assessments and guidance to internal stakeholders
Ensure all legal documents meet internal quality and formatting standards (Word/PDF)
Work in alignment with global legal policies and applicable regulatory requirements
Qualifications
Minimum 5 years of experience working as a legal professional, including at least 2 years in a pharmaceutical company, hospital, Site Management Organization (SMO), or Contract Research Organization (CRO) (international/global environment required)
Proven experience in local and international legal matters, including contract drafting and negotiation across jurisdictions;
Strong knowledge of pharmaceutical/clinical research regulations and data protection laws;
Demonstrated ability to work cross-functionally in a multicultural environment and support international business operations.
Law degree from a recognized university in Croatia (international studies such as master degree is a bonus);
Qualified Lawyer in Croatia (preferred but not mandatory)
Fluent in English (minimum C1 level, strong legal English proficiency is a must)
Advanced MS Word and PDF document formatting skills
The ideal candidiate will be :
Proactive and accountable – takes ownership of tasks, follows through on commitments, and demonstrates initiative in identifying and resolving issues.
Confident communicator – able to communicate ideas clearly and assertively while remaining respectful, collaborative, and open to different perspectives.
Passionate about legal work – genuinely interested in legal research, drafting, and maintaining high-quality documentation, with a strong attention to detail.
Collaborative team player – builds effective working relationships with colleagues across functions, cultures, and time zones, contributing positively to an international team environment.
Strong work ethic – thrives in a fast-paced global environment, manages competing priorities effectively, and is committed to delivering high-quality work under demanding workloads.
Additional Information
We Offer:
The opportunity to be part of a rapidly growing and mission-driven international organization
A collaborative and supportive team culture
Global exposure and diverse, high-impact projects
Long-term career development opportunities
How to Apply:
Please submit your CV in English along with a short cover letter highlighting your relevant experience and motivation for joining our legal team.
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines.
PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world.
PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees.
http://www.psi-cro.com
Offices: Baarerstrasse 113a, Zug, 6300, CH
Number One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines.
PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world.
PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees.
http://www.psi-cro.com
Offices: Baarerstrasse 113a, Zug, 6300, CH
Number One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3