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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.

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.

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

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.

VP Global Clinical Trial Management. Vice President, Global Clinical Trial Management. This has been driven by the successful delivery of clinical trials of the highest standards, through their people, innovation and transparency.

Project Coordinators and Clinical Trial Managers to ensure operational excellence. Neuroscience PhD Clinical Trial Coordinator. Clinical Trial Management (CTM).

Assist in training Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs). As a P22 level Clinical Trial Manager, you will oversee the development, coordination, and implementation of Phase I‑IV studies, ensuring milestones, budgets, and regulatory compliance while co

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 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

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 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

Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials or other human sample acquisition projects. We are seeking a professional with working knowledge of clinical trials and clinical databases. Prior ex

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

A leading clinical recruitment firm in the UK is seeking a Clinical Trial Manager to lead the design and execution of global studies for the Renal Denervation portfolio. This fully remote position requires extensive experience in clinical trial operations and regulatory knowledge, as well as fluency

Responsibilities will include: education of patients, families, and colleagues; coordination of the care of patients on trials; collection and preparation of biological samples; collection of trial data; monitoring of expected and unexpected side effects of drugs and other treatment modalities; deve

Senior Sales Representative/ BDM – Clinical Trial Services. Outsourced scientific or operational services supporting clinical trials. This role is responsible for generating new business and developing existing client relationships across biotechnology and pharmaceutical organisations involved in

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 Lang

Impact and Contribution Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Assist in training for Clinical Trials Management Associates (CTMAs) and

Parexel International is seeking an experienced Clinical Trial Manager (CTM) to join their team in the UK, dedicated to managing individual clinical trials. Candidates should have at least 5 years of experience in clinical studies and a Bachelor's or nursing degree. Preferably, candidates will have

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.

Be part of a high-growth organisation where your work directly supports clinical trials and patient outcomes. Sourcing Director OR Sourcing Manager - Clinical Trial Supplies. Director of Clinical Supplies / Supply Chain Director / Head of Purchasing / Comparator Sourcing / Sourcing Manager / Senior

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

This full-time role involves being an internal and external SME for clinical trial design and statistical consultancy for clients. You will work with innovative statisticians, engage with clients, and oversee the application of statistical methods, contributing to the development of cutting-edge tri

The role is responsible for providing advanced expertise in feasibility and site intelligence processes to inform clinical trial planning and execution across the Jazz clinical trial portfolio. Subject matter expert in oncology global clinical trial feasibility and site intelligence to support opera

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.

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

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.

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. Provide end‑to‑end operational leadership for complex, multi‑regional clinical trials fro

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

Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role. Exposure to multiple complex therapeutic areas and global clinical trial operations. Strong understanding of clinical trial documentation, TMF management and regulatory processes.

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Ensures compliance of clinical trials with national and international regulatory requirements and co‑monitors the assigned

Impact and Contribution: Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Core Focus: Overseeing the development and coordination of Phase I-IV c

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. Candidates should expect to have an

A leading biopharmaceutical solutions organization is seeking a Clinical Trial Manager to oversee Phase III studies across Europe. Responsibilities include coordinating clinical research, ensuring compliance with regulations, and supporting teams to achieve project goals.

Provide cross‑cover for other research nurses, trial practitioners, data managers and assistants working in the clinical trials unit as directed by the Clinical Trials Manager. The post holder will take responsibility for the co‑ordination and management of a clinical research portfolio comprisi

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. Clinical Trial Management team. Communicate and collaborate on global study activities; working closely with the project

Support the Principal Pharmacist for Clinical Trials in the provision and development of the clinical trials service, ensuring that all regulatory requirements for Investigational Medicinal Products (IMPs) are met. The successful applicant should have experience working in clinical trials, including

Clinical Trial Associate ManagerLocation: LondonAbout the Role**The Clinical Trial Associate Manager plays a key leadership role in ensuring the successful execution of clinical trials by overseeing a team of Clinical Trial Associates (CTAs). Clinical Trial Associate Manager page is loaded##

A prominent health communications agency in Greater London seeks an experienced Account Manager to oversee day-to-day client management and ensure effective delivery of projects.The ideal candidate will have a strong background in healthcare accounts, exceptional communication skills, and the abilit

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. Clinical Trial Management team. Compile and maintain project-specific status reports within the clinical trial managemen

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

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

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

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