Healthcare Regulatory Associate Job at Douglas Scott (Greater Manchester)

Healthcare Regulatory Associate

My client is a national top tier law firm, and they are looking to recruit a Hea...

Location

United Kingdom , Birmingham

Salary:

59000.00 - 68000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

Requirements

3–8 years PQE
experience in healthcare regulatory law, including advocacy
a proactive, client-focused approach

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

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

Healthcare Regulatory Senior Associate

My client is a national top tier law firm, and they are looking to recruit a Hea...

Location

United Kingdom , Birmingham

Salary:

75000.00 - 90000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

Requirements

8+ years PQE
Experience in healthcare regulatory law, including advocacy
A proactive, client-focused approach

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

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

Regulatory Associate

The Regulatory team handles a broad range of matters, including healthcare, prof...

Location

United Kingdom , Manchester

Salary:

55000.00 - 65000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

Requirements

Qualified solicitor with 1-5 years' PQE
Previous experience in one or more Regulatory areas

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

Flexible/hybrid working
10% bonus
Highly competitive pension scheme
Private medical cover
Life insurance
Travel insurance

Fulltime

Healthcare Regulatory Solicitor

Join a standout Top Tier law firm seeking Solicitors for their Healthcare Regula...

Location

United Kingdom , London

Salary:

68000.00 - 95000.00 GBP / Year

Douglas Scott

Expiration Date

Until further notice

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

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

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

Associate Copywriter

We are looking for an Associate Copywriter (ACW) to join our growing creative te...

Location

United States , New York

Salary:

60000.00 - 65000.00 USD / Year

Inizio Evoke

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a science-related field (e.g., biology, psychology, chemistry)
OR Significant employment experience in a science-related field requiring familiarity and comfort with scientific publications
Familiarity with reading and interpreting clinical literature
Comfortable working in Microsoft Word and Adobe Acrobat
Excellent attention to detail, grammar, and written communication
Experience supporting annotation, claims, or fact-checking processes in a healthcare or scientific setting

Job Responsibility

Source, validate, and organize medical/scientific references to support promotional claims across healthcare professional (HCP) and direct-to-patient (DTP) materials
Annotate manuscripts and prepare submission-ready reference materials
Ensure consistency of references and annotations across brands, tactics, and writers
Collaborate with editorial to confirm accuracy from manuscript through layout
Support Reg Ops by delivering properly formatted, client-ready annotation files
Serve as a point of contact for annotation and reference-related questions
Help maintain brand-specific reference libraries and stay aligned with client-specific submission rules (e.g., Gilead requirements)
Review and flag unsupported or inconsistent claims proactively
Participate in internal project reviews to stay aligned with creative and strategic direction

What we offer

Fully remote work environment
Company-paid medical
Company-paid dental
401(k)
Tuition reimbursement
Flexible time off

Fulltime

Clinical Trial Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

South Korea , Seoul

Salary:

Not provided

iconplc

Expiration Date

Until further notice

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

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

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

Associate Creative Director, Copy

We are looking for an Associate Creative Director (Copy) who is a master of lang...

Location

United States , Cary; New York; Philadelphia

Salary:

125000.00 - 175000.00 USD / Year

Inizio Evoke

Expiration Date

Until further notice

Requirements

Master of language, storytelling, and strategic communication
Passionate about translating complex scientific and medical information into compelling narratives
Excel at developing writers to deliver impactful, high-quality content
Proven ability to craft impactful and compliant messaging across multiple channels
Inspiring leader and mentor, passionate about fostering talent and guiding teams
Strategic thinker, who understands how copy influences brand positioning, engagement, and behavior change
Highly skilled in adapting tone and voice, writing across various audiences, including healthcare professionals, patients, and caregivers
Meticulous editor, ensuring clarity, accuracy, and alignment with regulatory and brand guidelines
Collaborative partner, who enjoys working with designers, strategists, and account leads
Continuous learner, staying updated on industry trends, regulations, and best practices

Job Responsibility

Be the brand voice expert, ensuring consistency and effectiveness across all written materials
Mentor a team of Copywriters and Senior Copywriters, developing their writing skills and strategic thinking
Create and refine messaging strategies, creating compelling and approvable copy that aligns with brand positioning and market insights
Collaborate closely with Art, Strategy, and Medical teams, integrating copy seamlessly with visual storytelling
Oversee the development of messaging platforms, ensuring consistency across digital, print, social, and video
Navigate and apply regulatory requirements, ensuring all copy is compliant while maintaining creative excellence
Present and defend creative work to clients, regulatory teams, and internal stakeholders
Stay ahead of industry trends, continuously evolving brand messaging to remain relevant and engaging

What we offer

Fully remote work environment
Competitive compensation
Company-paid medical
Company-paid dental
401(k)
Tuition reimbursement
Flexible time off

Associate Counsel

Help drive Big Health’s growth by providing practical, business-minded legal sup...

Location

United States

Salary:

125000.00 - 145000.00 USD / Year

Big Health

Expiration Date

Until further notice

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

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

generous vacation policy
professional development fund
flexible working arrangements
stock options

Fulltime

Healthcare Regulatory Associate

Douglas Scott

Location:
United Kingdom , Greater Manchester

Category:
Legal

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 26, 2025

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