Harvey Nash
Legal Counsel - Life Sciences

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Job Title: Legal Counsel - Life Sciences
Location: Welwyn Garden City (UK) - 3 days a week to office
Duration: 12 months contract
Description:
As Legal Counsel, you will have responsibility for supporting the General Counsel as a key member of the legal team and working with various stakeholders throughout the business, providing sound legal advice across the relevant matters affecting the business.
You will identify and manage commercial and legal risk and work for the creation of sound commercial proposals that meet business areas goals and metrics and protect the Company’s risk levels, reputation and financial interests.
Key Responsibilities:
- Data Protection Operations: Serve as the primary responsible person for operational data privacy matters across the affiliate. This includes managing and resolving Data Subject Requests (DSRs) and investigating privacy incidents, while maintaining a direct reporting line to the Data Protection Officer (DPO) for escalation and strategic alignment.
- Comprehensive Legal Support: Act as a core business partner by advising on UK commercial pharmaceutical laws. Provide comprehensive legal support in the UK and Ireland with a view to ensuring the company achieves its goals and appropriately manages legal risk (to take into account laws and regulations relating to, but not limited to, competition law, commercial, data protection, marketing and advertising, anti-bribery law, litigation and disputes).
- Ethical & Compliance Leadership: Ensuring that the company, employees and agencies operate ethically and in compliance with the company’s Code of Conduct.
- R&D & Clinical Trial Support: Provide proactive legal counsel to global and local R&D teams. This includes advising on clinical trial regulations, reviewing and negotiating clinical trial agreements (CTAs).
- Project & Commercial Execution: Supporting the business to ensure activities are both commercially sound and legally compliant.
- Horizon Scanning & Risk Mitigation: Identify risks and opportunities derived from changes in legislation and ensure that the key legal aspects are taken into account in both planning and decision processes.
- Business Alignment: Ensure alignment and adherence across the relevant business areas in all legal matters.
- Operational Excellence: Ensuring the legal tools, template documents and agreements are maintained and reflect any changes in business practice and relevant laws and regulations.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
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Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
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Who You Are:
- Qualifications: You are a qualified lawyer in England and Wales.
- Core Expertise: You possess a strong, practical knowledge of UK data protection laws (UK GDPR) and UK commercial pharmaceutical law. You are comfortable reviewing and negotiating agreements and providing daily support to diverse business units.
- Industry Experience: Prior experience and knowledge within the life sciences or pharmaceutical industry is required.
- Desirable Competencies: Familiarity or experience with medical device regulations and digital health laws (such as UK Medical Devices Regulations, CE/UKCA marking frameworks, or software-as-a-medical-device guidance) is not mandatory but would be a plus.


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