82 Medical Director jobs in the United Kingdom

Medical Director

Greater London, London HUM2N

Posted 14 days ago

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Job Description

Medical Director HUM2N 


Summary


HUM2N is a healthcare brand which is the antidote to mainstream medicine. HUM2N launched in 2020 and currently operates out of a 4500 sq ft state-of-the-art, futuristic lounge in trendy Chelsea, London. At HUM2N, we use biology to understand your past, and cutting-edge science to transform your future. Health has traditionally been defined as “the absence of disease”, with traditional medicine solely focusing on treating symptoms. It’s time for a new era of healthcare. We believe healthcare starts when you’re healthy.


Our mission is to uncover the root causes, and resolve, prevent, and optimise our clients’ health to reach their true potential - no matter where they are on their journey.

We do this through our personalised health programmes delivered by our physician-led team, cutting-edge therapies at our HUM2N Lounge, ongoing health expert support and through our powerful range of medical-grade supplements. The HUM2N lounge offers treatments. In the future, HUM2N will scale the lounges globally and provide B2B products to clinicians that HUM2N will train in our academy.


Minimum Experience

Management & Leadership: 3 years of managing and leading clinical teams in healthcare organisations, inc CQC leadership experience, and service design. 

Clinical Experience: 1 0+ years of direct clinical experience in primary or secondary care , with 5+ years of experience in Functional Medicine. 

Qualifications: CCT in medical speciality egMRCGP, Functional Medicine.

Education: Delivering education to physicians and healthcare teams.

Research : Involvement in design and execution of research, published.


Medical Director

The Medical Director is a senior leadership role responsible for overseeing the medical operations and ensuring the highest standards of care and patient safety within the organization. The Medical Director plays a critical role in shaping clinical policies, driving medical strategy, and ensuring alignment with the organisation's overall goals. They will be supported by the medical board inc Director of Functional Medicine and work closely with the founder and CEO. As we seek to scale the reach of the personalised medicine we are offering. 


Key Responsibilities


Medical Leadership and Strategy

  • Develop and implement the clinic’s overall medical strategy, focusing on longevity, preventative care, and regenerative and functional health in conjunction with Dr Enayat.
  • Establish and update clinical protocols and standard operating procedures (SOPs) to ensure consistency and quality in patient care delivery. Safeguard alignment with the latest advancements in longevity, functional, regenerative medicine, and wellness.
  • Provide clinical oversight for the safe and effective use of clinic therapies
  • Ensure training and development for staff is in place, with clinical performance management 121s and development plans for each client facing practitioner.
  • Develop clinical team leads eg NT, clinic therapies, DC lead, aesthetic lead; and provide a system for them to be able to operate effectively in. 
  • Lead the clinical integration of medicine with clinic based services - aesthetics and therapies to ensure a comprehensive, patient-centred approach.
  • Act as the key communicator of medical objectives to the clinic's board, administrative teams, and external stakeholders, providing strategic insights and updates on clinical performance.


Patient Care and Clinical Excellence

  • Develop and oversee patient care standards, policies and protocols, ensuring they meet the highest standards of safety, effectiveness, and patient satisfaction.
  • Set measurable performance indicators like client recovery times and treatment efficacy/outcome.
  • Conduct client consultations, assessments, and diagnostic evaluations for patients seeking functional and longevity medicine and wellness treatments.
  • Supervise the administration of treatments, particularly high-risk therapies, and ensure they adhere to regulatory standards and best practices.
  • Oversee the clinical team in delivering comprehensive health plans to patients that address root causes of chronic conditions and optimise overall well-being.



 Regulatory Compliance and Quality Assurance (work with Operations) 

  • Provide strategic oversight of clinical operations including practicing privileges and HUM2N health services, delegating day-to-day management to the clinic operations manager and department leads. Maintain oversight of quality assurance projects and audits, ensuring compliance with Care Quality Commission (CQC) standards, GDPR, and other regulatory bodies.
  • Share oversight with the CEO/COO of the CQC registered Manager / Clinical Operations Manager to ensure quality assurance projects and audits are completed as per CQC requirements. 
  • Continuously review patient outcomes and clinical data to refine and improve care protocols.
  • Develop systems to identify and mitigate clinical risks, such as adverse events or breaches of patient confidentiality.


 Team Leadership and Development:

  • Manage and mentor a team of practitioners, including physicians, nutritional therapists, and wellness specialists, ensuring alignment with the clinic's mission and values; and practice privileges team.
  • oversee the onboarding process of health practitioners
  • Provide clinical training to staff on emerging longevity-focused treatments and functional medicine protocols, and oversee training and development plans per practitioner for them to meet their JD with excellence.
  • Foster a culture of continuous learning, clinical excellence, and innovation within the clinic.
  • Establish and govern a framework for the ongoing evaluation for the clinical team.


Practising Privileges Doctors' Management and Governance:

  • Oversee governance protocols for all practising doctors, ensuring they comply with clinic policies, UK medical standards, and continuing education requirements. Implement regular reviews and assessments to ensure the consistent quality of care provided by the medical team.
  • Establish a framework for the ongoing evaluation of practising doctors.
  • Regularly review and renew practising privileges, overseeing the conduction audits by the cqc registered / clinic operations manager to verify ongoing compliance with clinical and ethical standards.
  • Implement robust governance policies to protect the clinic from performance issues, malpractice claims, or non-compliance among practitioners, ensuring patient safety and clinic reputation.
  • Drive referrals into HUM2N services from PP through education, and engagement. 



 Business Development and Collaboration

  • Work closely with the CEO and COO in business development to explore new opportunities for clinic growth, partnerships, and service expansion both in the UK and Internationally.
  • Collaborate with external healthcare providers, insurers, and suppliers to establish partnerships that enhance service offerings and reduce costs.
  • Foster relationships with academic institutions, industry leaders, and research organisations to promote clinical innovation and explore new revenue streams, such as partnerships in clinical research, product development, or industry affiliations.



Medical IT Systems and Data Integration

  • Ensure that data from patient treatments, diagnostics, and wearable health technologies are effectively integrated into clinical practice to support personalised care plans and long-term health monitoring.
  • Collaborate with IT and tech teams to explore emerging health technologies, such as AI-driven diagnostics, telemedicine platforms, and wearable technologies, to improve the clinic’s diagnostic capabilities and patient engagement.
  • Leverage data analytics to monitor clinical performance, patient outcomes, and business metrics, translating insights into actionable strategies.



Educational Initiatives and Events

  • Foster a learning environment by providing education on key wellness topics such as Longevity medicine, functional medicine, and clinic therapies offered at the clinic. 
  • Oversee the development of patient education, including information and instructional materials, webinars, and one-on-one consultations, to enhance patient understanding of their treatment plans and the science behind functional and longevity therapies.
  • Design and implement ongoing training / educational programs.
  • Spearhead community outreach programs, such as health seminars or preventive care workshops, to enhance the clinic's public profile.
  • Driving and measuring medical referral quantity , quality , outcome and revenue.


Industry/ Clinic Representation

  • Represent the clinic at conferences, seminars, and other industry events to promote its vision and services. Represent the clinic’s expertise and leadership in the field of functional medicine and longevity through PR, national and international media outlets, journals and more.
  • Represent the clinic as a speaker at conferences, industry events, and medical symposia focused on functional medicine and HUM2N Methodology, illustrated by evidence collected (case studies, research) . 
  •  In the absence of the CEO, serve as the on-site clinical leader, interacting directly with patients, addressing their concerns, and maintaining the clinic’s operational continuity. Ensure visibility and active engagement with both clients and staff.


 Evidence, Research and Innovation

  • Build body of evidence, case studies, publications, research studies, testimonials. 
  • Lead / collaborate on clinical research initiatives related to longevity, regenerative & functional medicine, and other innovative treatments. Partner with academic institutions, biotech firms, and industry players to develop and implement new treatments that push the boundaries of healthspan and longevity interventions.
  • Ensure that new treatments and protocols introduced in the clinic are based on rigorous scientific evidence and contribute to the field of longevity and wellness.
  • Partner with universities or research institutions to advance medical knowledge and contribute to peer-reviewed publications.









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PV Medical Director

London, London £900 - £1000 Daily SRG

Posted 4 days ago

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Job Description

temporary

PV Medical Director
Temporary role
Remote
circa. (Apply online only) per day

SRG are supporting one of the leading global pharmaceutical companies with their search for a new Medical Director to support the PV/Drug Safety team on a temporary basis. This 6 month contract will be great for a Senior PV or Drug Safety Physician with ample experience in a similar role. You will need to have worked regularly within Safety Evaluation and Risk Management tasks and be able to start at short notice. While not essential, experience within Oncology in particular - will be a great advantage.

Key responsibilities include:

  • Conducting routine pharmacovigilance tasaks including signal detection activities and signal validation/assessment
  • Authoring & reviewing key regulatory documents (e.g. DSURs, EU RMPs and PBRERs) as well as responses to regulatory questions
  • Supporting identification of needs for product labelling updates
  • Driving proactive implementation of risk management initiatives
  • Facilitating safety governance/SRTs in the clinical development (and post marketing) settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address product safety issues
  • Ensuring that adverse event(s) and other safety information is efficiently evaluated and accurate to meet global compliance and regulatory requirements

Skills/Experience needed:

  • Medical degree (e.g. MD, MBBS) - GMC registration strongly preferred
  • Some clinical experience post-registration
  • Experience within the pharmaceutical industry, within Drug safety / PV
  • Therapeutic area experience within Oncology desired
  • case review of adverse events from clinical trials - not case management but Medical review experience required from a safety perspective in clinical trials
  • Specific experience within Safety Evaluation and Risk Management activities
  • Argus drug safety experience or similar drug safety database experience
  • Ability to contribute successfully to teams
  • Strong verbal and written communication skills

If interested, please follow the link to apply or get in touch with Theo Charles to discuss further!

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

This advertiser has chosen not to accept applicants from your region.

PV Medical Director

EC1 London, London SRG

Posted 7 days ago

Job Viewed

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Job Description

temporary

PV Medical Director
Temporary role
Remote
circa. (Apply online only) per day

SRG are supporting one of the leading global pharmaceutical companies with their search for a new Medical Director to support the PV/Drug Safety team on a temporary basis. This 6 month contract will be great for a Senior PV or Drug Safety Physician with ample experience in a similar role. You will need to have worked regularly within Safety Evaluation and Risk Management tasks and be able to start at short notice. While not essential, experience within Oncology in particular - will be a great advantage.

Key responsibilities include:

  • Conducting routine pharmacovigilance tasaks including signal detection activities and signal validation/assessment
  • Authoring & reviewing key regulatory documents (e.g. DSURs, EU RMPs and PBRERs) as well as responses to regulatory questions
  • Supporting identification of needs for product labelling updates
  • Driving proactive implementation of risk management initiatives
  • Facilitating safety governance/SRTs in the clinical development (and post marketing) settings by assisting in the establishment and operation of cross-functional teams in any SERM to detect and address product safety issues
  • Ensuring that adverse event(s) and other safety information is efficiently evaluated and accurate to meet global compliance and regulatory requirements

Skills/Experience needed:

  • Medical degree (e.g. MD, MBBS) - GMC registration strongly preferred
  • Some clinical experience post-registration
  • Experience within the pharmaceutical industry, within Drug safety / PV
  • Therapeutic area experience within Oncology desired
  • case review of adverse events from clinical trials - not case management but Medical review experience required from a safety perspective in clinical trials
  • Specific experience within Safety Evaluation and Risk Management activities
  • Argus drug safety experience or similar drug safety database experience
  • Ability to contribute successfully to teams
  • Strong verbal and written communication skills

If interested, please follow the link to apply or get in touch with Theo Charles to discuss further!

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

This advertiser has chosen not to accept applicants from your region.

Divisional Medical Director

London, London Cygnet

Posted 4 days ago

Job Viewed

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Job Description

Are you a dynamic and visionary clinical leader ready to shape the future of mental health care?


Are you ready to join an award-winning, industry-leading organisation where quality is at the heart of everything we do — and excellence is more than just a word, it's our culture? With just under 300 medical professionals on our team, we’re setting the standard for care.


Cygnet Health Care is seeking an exceptional Divisional Medical Director (DMD) to take on a pivotal executive leadership role. As the most senior medical leader within your division, you will drive the strategic direction, uphold the highest professional standards, and lead a high-performing medical workforce dedicated to delivering safe, effective, and person-centred care.

This is a unique opportunity to collaborate at the highest level across multidisciplinary teams, influence organisational priorities, and champion a culture of innovation, learning, and continuous improvement.


Cygnet distinguishes itself through a unique combination of scale, specialism, and personalisation of care. Our 13,000 staff support 8,300 individuals and with a portfolio of over 150 services, we offer care across a range of services from acute, PICU, Eating Disorders and CAMHS. We have a strong reputation for quality, inclusion, and staff satisfaction. We stand apart through our ability to deliver exceptional, high-acuity care at scale, underpinned by deep clinical understanding, sector-leading quality ratings, and an unwavering focus on person-centred practice.


We keep our focus on maintaining high-quality standards across all our services, consistently achieving sector-leading regulatory ratings across the UK. 81% of services evaluated earned a Good or Outstanding rating by regulators, outperforming the national average. Cygnet has 17% higher CQC Good or Outstanding ratings than the rest of the mental health independent sector and 95% of our hospitals are rated Good or Outstanding by our internal quality assessment team. Our collaboration with 360 commissioning bodies, has not only allowed us to support integrated pathways of care, but has also helped shape local and regional strategies for individuals with complex needs.


Cygnet has also been recognised externally, with recent wins at the HealthInvestor Awards including Specialist Care Provider of the Year and has also been recognised by the Carers Trust, with 20 of our services being awarded Triangle of Care accreditation.


Reporting directly to the Group Clinical Director, this is a full-time position responsible for strategic leadership of our Health Care South region (Including Greater London, South East, South West, South Wales and West Midlands). This is a remote role but will include travel to sites within this region 2 – 3 days per week, so access to a car & UK driving licence is essential.



Key Responsibilities:


Strategic and Clinical Leadership


  • Provide strategic clinical leadership across the division, setting high standards for medical practice and professional conduct.
  • Ensure alignment with national clinical policy and statutory requirements, championing evidence-based care, prevention, early intervention, and integrated models of service delivery.
  • Promote a strong culture of patient safety, learning, and openness in line with Just Culture principles.


Clinical Governance and Quality Improvement


  • Oversee clinical governance frameworks to ensure safe, effective, and person-centered care.
  • Lead on clinical quality improvement, audit, and innovation initiatives, ensuring high standards of care are maintained and continuously enhanced.
  • Promote adherence to policies relating to safeguarding, medicines optimisation, infection prevention and control, and controlled drug safety.


Medical Workforce Leadership


  • Lead on all aspects of clinical workforce planning, including recruitment, retention, role redesign, and succession planning.
  • Ensure a high-performing and appropriately skilled clinical workforce through oversight of appraisal, revalidation, CPD, and professional development.
  • Embed a culture of reflective practice, supervision, and 360-degree feedback within medical leadership.


Operational Excellence and Resource Stewardship


  • Work closely with the respective Managing Directors and regional clinical directors to ensure high-quality and high-value service delivery.
  • Ensure clinical productivity and resource utilisation are optimised, with clear outcome measures and benchmarking in place.
  • Contribute to the achievement of the overall financial targets by the division.


Innovation, Research and Partnership


  • Foster academic and clinical partnerships with external stakeholders, including NHS bodies, academic institutions, and research networks.
  • Promote engagement in ethically approved research, supporting a culture of inquiry, learning, and evidence-based practice.
  • Champion patient and resident involvement in research to inform service development and improve care outcomes.


We are looking for someone who is…


  • Extensively experienced in senior medical leadership, ideally at Associate Medical Director, Regional Medical Director, Divisional Director or equivalent level.
  • Holds an in-depth understanding of clinical and corporate governance frameworks.
  • Has comprehensive knowledge of the professional, educational, and regulatory requirements of the medical workforce.
  • Experienced in service redesign, workforce transformation and strategic planning.
  • Demonstrates a proven ability to lead change, manage complex teams and influence across organisational boundaries.
  • Demonstrates commitment to quality improvement and evidence-based practice in a multi-disciplinary setting.
  • Holds strong financial and budget management skills (desirable).
  • Experienced in medical research, audit, and clinical effectiveness.
  • Shows high emotional intelligence and excellent interpersonal skills, with the ability to navigate complexity and foster consensus.
  • Excellent written, verbal, and presentation skills, with the ability to engage diverse stakeholders.
  • Committed to ongoing personal and professional development, including the use of feedback tools such as MSF/360 appraisal.
  • Fully registered GMC & MBBS (or equivalent) qualified, and registered on the specialist register (CCT/CESR), Section 12 and AC Status


Why Cygnet? We’ll offer you…


  • Market leading salary and bonus
  • Company shares
  • Travel allowance
  • Generous annual leave entitlement that increases with length of service
  • Company paid Life Assurance scheme covering 3x salary
  • Contributory pension scheme
  • Electric Car Scheme
  • Free meals, on-site parking and EAP support
  • Research and teaching opportunities, as well as the opportunity to lead and participate in QI & Audit initiatives
  • A unique opportunity to lead the development of new services within the independent sector, shaping an innovative model of care from the ground up
  • Extensive development opportunities and monthly CPD groups
  • Peer‑led “Characters of Care” programme and a comprehensive employee benefit and support programme
  • Company Funded Cash plan with the ability to claim up to £1000 per annum worth of benefits including free Physiotherapy, Osteopaths, Optical, dental, consultations, scans and free prescriptions
  • Gym Discounts across the UK as well as free online fitness classes with ClassPass, Nutritional Programmes and Fitness Consultations
  • Discount schemes including Reward Gateway, NHS Discount and Blue Lights Card
  • Smart Health Toolkit, including 24 hour GP service with the option of prescription delivery to your local pharmacy


If you would like to discuss this informally we’d be more than happy to facilitate this. Please contact: Hannah Dunlop via or 077 20 497 792


Requirements


The successful candidate will be required to undergo an enhanced DBS and reference check and an offer of employment will be subject to successful clearance.


*Recruitment agencies please note: Speculative emails are not to be sent directly to our clinical staff, these need to go via our internal recruitment team. If speculative candidates are sent directly to a member of the clinical team, we will consider these candidates as our own*

This advertiser has chosen not to accept applicants from your region.

Divisional Medical Director

Cygnet

Posted 4 days ago

Job Viewed

Tap Again To Close

Job Description

Are you a dynamic and visionary clinical leader ready to shape the future of mental health care?


Are you ready to join an award-winning, industry-leading organisation where quality is at the heart of everything we do — and excellence is more than just a word, it's our culture? With just under 300 medical professionals on our team, we’re setting the standard for care.


Cygnet Health Care is seeking an exceptional Divisional Medical Director (DMD) to take on a pivotal executive leadership role. As the most senior medical leader within your division, you will drive the strategic direction, uphold the highest professional standards, and lead a high-performing medical workforce dedicated to delivering safe, effective, and person-centred care.

This is a unique opportunity to collaborate at the highest level across multidisciplinary teams, influence organisational priorities, and champion a culture of innovation, learning, and continuous improvement.


Cygnet distinguishes itself through a unique combination of scale, specialism, and personalisation of care. Our 13,000 staff support 8,300 individuals and with a portfolio of over 150 services, we offer care across a range of services from acute, PICU, Eating Disorders and CAMHS. We have a strong reputation for quality, inclusion, and staff satisfaction. We stand apart through our ability to deliver exceptional, high-acuity care at scale, underpinned by deep clinical understanding, sector-leading quality ratings, and an unwavering focus on person-centred practice.


We keep our focus on maintaining high-quality standards across all our services, consistently achieving sector-leading regulatory ratings across the UK. 81% of services evaluated earned a Good or Outstanding rating by regulators, outperforming the national average. Cygnet has 17% higher CQC Good or Outstanding ratings than the rest of the mental health independent sector and 95% of our hospitals are rated Good or Outstanding by our internal quality assessment team. Our collaboration with 360 commissioning bodies, has not only allowed us to support integrated pathways of care, but has also helped shape local and regional strategies for individuals with complex needs.


Cygnet has also been recognised externally, with recent wins at the HealthInvestor Awards including Specialist Care Provider of the Year and has also been recognised by the Carers Trust, with 20 of our services being awarded Triangle of Care accreditation.


Reporting directly to the Group Clinical Director, this is a full-time position responsible for strategic leadership of our Health Care South region (Including Greater London, South East, South West, South Wales and West Midlands). This is a remote role but will include travel to sites within this region 2 – 3 days per week, so access to a car & UK driving licence is essential.



Key Responsibilities:


Strategic and Clinical Leadership


  • Provide strategic clinical leadership across the division, setting high standards for medical practice and professional conduct.
  • Ensure alignment with national clinical policy and statutory requirements, championing evidence-based care, prevention, early intervention, and integrated models of service delivery.
  • Promote a strong culture of patient safety, learning, and openness in line with Just Culture principles.


Clinical Governance and Quality Improvement


  • Oversee clinical governance frameworks to ensure safe, effective, and person-centered care.
  • Lead on clinical quality improvement, audit, and innovation initiatives, ensuring high standards of care are maintained and continuously enhanced.
  • Promote adherence to policies relating to safeguarding, medicines optimisation, infection prevention and control, and controlled drug safety.


Medical Workforce Leadership


  • Lead on all aspects of clinical workforce planning, including recruitment, retention, role redesign, and succession planning.
  • Ensure a high-performing and appropriately skilled clinical workforce through oversight of appraisal, revalidation, CPD, and professional development.
  • Embed a culture of reflective practice, supervision, and 360-degree feedback within medical leadership.


Operational Excellence and Resource Stewardship


  • Work closely with the respective Managing Directors and regional clinical directors to ensure high-quality and high-value service delivery.
  • Ensure clinical productivity and resource utilisation are optimised, with clear outcome measures and benchmarking in place.
  • Contribute to the achievement of the overall financial targets by the division.


Innovation, Research and Partnership


  • Foster academic and clinical partnerships with external stakeholders, including NHS bodies, academic institutions, and research networks.
  • Promote engagement in ethically approved research, supporting a culture of inquiry, learning, and evidence-based practice.
  • Champion patient and resident involvement in research to inform service development and improve care outcomes.


We are looking for someone who is…


  • Extensively experienced in senior medical leadership, ideally at Associate Medical Director, Regional Medical Director, Divisional Director or equivalent level.
  • Holds an in-depth understanding of clinical and corporate governance frameworks.
  • Has comprehensive knowledge of the professional, educational, and regulatory requirements of the medical workforce.
  • Experienced in service redesign, workforce transformation and strategic planning.
  • Demonstrates a proven ability to lead change, manage complex teams and influence across organisational boundaries.
  • Demonstrates commitment to quality improvement and evidence-based practice in a multi-disciplinary setting.
  • Holds strong financial and budget management skills (desirable).
  • Experienced in medical research, audit, and clinical effectiveness.
  • Shows high emotional intelligence and excellent interpersonal skills, with the ability to navigate complexity and foster consensus.
  • Excellent written, verbal, and presentation skills, with the ability to engage diverse stakeholders.
  • Committed to ongoing personal and professional development, including the use of feedback tools such as MSF/360 appraisal.
  • Fully registered GMC & MBBS (or equivalent) qualified, and registered on the specialist register (CCT/CESR), Section 12 and AC Status


Why Cygnet? We’ll offer you…


  • Market leading salary and bonus
  • Company shares
  • Travel allowance
  • Generous annual leave entitlement that increases with length of service
  • Company paid Life Assurance scheme covering 3x salary
  • Contributory pension scheme
  • Electric Car Scheme
  • Free meals, on-site parking and EAP support
  • Research and teaching opportunities, as well as the opportunity to lead and participate in QI & Audit initiatives
  • A unique opportunity to lead the development of new services within the independent sector, shaping an innovative model of care from the ground up
  • Extensive development opportunities and monthly CPD groups
  • Peer‑led “Characters of Care” programme and a comprehensive employee benefit and support programme
  • Company Funded Cash plan with the ability to claim up to £1000 per annum worth of benefits including free Physiotherapy, Osteopaths, Optical, dental, consultations, scans and free prescriptions
  • Gym Discounts across the UK as well as free online fitness classes with ClassPass, Nutritional Programmes and Fitness Consultations
  • Discount schemes including Reward Gateway, NHS Discount and Blue Lights Card
  • Smart Health Toolkit, including 24 hour GP service with the option of prescription delivery to your local pharmacy


If you would like to discuss this informally we’d be more than happy to facilitate this. Please contact: Hannah Dunlop via or 077 20 497 792


Requirements


The successful candidate will be required to undergo an enhanced DBS and reference check and an offer of employment will be subject to successful clearance.


*Recruitment agencies please note: Speculative emails are not to be sent directly to our clinical staff, these need to go via our internal recruitment team. If speculative candidates are sent directly to a member of the clinical team, we will consider these candidates as our own*

This advertiser has chosen not to accept applicants from your region.

Medical Director - Ophthalmology

Rochdale, North West Practice Plus Group

Posted 14 days ago

Job Viewed

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Job Description

About The Role

Are you an experienced Consultant Ophthalmologist ready to take the next step in your career? This is a unique opportunity to combine your clinical expertise in ophthalmology with a strategic leadership role as our Medical Director at Practice Plus Group.

You’ll join a respected, innovative organisation delivering high-quality care to NHS and private patients. In this pivotal role, you’ll shape ophthalmology services, drive continuous improvement, and lead a dedicated team to deliver outstanding patient outcomes.

To apply for the role click on the link below. If you have any questions contact in our friendly resourcing team, or call 07753313395.

We will contact all shortlisted candidates but please note Practice Plus Group retain the right to remove the advert prior to the closing date if a suitable candidate is appointed. Our employment offers are subject to receipt of satisfactory pre-employment checks. At Practice Plus Group, we actively promote diversity and equal opportunities. Applicants must have the right to work in the UK.


What you'll be doing


As our Medical Director with an Ophthalmology background, you will:

· Provide visible, inspirational clinical leadership for our ophthalmology service and wider hospital team

· Oversee governance, compliance, and patient safety, ensuring care meets and exceeds CQC and national standards

· Maintain a regular clinical commitment in ophthalmology (sessions to be agreed), ensuring you remain close to patient care

· Lead service development and transformation projects, including expanding pathways and improving access to high-quality eye care

· Work in partnership with the Hospital Director and Head of Nursing to deliver operational and strategic objectives

· Contribute to national reporting and best practice initiatives (e.g., GIRFT, NOD)

· Support the recruitment, training, appraisal, and development of medical staff

· Act as the primary clinical representative with external stakeholders, commissioners, and professional bodies

· Drive innovation


As a GMC-registered Consultant Ophthalmologist on the Specialist Register, you will also have:

  • Significant post-registration experience with a track record of excellence in cataract and general ophthalmology surgery
  • Experience in clinical leadership or an interest in moving into a formal leadership role
  • Passion for delivering patient-focused care and continuous service improvement
  • Knowledge of national ophthalmology pathways and performance frameworks
  • Excellent communication, influencing, and teamworking skills
  • Ability to balance clinical, operational, and strategic priorities
  • Commitment to maintaining and developing your own clinical practice alongside leadership responsibilities
  • MBA or postgraduate qualification in leadership, management, or healthcare quality – desirable
  • Experience in service transformation, pathway redesign, or private ophthalmology provision – desirable
  • Familiarity with GIRFT, NOD, and NHS national reporting programmes – desirable


What you can expect in return;


  • Competitive rate of pay
  • An extensive range of wellbeing and lifestyle benefits
  • 25 days holiday per year plus Bank Holidays
  • Private Pension with employer and employee contributions
  • 10 CPD days per year
  • Flexible shifts that enable you to work around other commitments
  • The support you need to grow in your role and continue your professional development
This advertiser has chosen not to accept applicants from your region.

Medical Director Clinical Development

Greater London, London ARTO

Posted today

Job Viewed

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Job Description

ARTO is currently partnered with a globally renowned mid sized Pharmaceutical company who are committed to the development of drugs within the Rare Disease space.


With a growing clinical development team, we are currently searching for a Medical Director in their Clinical Development group who will be able to assist with the development of drugs from proof of concept up to the crucial NDA/BLA submission phase.


Key Responsibilities:

  • Medical Oversight : Acts as Medical Monitor, overseeing study execution, subject eligibility, and safety surveillance.
  • Scientific Leadership : Provides medical input on clinical study and protocol design, as well as driving clincial and project groups through execution
  • Data Analysis & Interpretation : Critically evaluates study data and contributes to the integration and interpretation of results.
  • Strategic Contribution : Supports the Clinical Development Plan (CDP) by aligning studies with broader clinical and scientific strategy.
  • Stakeholder Collaboration : Engages with internal teams and external physician stakeholders to inform clinical decisions and ensure relevance.


Experience Needed:

  • MD/MD PhD
  • 5 Years experience in the pharmaceutical industry
  • Experience as a Clinical Lead
  • Rare Disease experience preffered, but experience developing drugs in the wider Immunology space is also acceptable


If you'd like to hear more, please reach out to me on , or directly on LinkedIn DM!

This advertiser has chosen not to accept applicants from your region.
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Medical Director Clinical Development

Cambridge, Eastern ARTO

Posted today

Job Viewed

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Job Description

ARTO have partnered with a highly funded biotechnology company with an innovative preclinical platform looking to find therapeutic candidates for diseases in Autoimmune, Neurological and Cardiovascular diseases.


As their research moves towards the clinic and phase I, we are now searching for a Medical Director to oversee the drafting of the IND packages, prepare for the company's drug development plan and also be a key member of the R&D team.


For this position, the ideal candidate would be based in the UK, with a bi-weekly office expectation of roughly 3 days in Cambridge.


Responsibilities:

  • Implement translational medicine and early clinical development plans for different therapeutic candidates
  • Prepare for Phase I clinical trials
  • Design and Implement clinical development plans
  • Lead the prep of regulatory submission documents.
  • Build relationships with stakeholders, senior management, KOLs


Qualifications:

  • MD, with experience working as a Clinical lead for early phase clinical trials.
  • Strong scientific background in Immunology/Inflammation/Dermatology and exposure and understanding of multiple disease areas and also drug development/discovery processes
  • Proven experience leading Phase I and II clinical trials.
  • At least 5 years of experience in industry from a pharmaceutical/biotech company.
  • Ability to work hands on in a dynamic team.


+447476557042

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TA Medical Director - CRM

London, London Novartis

Posted today

Job Viewed

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Job Description

full time
Summary
The UK Medical Director for Cardiovascular, Renal and Metabolic disease is responsible for driving integrated medical affairs plans for pipeline, launch and marketed products and developing and leading the medical TA team.
About the Role

Location:
London Office with Hybrid working (12 days per month in the office)

#LI Hybrid

Major accountabilities:

Manage and develop the performance and development of the CRM TA Medical team
Effectively incorporate lead metrics to ensure impact of our medicines for patients
Demonstrates enterprise leadership and the medical strategy as key member of the UK Medical Leadership Team.
Drive best-in-class launch preparedness & launch execution
Builds bold external partnerships beyond traditional Healthcare professionals
Represent Novartis at key external governmental, scientific, clinical and medical events
Encourages utility of more digital technologies for more data generation & utilization, in collaboration with the HCS
Ensures country evidence gaps are based on solid customer feedback

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Requirements

Advanced degree in life sciences MD, PharmD, or PhD (Preferred)
Significant work experience in Medical Affairs in the Pharma/Biotech/Healthcare industry
Experience of directly managing a team of people, with evidence of creating great work cultures, developing people and acting as an authentic and inspiring leader
Deep understanding of the UK healthcare system
Launch and pipeline management experience is key
Deep understanding of drug development and approval processes, including experience designing and/or executing of clinical studies
Highly collaborative with the ability to work in a matrixed business environment
Business mindset with the courage to challenge the status quo
CRM TA specific experience is desirable

You’ll receive:

Competitive salary, Annual bonus, Pension scheme, Share scheme, Health insurance, 25 days annual leave, Flexible working arrangements, subsidized dining facilities, Employee recognition scheme, learning and development opportunities.

Why consider Novartis?

766 million. That’s how many lives our products touched in 2021. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?

We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.

Imagine what you could do at Novartis!

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: />
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? />
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: />
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: />Division
International
Business Unit
Universal Hierarchy Node
Location
United Kingdom
Site
London (The Westworks)
Company / Legal Entity
GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
This advertiser has chosen not to accept applicants from your region.

(Associate) Medical Director - Neurology

ThermoFisher Scientific

Posted 13 days ago

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Job Description

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
**A day in the Life:**
+ Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
+ Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
+ During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions' dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
+ Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
+ Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
+ Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
**Education**
+ MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Neurology patients in hospital practice.
**Knowledge, Skills, Abilities**
+ Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
+ Is fluent in spoken and written English
+ Shown understanding and experience with NDA submission process.
+ Shown understanding of regulatory guidelines for adverse event reporting
+ Strong communication & presentation skills and is a strong teammate
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
 

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