Clinical Adviser Job at The Nursing and Midwifery Council (London or Edinburgh)

Clinical Training & Integration Program Coordinator

The Clinical Training & Integration Program Coordinator partners with Executive ...

Location

United States , Oconomowoc, WI

Salary:

Not provided

Rogers Behavioral Health

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
Master’s degree preferred
Previous operational, project management, or program leadership experience required preferably in health care
Knowledge of healthcare agency regulations, such as Joint Commission, State and Federal

Job Responsibility

Lead coordination with Executive Clinical Director of Training Development to manage and oversee clinical training activities
Own the maintenance and integrity of training, review of dashboards, analyzing trends and advising leadership on opportunities for improvement
Develop and execute communication rollout of training updates, expectations, and systemwide initiatives
Serve as a system-level lead and connector, partnering with Talent Development, Clinical Leadership, Marketing, Compliance, IT, and Community Relations
Advise and influence clinical operations, marketing, community relations, quality, and service-line teams to ensure alignment of training and protocol materials
Lead cross-functional alignment efforts to ensure training, protocol updates, and improvement efforts are aligned across departments
Manage project plans, timelines, contributors, and deliverables
Partner with Community Relations, Community Education, and liaison teams to ensure consistency of clinical content when developing or offering external trainings, CEUs, or community presentations
Lead maintenance and lifecycle management of clinical policies, procedures, and compliance with Joint Commission, American Society of Addiction Medicine (ASAM), state licensing, and other regulatory standards
Independently assess regulatory and licensing implications and advise expert clinical leadership

What we offer

Health, dental, and vision insurance coverage for you and your family
401(k) retirement plan
Employee share program
Life/disability insurance
Flex spending accounts
Tuition reimbursement
Health and wellness program
Employee assistance program (EAP)

Fulltime

Medical AI Specialist

We’re looking for a qualified doctor or clinician with AI/ML expertise to join o...

Location

Australia , Melbourne

Salary:

Not provided

Heidi

Expiration Date

Until further notice

Requirements

Clinician with AI product experience
Previous hands-on experience building scalable AI products or features for healthcare settings
LLM & foundation-model expertise
Deep experience with large language models and provider APIs (OpenAI, Claude, Gemini), building LLM-powered healthcare products and features
Prompt engineering & safety
Proven track record crafting, iterating, and testing prompts
mitigating bias and hallucinations
embedding clinical safety guardrails
Cross-functional collaboration
Translate clinical needs into technical specs, partner closely with engineering and product teams, and embed quality controls for clinician trust

Job Responsibility

Own the clinical integrity of Heidi: advise clinicians, troubleshoot edge cases, and validate outputs
Partner with product, engineering and design teams to engineer prompts, build agentic AI, create model evaluation frameworks, and fine-tune models.
Build cutting-edge AI features within Heidi using the latest tools and frameworks
Plan and collaborate on research studies that prove our AI scribe’s clinical accuracy and user impact
Advise leadership on clinical quality and product roadmap priorities
Mentor colleagues and help build a culture of clinical excellence and collaboration

What we offer

Flexible hybrid working environment, with 3 days in the office.
Additional paid day off for your birthday
Special corporate rates at Anytime Fitness in Melbourne, Sydney tbc.
A generous personal development budget of $500 per annum
Learn from some of the best engineers and creatives, joining a diverse team
Become an owner, with shares (equity) in the company, if Heidi wins, we all win
The rare chance to create a global impact as you immerse yourself in one of Australia’s leading healthtech startups
If you have an impact quickly, the opportunity to fast track your startup career!

Fulltime

Legal Counsel

We are seeking an experienced Legal Counsel to support a range of commercial, re...

Location

United States , Westwood

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Juris Doctor (JD) from an accredited law school and active bar membership in at least one U.S. jurisdiction
8+ years of legal experience, with a strong focus on healthcare, life sciences, biotech, or pharmaceutical industries
Proven experience drafting and negotiating complex commercial and clinical agreements within a regulated environment
Deep understanding of healthcare and data privacy regulations, including HIPAA, GDPR, and related frameworks
Experience supporting clinical trials, research agreements, and/or regulatory compliance initiatives
Strong business partnering skills with the ability to communicate complex legal concepts to non-legal stakeholders
Demonstrated ability to work independently in a remote environment and manage multiple priorities effectively
Experience working in-house or through alternative legal service providers (e.g., secondments or consulting engagements) is highly preferred

Job Responsibility

Draft, review, and negotiate a wide range of complex commercial agreements, including clinical trial agreements, master services agreements, licensing agreements, SaaS agreements, NDAs, and vendor contracts
Provide legal guidance on healthcare and life sciences regulatory matters, including compliance with HIPAA, FDA regulations, GDPR, and other applicable data privacy and security laws
Partner with internal stakeholders across R&D, clinical, compliance, and commercial teams to advise on legal risk, contract interpretation, and business strategy
Support clinical trial operations by advising on study agreements, informed consent forms, investigator agreements, and related documentation
Counsel on data privacy, cybersecurity, and data protection matters, including drafting and negotiating data processing agreements and managing incident response
Assist with corporate transactions, including due diligence, M&A support, licensing deals, and strategic partnerships
Manage and liaise with outside counsel, ensuring efficient delivery of legal services and alignment with budget expectations
Develop and implement internal policies, procedures, and training programs related to compliance and legal best practices

What we offer

medical, vision, dental, and life and disability insurance
eligible to enroll in our company 401(k) plan

Clinical Development Veterinarian

Loyal is a clinical-stage veterinary medicine company developing drugs intended ...

Location

United States

Salary:

130000.00 - 160000.00 USD / Year

Loyal

Expiration Date

Until further notice

Requirements

DVM or equivalent degree required
Minimum of 7 years experience, clinical proficiency a must
Excellent verbal and written communication skills to clearly communicate scientific concepts and translate pre-clinical studies into the design and execution of clinical studies
A proven history of collaboration
You have a self-starter mindset and ability to work independently and a commitment to keeping timelines and completion of tasks
A growth mindset that's flexible and adaptive to change in a fast-paced, start up environment

Job Responsibility

Primarily medical monitoring of ongoing clinical trials
Advising our research monitors and clinical operations leaders
Analyzing R&D data to leverage results to execute optimal clinical trials
Mastering protocol and procedures of ongoing clinical trials and contributing to the design and development of new aging drugs for dogs
Serving as subject matter expert, translating veterinary knowledge across R&D, drug development, and clinical operations
Focusing on attention to detail and meticulous record keeping
Upholding GCP standards and following FDA CVM regulations
Occasional travel is required

What we offer

Full-coverage health insurance — medical, dental and vision — for you and your dependents
$1,000 home office equipment stipend
$1,200/year learning budget for books, courses, etc
$250/month wellness budget for gym, cleaners, spa, food, etc
All 3-day weekends are turned into 4-day weekends
Unlimited vacation and paid holidays
Paw-ternity leave — adopt a dog and get a day off with your new family member
Competitive salary
Company equity options grant for new hires

Fulltime

Clinical Negligence Solicitor

Join a leading national firm making a real impact. You will be managing your own...

Location

United Kingdom , Leeds

Salary:

45000.00 - 65000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

Requirements

1yr+ PQE in Medical Negligence
Confident advising clients and handling multi-track cases
Team player with strong attention to detail
Passionate about making a difference

Job Responsibility

Managing your own caseload while assisting on high-value, complex claims – including birth-related brain injuries and spinal cord cases

What we offer

Great holiday package
Flexible and Hybrid working
Working amongst Legal500 recommended Lawyers
Flexible pension & hybrid working
Health cover & digital GP
Paid volunteering days
Ranked in Best Workplaces for Wellbeing 2024

Fulltime

Healthcare Procurement Counsel

Robert Half is supporting a client in the healthcare sector seeking an experienc...

Location

United States , New York

Salary:

85.00 - 110.00 USD / Hour

Robert Half

Expiration Date

Until further notice

Requirements

Juris Doctor (JD) from an accredited law school
Active New York State Bar license (required)
4–8 years of experience drafting and negotiating complex commercial and healthcare‑related contracts, with a strong preference for experience in healthcare, life sciences, health IT, or regulated environments
Demonstrated experience advising on healthcare procurement and vendor agreements, including clinical services, medical technology, digital health, and operational vendors
Strong working knowledge of HIPAA, healthcare data privacy, CMS requirements, FDA‑adjacent considerations, and related regulatory frameworks impacting healthcare contracting
Proven ability to negotiate sophisticated agreements involving technology, services, data use, and compliance‑driven risk allocation
Comfortable operating in a fast‑paced, highly collaborative, stakeholder‑facing environment supporting clinical, operational, and business teams
Experience with public‑sector or quasi‑public procurement environments highly preferred
Excellent written, verbal, and interpersonal communication skills
Ability to operate independently while partnering effectively with senior leadership and cross‑functional teams

Job Responsibility

Provide legal support for healthcare‑related procurements, including: Clinical and operational vendor agreements
Medical devices and healthcare technology
Digital health, telehealth, and data‑driven services
Pharmacy, supply chain, and healthcare operations vendors
Advise business partners on contract structure within regulated healthcare environments
Draft, review, and negotiate a broad range of healthcare‑focused agreements, including: Healthcare IT, SaaS, and cloud‑based platforms
Data‑use, cybersecurity, and interoperability agreements
Professional services, consulting, and clinical support contracts
Advise on healthcare regulatory considerations impacting procurement, including: HIPAA and healthcare data privacy requirements
CMS and reimbursement‑related considerations

What we offer

medical, vision, dental, and life and disability insurance
eligible to enroll in our company 401(k) plan

Senior Medical Director, Late Development, Breast Oncology

This position is for a Senior Medical Director within the atirmociclib program. ...

Location

United States , New York City; La Jolla; Cambridge; Bothell; Groton

Salary:

274500.00 - 444100.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Medical degree with 5+ years of industry experience
Clinical oncology experience (typically 4+ years)
Board certified/eligible in oncology or equivalent preferred
Breast Oncology experience (2+ years)
Ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
Permanent work authorization in the United States

Job Responsibility

Clinical Development Leadership on Study Teams and Development Subteams
Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
Lead peer-to-peer interactions with investigators
Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities
Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional team
Provide clinical development leadership across several study teams
Serve as the Clinical Development Lead on subteams including for Marketing Authorization Applications
Strategic Guidance, Clinical Insights & Interpretation
Collaborate with the Global Development Team to create and refine development strategies
Represent the company in external engagements or as committee member in joint collaborations

What we offer

Participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation support available

Fulltime

Associate Director, Contracts

Beam Therapeutics seeks a business-focused Associate Director, Contracts / Contr...

Location

United States , Cambridge

Salary:

185000.00 - 225000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor's degree required
J.D. strongly preferred
3–7 years of contracts experience in biotech, pharma, or a life sciences or legal department
Demonstrated ability to independently manage the full contract lifecycle, drafting, negotiating, and executing a high-volume, diverse portfolio of agreements including CTAs, MSAs, Research & Collaboration, and Commercial Supply/Manufacturing contracts
Experience supporting Commercial and Medical Affairs functions, with familiarity advising on Advisory Boards, Sponsorships, Grants, and other healthcare-facing engagements
Working knowledge of healthcare compliance frameworks, including HCP engagement practices, fair market value standards, and applicable regulatory requirements
Familiarity with global clinical trial site contracting processes and experience reviewing informed consent forms and related clinical documentation
Hands-on experience with contract lifecycle management (CLM) platforms, with an interest in or track record of contributing to workflow automation, template development, and process improvement initiatives
Ability and enthusiasm for translating complex legal and contracting concepts into accessible training materials and educational sessions for non-legal audiences

Job Responsibility

Draft, review, negotiate, and manage a broad range of agreements, including Clinical Trial Agreements, Master Services Agreements, Consulting, Confidentiality, Research & Collaboration, and Commercial Supply/Manufacturing Agreements
Review and advise on clinical informed consent forms and related documentation
Identify and escalate contractual risks, documentation gaps, and compliance issues with risk-based recommendations
Support compliance contracting processes, including healthcare professional engagement documentation and fair market value validation
Partner with Compliance and cross-functional teams to implement and administer approval workflows supporting Commercial, Legal, and Medical Affairs activities
Provide timely legal support to Commercial and Medical Affairs initiatives (Advisory Boards, Sponsorships, Grants), ensuring alignment with corporate strategy, policy, and regulatory requirements
Advance the company's contract lifecycle management (CLM) systems through workflow refinement, template standardization, automation, and governance improvements
Develop and deliver internal training on contracting processes, templates, and policies
Maintain current and working knowledge of applicable legal and regulatory developments to ensure contracting practices remain aligned with evolving frameworks and industry standards

Fulltime

Clinical Adviser

The Nursing and Midwifery Council

Location:
United Kingdom , London or Edinburgh

Category:
Nursing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
May 04, 2026

Expiration:
May 05, 2026

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