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About Turing: Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L. Role Overview: Turing invites Healthcare and FDA Regulatory Law experts to join projects that fine-tune AI models like ChatGPT. You will apply your expertise in healthcare compliance, FDA drug/device approval, Anti-Kickback Statute analysis, and HIPAA enforcement to evaluate how AI handles healthcare regulatory scenarios. If you enjoy analyzing Stark Law exceptions, False Claims Act liability, and pre-market approval pathways, this is your opportunity. No prior AI experience is required — your background in U.S. healthcare law is exactly what’s needed. What Does Day-to-Day Look Like: • Review and evaluate AI-generated responses to U.S. healthcare law hypotheticals, including HIPAA privacy and security rules, Anti-Kickback Statute safe harbors, Stark Law exceptions, and FDA approval pathways (510(k), PMA, NDA)., • Apply a structured legal rubric to assess issue spotting, accuracy of healthcare regulations, and proper application of CMS guidance and FDA rules., • Identify gaps in AI reasoning around fraud and abuse compliance, clinical trial regulations, telehealth law, and pharmacy benefit management., • Provide detailed, high-quality annotations and written feedback to refine AI models., • Collaborate with researchers and project managers to align evaluation standards and project goals. Requirements: • Juris Doctor (J.D.) from an accredited U.S. law school; Bar admission (active/inactive)., • 3+ years of U.S. legal practice in healthcare law, FDA regulatory affairs, or healthcare compliance., • Strong reasoning skills across HIPAA, the Anti-Kickback Statute, Stark Law, False Claims Act, and FDA regulations., • Excellent written communication and attention to detail., • High ethical standards; interest in AI is a plus. Perks of Freelancing with Turing: • Opportunity to work on cutting-edge AI projects with leading LLM companies., • Competitive compensation., • Flexible, fully remote work arrangement., • Learn how to use AI to advance the legal field. Offer Details: • Commitment: Flexible, 10–30 hrs/week., • Duration: ~1 month, with the possibility of extension based on performance and project needs. After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile. Know amazing talent? Refer them at ___, and earn money from your network.

I’m currently instructed on a standout fully remote Clinical Negligence Solicitor opportunity with one of the country’s leading law firms, renowned for its top-tier Health Litigation practice and genuinely progressive, people-first culture. This is a rare chance to join a market-leading team while benefiting from true flexibility,offering fully remote working without any compromise on the quality of work, support, or long-term career progression. The firm has been recognised as a Top Ten Employer for Working Families 2025 for the second consecutive year, underlining its commitment to flexible working, wellbeing, and sustainable legal careers. The Team You will join a nationally recognised Health Litigation team acting on behalf of NHS Resolution, NHS Trusts and other major healthcare providers. The team is widely respected across the market and is particularly known for its expertise in: • Obstetric and neonatal claims, • Complex, high-value brain injury litigation, • Maternity and patient safety matters The Role You will manage your own caseload of defendant clinical negligence matters from inception through to resolution, with the flexibility to work entirely remotely. Key responsibilities include: • Analysing evidence and conducting investigations, • Drafting detailed advice and reports, • Interviewing witnesses and preparing statements, • Instructing experts and Counsel, • Attending CMCs, hearings and conferences (remotely, with occasional attendance where required), • Negotiating settlements, • Preparing cases for trial and ADR You will also: • Mentor and support junior colleagues, • Assist on complex and high-value claims, • Build and maintain strong client relationships, • Deliver client training and presentations, • Contribute to thought leadership and publications, • Support business development initiatives, • Play a role in continuous improvement within the Health practice, • Have opportunities for client secondments About You This role will suit a solicitor who thrives in a flexible, remote-first environment and is confident managing defendant clinical negligence work independently. You will ideally demonstrate: • Experience handling clinical negligence claims (NHS Resolution or MDO exposure desirable), • Familiarity with the Early Notification Scheme and maternity claims, or a strong interest in specialising in this area, • The ability to work autonomously while remaining highly collaborative, • Strong understanding of client KPIs and reporting requirements, • A proactive, pragmatic and quality-driven approach, • Excellent organisational and communication skills, • Experience mentoring or supervising junior lawyers, • A consistent record of meeting billing and performance targets, • High standards of confidentiality and data security awareness Why Consider This Firm? This firm stands out not only for the quality of its work and reputation in the market, but for its genuine commitment to flexible working,making it one of the few top-tier firms where fully remote working is embedded, supported and sustainable. The benefits package is comprehensive and includes: • 25+ days annual leave, • Annual bonus scheme, • Birthday leave and Christmas shutdown, • Holiday buy/sell and carry over options, • Paid charity and pro bono days, • Optional private medical insurance, • Annual fitness allowance, • Pension and ISA savings schemes with independent financial advice, • Electric and hybrid vehicle scheme, • Health cash plan and Employee Assistance Programme, • Enhanced family leave policies, • Specialist reproductive health and wellbeing support, • Subsidised emergency and back-up care, • Life assurance and income protection, • Bespoke training and development programmes, • Financial support for home working equipment Interested? This is a rare opportunity to join one of the UK’s leading health litigation practices in a role that genuinely delivers on flexibility, career development and work-life balance, without sacrificing the quality, complexity or profile of the work. If you would like to explore this confidentially, including team structure, progression or salary expectations, I would be very happy to discuss. Please apply via the link or contact Rachael Atherton at G2 Legal Recruitment directly.

Medical Negligence Solicitor / Lawyer - Remote The Role This is a fantastic opportunity to join an award-winning law firm that offers specialist quality legal advice to both businesses and individuals nationwide. Due to the development and expansion of the firm’s Clinical Negligence department, it is now seeking to appoint a Solicitor/Legal Executive to take on some excellent cases and work on them from inception to trial. The ideal candidate will have experience handling a caseload of Clinical Negligence claims, investigating and litigating multi-track cases. You must ensure cases are progressed in a timely, efficient and proactive manner and meet all KPI targets set by the firm. This firm currently has a team of experts and are keen to speak to likeminded people, who are passionate about Clinical Negligence and client care. The Candidate • Clinical Negligence Solicitor / Legal Executive handling own caseload (2+ years experience), • Litigation experience (using the DCP), • Experience of drafting legal documentation, • Prioritise and manage a varied caseload, • Ability to work well as part of a team and on your own initiative, • Excellent organisation and time-management skills, • Excellent client care skills The Benefits & How to Apply • Salary, dependent upon experience/PQE - plus an annual bonus, • 35 days annual including bank holidays and Christmas Closure, • Hybrid and flexible working, • Ongoing training and development opportunities, • Social events and charity fundraising days, • Enhanced maternity/paternity pay Apply in the strictest of confidence online and or via telephone – there is no need for a CV for an initial conversation. Contact Roya Ratcliffe Retained Consultant – INDRR Direct Dial: 0161 826 3140 Mobile: 07376 640524

For many, taking part in clinical research offers hope, purpose, and a chance to shape the future of dementia care. But finding the right trial, understanding what it involves, and knowing how to take part can be confusing.

Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs). Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbridge. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbridge.

This full-time, office-based role involves implementing recruitment strategies for clinical research trials, collaborating with Clinical Research Associates, and ensuring effective patient retention. A leading clinical research organization is seeking a Sr Clinical Patient Recruitment Coordinator to

A leading biopharmaceutical solutions organization is looking for a Single Sponsor European Clinical Trial Manager to coordinate Phase III clinical research studies across Europe. The successful candidate will have a bachelor's degree in life sciences or clinical research and experience in managing

A leading dermatology company based in London is seeking a Clinical Trial Associate Manager to ensure successful execution of clinical trials. The role involves overseeing a team of Clinical Trial Associates, ensuring compliance with ICH-GCP and regulatory requirements. Candidates should possess a B

A global healthcare innovator is looking for a Senior Statistician to provide statistical expertise in the design, conduct, analysis, and interpretation of clinical trials. The role requires a master's or doctoral degree in Statistics or a related field and at least three years of relevant experienc

A leading clinical research organization based in London is seeking an Associate Clinical Trial Manager to join their team. This full-time role offers a dynamic work environment and possibilities for career growth in clinical project management. The position includes a comprehensive training period

A leading healthcare communications agency in Greater London is seeking an Account Manager to oversee the management of key client accounts.This position demands excellent verbal and written communication skills, ability to manage multiple projects, and a passion for healthcare.The ideal candidate w

VP Global Clinical Trial Management. Reporting to the Senior Vice President Clinical Operations, you will be a key member of the executive leadership team, leading the Clinical Operations and Project Management functions operationally and strategically. VP Global Clinical Trial Management.

Assist in training Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs). Proficiency with clinical trial management software and tools. As a P22 level Clinical Trial Manager, you will oversee the development, coordination, and implementation of Phase I‑IV studies, e

Clinical Trial Management team. Project Coordinators and Clinical Trial Managers to ensure operational excellence. Associate Clinical Trial Manager (aCTM).

A leading clinical research organization in Greater London is seeking a full-time Associate Clinical Trial Manager to join its Clinical Trial Management team.

A prominent health communications agency in Greater London is seeking an Account Manager to oversee client accounts.The role involves managing creative deliverables, finance oversight, and leading client relationships, requiring strong communication and project management skills.Experience in health

Verbatim Pharma is seeking a Sourcing Director or Sourcing Manager to oversee comparator sourcing for clinical trials. The role requires 4+ years of sourcing experience in clinical trial services, with a focus on unlicensed medicines and parallel imports. Candidates will enjoy autonomy in a fast-pac

A leading health communications agency is seeking an experienced Account Manager to support healthcare campaigns for clinical trials.

Advanced knowledge of Good Clinical Practices (GCP), ISO 14155, and FDA regulations governing clinical trials. R&D Partners is seeking a Clinical Trial Manager to lead the design, planning, execution, and oversight of global clinical studies for the Renal Denervation portfolio. Experience with medic

A pharmaceutical company in the United Kingdom is seeking a Clinical Trial Manager to oversee all aspects of clinical trial management for global studies, ensuring compliance with regulatory standards. The ideal candidate will have a bachelor’s degree in a related field and over 5 years of experie

A leading Clinical Research Organization is seeking a Neuroscience PhD Clinical Trial Coordinator for a full-time role based in the UK. Ideal for PhD graduates looking to enter clinical research, this role involves collaborating on global studies, maintaining project documentation, and ensuring comp

A leading health communications agency in Greater London is seeking an ambitious Account Manager to manage client accounts effectively.This role requires strong verbal and written communication skills and experience managing healthcare accounts.The successful candidate will oversee project delivery,

A leading global pharmaceutical group in the UK is seeking a Clinical Program Lead to manage EU clinical trial programs.

A leading Clinical Research Organisation in London is seeking a Patient Engagement Manager to develop strategies for engaging patients in clinical trials. Ideal candidates will have experience recruiting patients, strong knowledge of clinical trial regulations, and the ability to manage reports and

With at least 5 years of experience in clinical operations and expertise in managing clinical trial documentation, this role offers exposure to innovative cell therapy programs in a hybrid working environment. The candidate will support the operational delivery of Phase I–III clinical trials, ensu

Clinical Trial Management department.

The post holder will take responsibility for the co‑ordination and management of a clinical research portfolio comprising in‑house, national and international phase II and III clinical trials in haematological malignancies. Research Nurse/Clinical Trials Practitioner. The Research Nurse/Clinic

Together, Inclusive and TrialEngine form the only end‑to‑end platform to automate the back office of clinical trials, from pretrial to trial close. Partnerships Manager (Clinical Trial, SaaS, Health tech). Our mission is to enable faster, more successful clinical trials by engineering smart soft

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At La

A leading clinical research organization in London is seeking a Clinical Trial Manager to oversee clinical projects, primarily focusing on Nephrology. Candidates with a passion for clinical trials and at least 5 years of experience in managing such projects are encouraged to apply.

The Senior Clinical Trial Manager, Clinical Operations, serves as the operational lead for assigned early-phase oncology studies, providing end-to-end trial leadership from start‑up through close‑out. Strong knowledge of EU Clinical Trial Regulation (EU CTR 536/2014), ICH‑GCP (E6 R2/R3), GDPR,

Sourcing Director OR Sourcing Manager - Clinical Trial Supplies. Be part of a high-growth organisation where your work directly supports clinical trials and patient outcomes. Are you excited by the idea of building something from the ground up in a fast-growing clinical supplies business?.

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. We believe that people are the most valuable asset of any clinical trial. All materials we create are transl

Harrington Recruitment is seeking a Senior Sales Representative/BDM in the clinical trial services sector. The ideal candidate will have over 6 years of experience in life sciences, with a focus on clinical development.

Associate Director, Clinical Trial Feasibility & Site Intelligence - Oncology,. The role requires a strong ability to integrate data sources and expertise to deliver robust study scenarios, enhancing country and site selection with focused expertise in oncology clinical trials. This position is crit

The Clinical Trial Supply Chain Manager is responsible for overseeing the supply chain and logistics of clinical trial materials to ensure timely and efficient delivery to sites across the globe. Strong knowledge of GCP (Good Clinical Practice), GMP (Good Manufacturing Practice), and regulatory requ

This position offers opportunities to support a variety of clinical trials while working collaboratively in a dynamic team environment.

This full-time role involves being an internal and external SME for clinical trial design and statistical consultancy for clients. A leading clinical research organization in the United Kingdom is seeking a Strategic Statistician to join their Strategic Statistical Services Arm. You will work with i

Candidates should possess a Bachelor's degree in a related field and have 3-4 years of clinical trial experience, particularly in Early Phase studies.

A leading healthcare communications agency is seeking an experienced Account Manager to oversee client services in clinical trial campaigns.

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates. Minimum of 3‑4 years of progressive clinical trial experience. Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable

A leading health communications agency in Greater London seeks an experienced Account Manager to oversee campaigns for clinical trial recruitment.

A leading life sciences company in London is seeking a Clinical Trial Manager to oversee the development and execution of Phase III clinical studies across Europe. The role requires strong project management and organizational skills, as well as familiarity with clinical trial management software.

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. All materials we create are translated and rolled‑out in each country supporting the clinical trial. Langl

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At La

The role involves creating impactful materials for clinical trials aimed at improving lives.