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Job Description Senior MSK Outpatient/Orthopaedic Inpatient Physiotherapist Full time 37.5Hours Ashtead Hospital The role: We are looking for a highly motivated individual with proven skills in the management of musculoskeletal physiotherapy and orthopaedic inpatients to work 37.5 hours per week, hours can be flexible but will ideally cover one later shift. The role will consist of at least 3 days outpatient caseload and inpatient hours as the service requires. Requirements: • Working as part of the Physiotherapy Team to provide a high standard of efficient, individualised, evidence based patient care., • A strong communicator with exceptional standards for customer service standards. Adhering to all of Ramsay’s policies and procedures to ensure the best possible clinical outcomes for patients. A strong advocate of the Ramsay Way and People Caring for People., • Delivering high quality physiotherapy care in a hospital setting; including the assessment, treatment, planning and development of physiotherapy treatment programmes, progressing treatment using own clinical knowledge and justification, • High regard and implementation of health and safety and infection control procedures regarding patients, colleagues and the environment at all times, • A commitment to CPD, mandatory training and e-learning, evidence based practice and personal development, • A good standard of IT literacy and willingness to learn new information technology as required, • Working effectively and independently as part of the Physiotherapy team and the wider multi-disciplinary team., • Have evidence of further professional training and continual professional development, reflecting your desire to develop as a practitioner Essential: • BSc Honours degree in Physiotherapy/equivalent, • HCPC and CSP registered, • Experience of working as an outpatient and inpatient orthopaedic Physiotherapist with at least 3 years experience., • Evidence of CPD, • Have a sound understanding of the CSP standards of practice and HCPC standards and how they relate to individual practice. Benefits • 25 Days Leave + Bank Holidays, • Buy & Sell Flexi Leave Options, • Private Pension where Ramsay will match up to 5% after a qualifying period, • Flexible shift patterns available where possible, • Enhanced Competitive Parental Leave Policies, • Private Medical Cover with option to add partner & dependants, • Life Assurance (Death in Service) x3 base salary, • Free Training and Development via the Ramsay Academy, • Subsidised staff restaurant, • Concerts for Carers, • Employee Assistance Programme, • Cycle2Work scheme available, in partnership with Halfords, • The Blue Light Card Scheme About us We’re Ramsay Health Care UK. With 35 hospitals, 7,600 staff and 200,000 patients treated every year, we’re one of the leading independent healthcare providers in England. We deliver a wide and comprehensive range of specialised clinical services from routine to complex surgery, day case procedures, cancer care, diagnostic services and physiotherapy. In addition, we also have our three standalone decontamination units which are essential to supporting our clinical outcomes. 94% of our facilities are rated ‘Good’ by the CQC, and we are extremely proud of the high quality of our staff as well as excellent relationships with doctors and our strong, longstanding partnership with the NHS. We’re part of a global hospital group with over 50 years’ experience that operates in 11 countries across the world. As people caring for people, our ethos helps make a huge difference in the lives of millions. We know that our people are our most important asset to our organisation, and are the key to our success and continuing growth. To apply Please contact: Sally Mirtle (Physiotherapy Manager) for an informal chat or to ask any questions you may have before you apply. We are committed to equality of opportunity for all. This position is subject to an Enhanced DBS check. We reserve the right to close our adverts prior to the announced closing date to ensure a quality recruitment process. We care. It’s more than what we do, it’s who we are. Everything we do is about striving to deliver the best care. And it's a belief that's as true today as it was when we welcomed our first patients in 1964. “The Ramsay Way” culture recognises that our people are our most important asset and this has been key to our ongoing success. We are proud to support the UK’s Armed Forces and Reservists and have already achieved the Silver Award as part of the MOD’s Armed Forces Covenant Employer Recognition Scheme. The scheme recognises employers who actively support Defence while encouraging other organisations to adopt the same behaviours in their workplace. As a company we are committed to supporting the wider Armed Forces community and this includes our staff as well as our patients. We are committed to equality of opportunity for all. This position is subject to background and DBS checks. We care. It’s more than what we do, it’s who we are. Everything we do is about striving to deliver the best care. And it's a belief that's as true today as it was when we welcomed our first patients in 1964. “The Ramsay Way” culture recognises that our people are our most important asset and this has been key to our ongoing success. We are proud to support the UK’s Armed Forces and Reservists and have already achieved the Silver Award as part of the MOD’s Armed Forces Covenant Employer Recognition Scheme. The scheme recognises employers who actively support Defence while encouraging other organisations to adopt the same behaviours in their workplace. As a company we are committed to supporting the wider Armed Forces community and this includes our staff as well as our patients. We are committed to equality of opportunity for all. This position is subject to background and DBS checks.

We are seeking a Regulatory Affairs Manager to join our global team based in Hampshire, UK. The Regulatory Affairs Manager role offers you an exciting opportunity to join our highly motivated Product Development – Injectables team, a patient-centric, fast paced environment focused on rare diseases. This position operates within Alimera Sciences Limited, a subsidiary of ANI Pharmaceuticals, with a 3 day per week in office expectation. If you are a regulatory professional with European experience who is looking to expand and grow in their career, then this could be an excellent opportunity for your development! It is a global role, with a primary focus on our international (non-US) markets, which will provide opportunity for you to expand your international and US regulatory experience across a wide breadth of projects and submissions. The successful candidate will be responsible for leading regulatory activities for international projects, providing regulatory guidance and liaising with external partners including regulatory authorities. This role is a key member of a highly visible team and provides prominent exposure across multiple business units and with leadership. As a dynamic growing company, this role values accountability, adaptability and a proactive mindset to support the company’s expansion. TASKS / RESPONSIBILITIES • End to end management of complex global projects and submissions, from developing strategies through to the filing of applications and post-approval implementation., • Oversee and support licensing partners in international regions (including Middle East, Asia, Australia)., • Responsible for a range of submissions from initial authorisation applications, variations/supplements, annual reports through to clinical trials and educational materials., • Regulatory point of contact for key projects, collaborating closely with multiple cross-functional areas including PV, Quality, Manufacturing, Supply, Medical and Marketing., • Understand, interpret and advise on regulatory legislation and guidance., • Interact with regulatory authorities to facilitate successful submissions and approvals., • Author high quality Common Technical Dossier (CTD) modules and regulatory technical documents., • Input into cross-functional submission documents, e.g. clinical protocols, PSUR, DSUR, PADER, educational materials, quality/manufacturing reports., • Management of regulatory labelling texts, including coordination of translations. PROFESSIONAL QUALIFICATIONS/EXPERIENCE • Degree in life sciences, engineering, pharmacy or higher, • Minimum of 5 years experience in European Medicinal Regulatory Affairs., • Proven ability to accurately assess regulatory impact, develop effective strategies and deliver submissions. Prior experience with European MRP/DCP is required., • Excellent written and verbal communication skills in English., • Experienced at authoring regulatory technical and submission documents., • Proven track record with navigating post-approval CMC changes, including ability to identify regulatory impact, data requirements and achieve successful filings., • Sound performer in interacting with and influencing regulatory authorities., • Prior US medicinal regulatory affairs experience and familiarity with global regulations, including US, is beneficial but not required. Knowledge of medical devices and drug-led combination products is desirable. SKILLS AND COMPETENCIES • Effective and influential communicator – you have strong verbal and written skills, able to clearly convey regulatory positions and persuade internal and external stakeholders., • Broad knowledge of European regulatory systems, including relevant current and upcoming legislation, • You can understand and interpret regulatory legislation and guidance documents., • Self-motivated, self-reliant and able to work independently in a fast-paced, deadline driven environment., • Effective networker and team worker – you are able to build effective working relationships with colleagues, external partners and regulatory authorities., • Strong analytical thinking and problem-solving skills, with a high attention to detail. Proven ability to deliver well thought-through and evaluated solutions., • Sound project management and organizational skills – you are able to effectively plan time and prioritize to achieve goals., • Flexible approach – able and eager to learn new things, think creatively and laterally, and think outside the box. Willingness to roll up your sleeves and get things done.

HUB LABELING MANAGER Location: Walton Oaks Contract Type: 12‑month Temporary Contract Salary: £40,000–£45,000 per annum JOB SUMMARY Summarize the primary purpose & key accountabilities of the job. The Manager is responsible for preparation of LPDs, associated LLDs and PLDs for nationally registered products for their assigned markets, and for updating labelling documents on a timely basis according to internal SOPs and external regulatory requirements. This role may act as a Subject Matter Expert (SME) on local, regional and multi‑country regulatory labelling requirements and collaborate with other Hub Labelling Managers to share intelligence. Additionally, this role serves as an SME for the use and development of global tools, technologies and processes used to support label development, submission and approval — with a particular focus on digital solutions. JOB RESPONSIBILITIES Primary responsibilities critical to the job: • Monitors system data integrity and performs quality checks., • Maintains system management for labelling activities including GDMS and approved labelling tracking systems., • Produces labelling‑related documentation for submission to HAs such as tracked‑change versions, annotated labels, comparison tables, and annotated supporting documentation., • Performs QC checks on work produced by colleagues., • Identifies incremental improvements to labelling‑related processes and systems for exploration by senior labelling managers., • Meets defined productivity, quality, and compliance targets as set by management., • Utilizes regulatory labelling expertise to review, develop and deliver labelling documents for submission to Regulatory Authorities across markets/regions, requesting medical input as appropriate., • Supports other deliverables within ILG responsibilities (e.g., readability testing)., • Contributes to projects involving current and new global tools, technologies, and processes supporting label development, submission, and approval — with a focus on digital solutions., • Participates in research incubator initiatives involving automation, machine learning, BPM, etc., • Collaborates with R&D leads on digital transformation initiatives aimed at integrating regulatory data, systems, and processes into a hyper‑efficient learning platform aligned to the GRS roadmap., • Assists with labelling data analysis., • Creates or enhances SharePoint web pages., • Produces the full range of labelling documentation including NCE labels, product extensions, and complex revisions., • Prepares responses to inquiries from colleagues during inspections and regulatory agency questions and represents during HA inspections. QUALIFICATIONS / SKILLS Skills (Associate Level) • Proficient in systems use consistent with business expectations; understands importance for maintaining compliance., • Fluent in English (additional languages advantageous)., • Strong written and verbal communication skills., • Understanding of SOPs, systems, and processes underpinning compliance and quality., • Experience working with structured data (enterprise databases, Excel, SharePoint, Access)., • Strong understanding of labelling principles and regulatory frameworks., • Ability to develop positive relationships across cultures and locations., • Strong attention to detail and problem‑solving skills., • Demonstrated technical aptitude and ability to learn new software quickly., • Ability to quickly learn regulations and standards., • Hands‑on registration experience in development, maintenance, or commercialization within Regulatory Affairs — ideally from a country office or regional regulatory perspective, especially understanding the implications of a CDS on LPDs., • Ability to understand and manage regulatory implications of product strategy relating to labelling., • Knowledge of global/regional regulatory guidelines, requirements, and clinical variations., • Ability to interpret and apply regional/local regulatory guidance (pre‑approval and post‑approval stages)., • Strong analytical, logical reasoning, and writing skills. ORGANIZATIONAL RELATIONSHIPS • Reports to Regional Labelling Head and International Labelling Team Lead., • Partners with PCOs, GRS, GRO and other platform lines as required., • Supports global, GRS, GRO, and ILG initiatives as needed. RESOURCES MANAGED May manage personnel within a matrix structure and may have direct line management responsibility for 1–2 individuals.

As a Clinical Services Manager at our luxury new care and nursing home in Surbiton, you'll play a key leadership role in ensuring exceptional person-centred care for our residents, supporting them to live safe, fulfilled lives.

As a Clinical Services Manager at our luxury new care and nursing home in Surbiton, you'll play a key leadership role in ensuring exceptional person-centred care for our residents, supporting them to live safe, fulfilled lives.

This is a great opportunity for a passionate and hands on nurse to join the home as a Clinical Deputy Manager.

We are looking for a Service Manager to lead our service at HMP Highdown in Sutton, Surrey, a Category C mens training and resettlement prison with a diverse and complex population. The Forward Trust delivers clinical and psychosocial substance misuse services across Surrey prisons, working in close

A respected independent optical practice in Leatherhead is seeking a Dispensing Optician Manager to lead their team.

A leading private healthcare provider in Sutton is seeking a Quality & Governance Manager to oversee clinical excellence and patient safety initiatives.

A leading private healthcare provider in Sutton is seeking a Quality & Governance Manager to oversee clinical excellence and patient Rang safety initiatives. Promote an excellent patient experience through quality initiatives.

We are looking for experienced Staff Nurses with an interest in developing their skills in the area of adult rehabilitation. To act for the Ward Manager/Senior Staff Nurse in their absence on an occasional basis ensuring that their operational and clinical standards and requirements are maintained.

As a Medical Case Manager, you will play a pivotal role in addressing the healthcare needs of our diverse patient base worldwide. Conducting routine medical case management activities with a focus on patient well-being and satisfaction. Prior experience in clinical case management is advantageous.

We are recruiting an experienced nurse to join our Government team as a Medical Case Manager. Conduct routine medical case management activities focused on patient well‑being and satisfaction. Prior experience in clinical case management is advantageous.

As a Multi‑Site Customer Experience Manager, you’ll create a culture and environment where customer‑facing teams deliver exceptional service and referrals across service lines to hospitals, clinical services, and other wellbeing centres as part of a holistic health‑care journey. Multi Site C

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world. Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. Promotes t

The Scientist for Clinical Trials - Oncology - Thoracic (Sr. Manager) ( non-MD ) is responsible for providing support of scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.

A leading biopharmaceutical company in the UK seeks a Scientist for Clinical Trials - Oncology (Senior Manager). The role involves ensuring the integrity and quality of clinical trials, mentoring team members, and collaborating with other departments. Candidates should have strong scientific backgro

Sessional Optometrist – Make a difference!. To undertake other duties commensurate with the role of optometrist under the instruction of the Special Schools Service Manager and Clinical Lead.

This role requires significant experience in clinical research and a strong background in oncology to ensure the integrity and quality of clinical trials. A leading pharmaceutical company in the UK is seeking a Senior Manager for Clinical Trials in Oncology.

DHC Talking Therapies is recruitingfor a Locality Manager to join our successful Talking Therapies team. To be responsible for the operational management of service delivery in a given locality, reporting to the Service Manager and working alongside the Clinical Team Leads, Lead Operations Administr

The team at Priors House Care Home have a great opportunity for a passionate and hands on nurse to join the home as clinical xwzovoh deputy manager.

Associate Product / Clinical Marketing Manager (Oncology Diagnostics). Associate Product / Clinical Marketing Manager. Actively contribute to new product development projects by providing market, clinical, and customer insights throughout the development lifecycle.

The Clinical Services Manager is a pivotal member of the Centre Leadership Team, shaping the culture, quality, and clinical standards of the Richmond centre; before, during and after opening. Are you a credible clinical leader who thrives in fast-paced environments, sets exceptional standards, and e

CLINICAL MANAGER JOB (MENTAL HEALTH). A CLINICAL MANAGER (MENTAL HEALTH). The Clinical Manager / Supervisor will be responsible for managing Patient Care Administration within assigned Service Area / Department in accordance with our accreditation and other regulatory bodies, recommending, developin

We are seeking a motivated Clinical Project Manager to drive site engagement across our clinical programs in Europe. As a Clinical Project Manager (CPM) in a site engagement capacity, you will serve as the key liaison between our clinical operations and investigative sites. Clinical Project Manager

Working closely with the Project Manager and Science Lead, the Associate Clinical Data Manager will be responsible for data cleaning and transfer of clinical neuroimaging data on a varied portfolio of neurology clinical trials. With our focus on neuroscience, our purpose is to advance human health b

Clinical Quality Assurance Manager (GCP). This role offers the opportunity to influence quality strategy, shape inspection preparedness, and drive continuous improvement across a growing clinical portfolio. QA support to clinical study teams.

Clinical Trial Manager – UK | Advanced Clinical (FSP Model). Advanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. Advanced Clinical offers a collaborative environment where your contributions directly support the success of

Offers clinical expertise and leadership as requested by their Clinical Director. CLINICAL MANAGER JOB (MENTAL HEALTH). A CLINICAL MANAGER (MENTAL HEALTH).

Were looking for an experienced Registered Nurse (RGN/RMN) to join our growing clinical team as a Clinical Case Manager for our Hull location. Youll provide expert clinical leadership, training, and support to our dedicated care teams. Wed love to hear from you if you have a current NMC registration

Associate Product / Clinical Marketing Manager (Oncology Diagnostics). Associate Product / Clinical Marketing Manager. Working closely with the CEO, senior external consultants, and internal R&D, clinical, and regulatory colleagues, you will play a leading role in shaping product positioning and go-

Clinical Case Manager Chemotherapy Salary starting from £45,365 per annum + car or car allowance Are you an experienced chemotherapy nurse ready to take your career beyond the bedside while still making a profound difference to patients lives? Were looking for a Clinical Case Manager (Chemotherapy

Deputy General Manager (RN)- Care HomeLocation: Ludlow, Shropshire, SY8 1LSHours: 40 hours per week (2 days supernumerary/ 2 days on shift)Pay: £49,266 per yearThe Role:Support the General Manager and lead the home in their absenceOversee care standards through audits, clinical supervision, and com

Clinical Nurse ManagerWhen registering to this job board you will be redirected to the online application form. Position:Clinical Nurse ManagerCare home: Potters GreenLocation: Rotherham, S64 5UWContract type: Full time, 40 hours per week, Monday to FridayRate: £50,377.

Manager)(non-MD)is responsible forproviding support ofscientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. Job ResponsibilitiesClinical development professional maintaining current scientif

Role: Clinical Manager Salary: £49787 - £55k per annum Onsite: Onsite 5 days per week Location: South West Role:Act as a clinical mentor to internal nursing and care staff. Panoramic Associates are supporting a care home in the South West with a substantive Clinical Manager position.

Fixed Term Contract - 9- 12 monthsClinical Deputy ManagerAre you an organised, methodical nurse who is passionate about delivering positive change? At Care UK you can build a fast-moving nursing career whilst help our residents fulfil their lives. The team at Manor Lodge Care Home have a great oppor

Are you ready to make a real impact in the care sector? Our client are looking for a Clinical Deputy Manager at their beautiful Bexhill-On-Sea care home.

The team at Manor Lodge Care Home have a great opportunity for a passionate and hands on nurse to join the home as clinical deputy manager.

Our client is seeking an experienced and compassionate.This is an excellent opportunity for a Registered Nurse with a valid.

In this role, you’ll support the Service Manager in overseeing several key functions, including referrals, medical reports, document assessment, laboratory results and general clinical administration. Work closely with internal and external partners (GPs, clinical teams, hospitals, insurers).

Registered Care Home Manager - Nurse Required. An amazing opportunity has arisen for a Home Manager to join an established family‑run, Nursing & Residential Care provider, who provide a full range of care services for residents across 41 care homes in England and Wales. We are looking for an Quali

Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. Roles within the Clinical Trial Manage

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the United Kingdom, specifically in London and Stirling. Project Manager/Clinical Trial Manager experience at a CRO required

A luxury care provider in Bedford seeks a passionate and experienced Deputy Home Manager (Nurse Qualified) to lead a dedicated nursing team. This full-time role offers a competitive salary of £62,000, focusing on clinical guidance, staff development, and ensuring high-quality care delivery.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. What The Proposals Manager - Writing Does At Worldwide.

A leading contract research organization in the UK is seeking an experienced Clinical Trial Manager to oversee project operations and ensure compliance with regulations. Interested individuals should possess a Bachelor’s in a related field and significant experience in clinical trial management.

Freelance/Contract Regulatory Affairs Project manager - Clinical trial applications (CTA's) page is loaded## Freelance/Contract Regulatory Affairs Project manager - Clinical trial applications (CTA's)time type: Full timeposted on: Posted Yesterdayjob requisition id: JR 8656For the past 20 year