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Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Associate Corporate Counsel, EMEA
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day—enabling our customers to make the world healthier, cleaner, and safer.
The Clinical Trials Division (CTD) of the Pharma Services Group delivers end-to-end supply chain, packaging, comparator sourcing, and logistics solutions to support clinical studies worldwide. With the industry’s largest global footprint of FDA cGMP facilities and strategically located hubs, CTD ensures critical therapies reach patients quickly, reliably, and compliantly.
Key Responsibilities
* Provide practical legal advice on commercial, regulatory, compliance, quality, transportation, and operational issues impacting CTD’s EMEA businesses and global operations.
* Support CTD’s clinical supply operations, transportation, comparator sourcing business by advising on applicable legal frameworks and identifying and mitigating risks.
* Assist in resolving commercial and operational disputes by conducting legal research, gathering facts, preparing analyses, and supporting senior attorneys in negotiations or escalations.
* Contribute to compliance initiatives, including guidance on regulatory requirements such as data privacy, controlled substances, anti-bribery/anti-corruption, competition law, and other areas.
* Partner with cross-functional teams—including Quality, Regulatory, Transportation, Trade Compliance, and Operations—to address issues and advance business objectives.
* Support continuous improvement of policies, legal templates, playbooks, procedures, and review processes to enhance efficiency and alignment with CTD’s business needs and broader legal/compliance functional objective.
* Assist in developing and delivering legal training, communications, and resources to promote compliance awareness and operational excellence.
Qualifications
* Bachelor’s degree and JD / LLB from an accredited law school; licensed and LPC or SQE.
* Established legal practice experience, preferably in-house and in a regulated industry such as life sciences, logistics, pharmaceuticals, healthcare, or clinical trials.
* Experience with regulatory or compliance matters such as pharmaceutical regulations, transportation/logistics requirements, controlled substances, anti-bribery/anti-corruption, competition law, or data privacy.
* Ability to provide practical, business-oriented legal guidance and translate legal concepts into operational solutions.
* Strong written and verbal communication skills, with the ability to collaborate effectively with cross-functional partners in a fast-paced environment.
* Demonstrated analytical, research, and issue-spotting skills with high attention to detail.
* Practical, “doer” mindset with strong judgment and the ability to manage multiple priorities.
* Growth-oriented perspective with a focus on continuous learning, problem-solving, and process improvement.
* Proficient in spoken and written English.
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