CrawlJobs Logo
Douglas Scott Logo Douglas Scott · Legal

Healthcare Regulatory Associate

United Kingdom, Greater Manchester 45000.00 - 57000.00 GBP / Year · Job Posted April 26, 2025

Job offer has expired

Job Link Share

Job Description

My client are a leading UK defendant firm seeking an experienced Healthcare Regulatory Associate to join their well established national team in Manchester. This is an excellent opportunity to join a dynamic and supportive firm that prides themselves in their commitment to employee wellbeing and a good work life balance.

Job Responsibility

  • Managing your own varied caseload of both advisory and litigation matters
  • Advocacy at inquests, Court of Protection hearings and Tribunals
  • Active involvement in client care and business development

Requirements

  • Managing your own varied caseload of both advisory and litigation matters
  • Advocacy at inquests, Court of Protection hearings and Tribunals
  • Active involvement in client care and business development

What we offer

  • Flexible/hybrid working (minimal office attendance required)
  • Flexible annual leave allowance
  • Performance related bonuses
  • Private medical insurance
Douglas Scott - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Healthcare Regulatory Associate

8 matching positions

Healthcare Regulatory Associate

My client is a national top tier law firm, and they are looking to recruit a Hea...
Location
Location
United Kingdom , Birmingham
Salary
Salary:
59000.00 - 68000.00 GBP / Year
https://www.douglas-scott.co.uk Logo
Douglas Scott
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 3–8 years PQE
  • experience in healthcare regulatory law, including advocacy
  • a proactive, client-focused approach
Job Responsibility
Job Responsibility
  • advocacy at inquests, Court of Protection hearings, and Tribunals
  • advisory work on complex regulatory matters
  • opportunities to get involved in strategic business development initiatives
What we offer
What we offer
  • generous bonus scheme
  • enhanced benefits including private healthcare, enhanced maternity/paternity, 25 days annual leave (with buy/sell options)
  • flexible hybrid working
  • strong support for career progression with direct mentorship from Partners
  • Fulltime
Read More
Arrow Right

Healthcare Regulatory Senior Associate

My client is a national top tier law firm, and they are looking to recruit a Hea...
Location
Location
United Kingdom , Birmingham
Salary
Salary:
75000.00 - 90000.00 GBP / Year
https://www.douglas-scott.co.uk Logo
Douglas Scott
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 8+ years PQE
  • Experience in healthcare regulatory law, including advocacy
  • A proactive, client-focused approach
Job Responsibility
Job Responsibility
  • Advise clients across the health, social care, and education sectors on a broad range of regulatory issues, both contentious and non-contentious
  • Manage a varied caseload that includes advocacy at inquests, Court of Protection hearings, and Tribunals
  • Advisory work on complex regulatory matters
  • Get involved in strategic business development initiatives
  • Supervise Solicitors within the team
What we offer
What we offer
  • Private healthcare
  • Enhanced maternity/paternity
  • 25 days annual leave (with buy/sell options)
  • Generous bonus scheme
  • Flexible hybrid working
  • Strong support for career progression, with direct mentorship from Partners and early responsibility
  • Fulltime
Read More
Arrow Right

Regulatory Associate

The Regulatory team handles a broad range of matters, including healthcare, prof...
Location
Location
United Kingdom , Manchester
Salary
Salary:
55000.00 - 65000.00 GBP / Year
https://www.douglas-scott.co.uk Logo
Douglas Scott
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Qualified solicitor with 1-5 years' PQE
  • Previous experience in one or more Regulatory areas
Job Responsibility
Job Responsibility
  • Handling a broad range of Regulatory matters
  • Healthcare
  • Professional discipline
  • Police investigations
  • Criminal investigations
  • Health, safety & environmental
  • Ofsted & CQC
  • Inquests/public inquiries
What we offer
What we offer
  • Flexible/hybrid working
  • 10% bonus
  • Highly competitive pension scheme
  • Private medical cover
  • Life insurance
  • Travel insurance
  • Fulltime
Read More
Arrow Right

Healthcare Regulatory Solicitor

Join a standout Top Tier law firm seeking Solicitors for their Healthcare Regula...
Location
Location
United Kingdom , London
Salary
Salary:
68000.00 - 95000.00 GBP / Year
https://www.douglas-scott.co.uk Logo
Douglas Scott
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Qualified Solicitors in regulatory/health/social care/education law, join from Solicitor level up to Senior Associate depending on your PQE level
  • Comfortable with both contentious & advisory matters
  • Strong advocate (inquest or Court of Protection experience would be a bonus)
  • Commercially minded with a team-player approach
Job Responsibility
Job Responsibility
  • Handle a rich mix of Court of Protection, inquests, mental health law, CQC/HSE matters, safeguarding, and regulatory litigation
  • Work with public and private sector clients including NHS bodies, local authorities, care providers, and educational institutions
What we offer
What we offer
  • 25+ days holiday (plus buy/sell options)
  • Bonus scheme & private medical cover
  • Pension, life assurance, and more
  • Extensive wellbeing, diversity, and pro bono initiatives
  • Highly competitive salary
  • Remote and Agile working available
  • Fulltime
Read More
Arrow Right

Clinical Trial Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
South Korea , Seoul
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Prior experience or strong interest in clinical research
  • Knowledge of clinical trial processes, regulations, and guidelines
  • Excellent organizational and communication skills
  • Ability to work collaboratively in a fast-paced environment with attention to detail
  • Customs Clearance : Mandatory requirement
Job Responsibility
Job Responsibility
  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions
  • Support the preparation of study-related materials, such as informed consent forms and case report forms
  • Work with cross-functional teams to facilitate communication and ensure smooth trial execution
  • Contribute to the tracking and reporting of clinical trial metrics and milestones
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Associate Counsel

Help drive Big Health’s growth by providing practical, business-minded legal sup...
Location
Location
United States
Salary
Salary:
125000.00 - 145000.00 USD / Year
bighealth.com Logo
Big Health
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • J.D. from an accredited U.S. law school and active membership in good standing with at least one U.S. state bar (California, Massachusetts, or Delaware preferred)
  • 3–5 years of relevant legal experience, ideally with a mix of law firm and in-house in healthcare, digital health, or life sciences
  • Strong experience drafting, reviewing, and negotiating a wide range of commercial contracts
  • Working knowledge of healthcare regulatory frameworks, including FDA regulations for software-based medical devices, HIPAA, and federal and state fraud and abuse laws
  • Familiarity with data privacy and security laws (e.g., HIPAA, GDPR, CCPA) and experience operationalizing privacy compliance
  • Ability to interpret and apply healthcare and data protection regulations in a practical, business-enabling manner
  • Strong written and verbal communication skills, with the ability to translate complex legal concepts and tailor messaging for varied, cross-functional audiences
  • Excellent organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced, high-growth environment
  • Comfort working cross-functionally with product, compliance, commercial, and regulatory teams
  • Proactive, solutions-oriented, and comfortable exercising sound judgment in ambiguous situations
Job Responsibility
Job Responsibility
  • Draft, review, and negotiate a variety of commercial and clinical contracts, including licensing, collaboration, research, and vendor agreements
  • Manage redlines, coordinate with internal stakeholders, and ensure alignment with regulatory, privacy, market access, sales, and other departments’ requirements
  • Maintain and improve contract templates and related policies and procedures to support deal cycles
  • Advise on compliance regarding healthcare regulations (e.g., Anti-Kickback, Sunshine Act, etc.), product claims and advertising, and data privacy laws (US and global)
  • Act as the first point of contact for day-to-day legal questions and translate complex laws into practical guardrails for business teams
  • Contribute to the development of scalable legal workflows and policies
What we offer
What we offer
  • generous vacation policy
  • professional development fund
  • flexible working arrangements
  • stock options
  • Fulltime
Read More
Arrow Right

Corporate Audit Senior Associate

Amgen is seeking a highly motivated and detail-oriented Senior Associate to join...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Accounting, Finance, Business Administration, Compliance, or related field
  • 3–6 years of experience in internal audit, compliance, public accounting, or consulting, preferably in the Pharmaceutical/Biotechnology industry
Job Responsibility
Job Responsibility
  • Audit Planning & Scoping: Participate in walkthroughs and interviews with process owners and business leaders to understand workflows and risk areas
  • Assist in conducting Risk assessment by doing preliminary research to understand relevant business processes, regulatory risks, and internal controls
  • Participate in developing risk-based audit plans (RCM) for functional and U.S. healthcare compliance audits, aligning with corporate objectives and regulatory expectations
  • Assist in defining audit scope, objectives, timelines, and resource requirements in collaboration with Audit Senior Managers and Compliance partners
  • Audit Fieldwork & Reporting: Support execution of audits across various corporate functions (e.g., Finance, Legal, HR, Procurement) and U.S. healthcare operations (e.g., commercial field activities, patient support programs, speaker programs, HCP engagements)
  • Perform detailed testing of transactions, procedures, systems, and controls to assess compliance with Amgen’s policies, SOPs, and relevant laws
  • Support in evaluating adherence to healthcare laws and regulations such as Anti-Kickback Statute, False Claims Act, PhRMA Code and FDA promotional compliance standards
  • Identify audit observations, root causes, and business impacts
  • quantify where applicable
  • Draft audit workpapers and reports in accordance with internal audit methodology & IIA standards
Read More
Arrow Right

Value Access Manager/ Associate Manager

Amgen is hiring a Value Access Manager/Associate Manager in Singapore. The role ...
Location
Location
Singapore , Singapore
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 3-5 years of experience in the pharmaceutical industry
  • At least 2 years working for a global pharmaceutical company in areas of marketing access and/or marketing
  • Good understanding of Singapore Healthcare Systems and future outlook
  • Good understanding of pharma/biotech business model, regulatory and reimbursement processes, compliance guidelines and Health Economics & Outcomes
  • Computer skills (MS Office programs)
  • Fluency in English, both oral and written communications
Job Responsibility
Job Responsibility
  • Developing and leading the implementation of drug access and pricing strategy involving government and private healthcare organizations
  • Work collaboratively with external third-party organizations to align and execute on shared goals across Amgen Singapore’s product portfolios
  • Work cross-functionally to ensure the benefits to patients offered by Amgen products can be optimized
  • Ensure all access initiatives adhere to highest level of integrity and Amgen Values
  • Develop and implement access strategies for responsible portfolios in Singapore, including but not limited to tenders, product listing and patient support program
  • Build long term, substantive relationships with ACE, ALPS and all other relevant stakeholders based on values of trust, respect and transparency
  • Support access to medicines by working with HCOs and HCPs on value-based partnerships to help determine the value of innovation and innovative financing to address access barriers
  • Manage patient support programs in accordance to Amgen SOPs
  • Serve as an internal resource and identify opportunities to maximize HCPs-/HCOs- related projects, and coordinate across functions around key areas of concern for access
  • Provide input and coordination as needed on patient support programs to marketing team to support brand strategy
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right