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📍Location: Maidenhead, England, UK | 🔄Self-Employed | ⏰ Flexibility to manage your own calendar | 🤝In-Person Counselling services | 💼Own professional consulting premises Are you a qualified mental health professional looking to make a meaningful impact while enjoying flexible working arrangements? 🚀 Why Choose TELUS Health? • Comprehensive Support - Thorough induction training with dedicated Team Managers, • Professional Growth - Diverse case exposure and enhanced short-term counselling expertise, • Flexibility - Full control over referral acceptance and scheduling, • Technology- Access to our intuitive Provider Hub platform, • Community - Strong peer relationships and ongoing management support, • Development - Regular audit feedback and free CPD Learning Line events, • Insights - Customer satisfaction data to inform your practice 🎯 What You'll Do: • Manage online referrals with prompt response times, • Provide short-term, solution-focused counselling (3-12 sessions), • Connect with diverse clients facing varied workplace and personal challenges, • Maintain comprehensive case documentation and feedback, • Collaborate with our Provider Services team on risk management 📋Essential Requirements: • Accreditation: BACP/UKCP/COSCA/BPS/NCS/BABCP or equivalent, • Alternative: Diploma-level qualification + 3 years post-qualification experience + 450+ counselling hours, • Approach: Experience in short-term, solution-focused therapeutic models, • Supervision: Regular professional clinical supervision arrangements should be in place, • Insurance: Professional indemnity (minimum £1,000,000), • Compliance: ICO registration as Data Controller 🎓 Ideal Experience: • Previous EAP experience preferred but not essential, • Assessment and support planning expertise, • Short-term counselling interventions with workplace focus, • Understanding of organizational dynamics and work-life challenges, • Knowledge of local therapeutic resources and referral pathways, • IT proficiency (Microsoft Office, email, online systems)

Senior Regulatory Affairs Manager CMC – Europe Slough – Hybrid. Full time, Permanent This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. The role involves strategic input into development programs, preparation and submission of regulatory documentation, and post-approval lifecycle management and due diligence reviews. You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities. Key Responsibilities: • Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions., • Review non-clinical and clinical data packages for regulatory adequacy and compliance., • Conduct due diligence across CTD Modules 1–5 and review sections of Marketing Authorisation Applications (MAAs)., • Coordinate registration and maintenance of assigned generic products., • Support regulatory authority interactions, including scientific advice procedures., • Maintain regulatory databases and document management systems., • Guide junior staff and contribute to process improvements within the regulatory function., • Ensure alignment with EU regulatory requirements for product launch and lifecycle activities. Required Experience & Qualifications: • Strong, clear evidenced experience with European regulatory frameworks and submission pathways (DCP, MRP, national procedures)., • Proven experience in regulatory strategy development for specialty and generic products- minimum 7 years industry experience, • Hands-on experience with post-approval activities, variation strategies, line extensions and due diligence activities is essential., • Familiarity with regulatory tools and platforms (eCTD, CESP, MHRA portal, Eudralink)., • Ability to critically evaluate scientific data and identify regulatory risks and mitigation strategies., • Degree or higher qualification in Pharmacy, Life Sciences, or a related field., • Excellent communication, project management, and cross-functional collaboration skills., • Experience managing regulatory timelines and approvals in a fast-paced environment.

📍Location: Marlow, England, UK | 🔄Self-Employed | ⏰ Flexibility to manage your own calendar | 🤝In-Person Counselling services | 💼Own professional consulting premises Are you a qualified mental health professional looking to make a meaningful impact while enjoying flexible working arrangements? 🚀 Why Choose TELUS Health? • Comprehensive Support - Thorough induction training with dedicated Team Managers, • Professional Growth - Diverse case exposure and enhanced short-term counselling expertise, • Flexibility - Full control over referral acceptance and scheduling, • Technology- Access to our intuitive Provider Hub platform, • Community - Strong peer relationships and ongoing management support, • Development - Regular audit feedback and free CPD Learning Line events, • Insights - Customer satisfaction data to inform your practice 🎯 What You'll Do: • Manage online referrals with prompt response times, • Provide short-term, solution-focused counselling (3-12 sessions), • Connect with diverse clients facing varied workplace and personal challenges, • Maintain comprehensive case documentation and feedback, • Collaborate with our Provider Services team on risk management 📋Essential Requirements: • Accreditation: BACP/UKCP/COSCA/BPS/NCS/BABCP or equivalent, • Alternative: Diploma-level qualification + 3 years post-qualification experience + 450+ counselling hours, • Approach: Experience in short-term, solution-focused therapeutic models, • Supervision: Regular professional clinical supervision arrangements should be in place, • Insurance: Professional indemnity (minimum £1,000,000), • Compliance: ICO registration as Data Controller 🎓 Ideal Experience: • Previous EAP experience preferred but not essential, • Assessment and support planning expertise, • Short-term counselling interventions with workplace focus, • Understanding of organizational dynamics and work-life challenges, • Knowledge of local therapeutic resources and referral pathways, • IT proficiency (Microsoft Office, email, online systems)

The successful candidate will conduct and present detailed analyses of clinical and health data and collaborate closely with Statisticians.

A health service provider in the North East UK seeks a Senior Administrator / Clinical Coder to ensure accurate clinical data entry and promote effective use of health information.

A leading clinical research organization is seeking a Senior Data Scientist to lead advanced analyses and develop predictive models to inform clinical study designs. This role contributes to team growth and supports data-driven decisions, impacting patient outcomes in the pharmaceutical sector.

A leading healthcare company in the UK is seeking a Lead Data Scientist to design and develop LLM-based solutions that accelerate drug development and improve patient care.

A leading NHS foundation trust is seeking a Clinical Coder to provide high-quality coded clinical data. This role involves extracting and coding complex clinical information to meet reporting and governance deadlines.

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. The Associate Clinical Data Manager will be the escalation point and poi

A leading research institution in Greater London seeks an experienced Clinical Trial Manager to oversee the trial management of an innovative project aimed at tackling antimicrobial resistance.

A leading NHS Trust in Greater London is seeking a Clinical Informatics Specialist to enhance clinical practices through data analysis and user-friendly tools. This role involves supporting the Clinical Informatics Service via project implementation and sustainability efforts. Ideal candidates shoul

A leading health technology company in Witney is seeking a Principal Clinical Data Management Analyst to provide team leadership and clinical data management expertise for Clinical Affairs and R&D. The role involves managing data management activities across clinical studies and R&D projects and dev

A leading biopharmaceutical company is seeking a Senior Manager, Data Management to lead clinical studies and oversee data management activities. Ideal candidates will have over 6 years of experience in clinical data management, strong project management skills, and the ability to lead team initiati

A leading biostatistics firm is seeking an experienced professional to provide technical leadership in SAS programs for analyzing clinical trial data.

Strong knowledge of clinical data management processes and regulatory requirements (GCP). This role serves as the primary point of contact for data management on assigned projects, ensuring high-quality deliverables are completed on time, within budget, and to client satisfaction. Lead and manage da

A global pharmaceutical company seeks a Lead Data Scientist in Clinical AI to develop LLM-based and ML solutions for drug development.

A clinical research company in the UK is looking for a Data Analyst I to provide backend support for the Financial Team. This role involves processing data and reconciling payments for clinical research studies.

A leading global healthcare consulting firm is seeking a Senior Data Manager to oversee data management for clinical trials.

Support the delivery of clinical research in accordance with Good Clinical Practice (GCP), the Declaration of Helsinki, applicable legislation (including, but not limited to, the Medicines for Human Use Clinical Trials Regulations, Data Protection Act 2018, Human Tissue Act), the Research Governance

This senior-level position focuses on advanced analyses of clinical trial data, developing predictive models, and creating compelling data visualizations. A leading clinical research organization in Greater London is seeking an experienced informaticist to join the Informatics team.

A leading NHS foundation trust in Greater London seeks a Clinical Coder responsible for providing high-quality coded clinical data. The role involves analyzing and coding complex clinical information, requiring an academic background and clinical coding experience.

Acts as Functional Lead for Data Management including primary contact for internal liaison between Data Management/Operations and Project Management, Clinical Monitoring, and other functional groups. Medical Writing Developer (Data Management - Clinical Programming). Coordinate the work of the assig

A healthcare organization in the North East of England seeks a Systems Support Analyst to implement and maintain clinical applications and provide technical support.

A clinical contract research organization is looking for a Clinical Application Administrator to join their IT department in Greater London. Responsibilities include troubleshooting, user training, and data import between systems.

Data Management plan (DMP), Data Validation Plan (DVP), Data Entry Guideline, Database Specification Document (DBSD), Database Report (DBR)) in the DM TMF. Export data from the clinical database to authorized recipients (e. Perform clinical database development, including data entry screen design, t

A clinical research organization is seeking a Clinical Data Manager to lead data processing and management activities for clinical trials. This role requires a Bachelor's degree and at least 2 years of experience in clinical trial data management. You will be responsible for managing timelines, ensu

Data Analytics, Microsoft Access, SQL, Power BI, R, Data Visualization, Tableau, Data Management, Data Mining, SAS, Data Analysis Skills, Analytics. Support clinical studies including CRF design/review database build and validation creation of data management documents. Principal Clinical Data Manag

The role involves managing clinical research data, ensuring accuracy, and providing support to multi-disciplinary research groups. A leading global university in the UK seeks a Senior Data Manager for the Birmingham Clinical Trials Unit. Candidates should have a degree in a biomedical field and expe

This is an exciting opportunity to undertake a one-year clinical fellowship, designed to provide sub-specialty experience in pulmonary intervention.

A leading global healthcare consulting firm in the United Kingdom is seeking an experienced Senior Data Management Programmer. The role involves leading programming tasks for clinical trials while owning specifications and validation processes. Candidates should have 5+ years of SAS programming expe

The role involves coding medical information, supporting clinical staff, and ensuring accurate data entry into the organization's systems.

A full-service clinical contract research organization in Greater London is seeking an experienced informaticist to lead advanced analyses and create predictive data models.

A leading biopharma company is seeking a Clinical Trials Specialist Apprentice to support the planning and delivery of clinical trials. The role involves assisting with setup, data management, documentation, and site coordination.

The post holder will be required to accurately enter large amounts of research and patient data and to ensure that the data are stored appropriately according to the data protection act and in line with the ethical approval for the projects involved. Accurately and efficiently enter patient data on

A healthcare organization in Greater London is seeking a dedicated Clinical Trial Assistant to provide administrative and data management support to their research team. The ideal candidate will have experience with clinical trials and strong communication skills.

A leading medical laboratory hub in the UK is seeking a candidate for a role focused on medical coding and administration of clinical data. The responsibilities include ensuring data security, summarizing medical information, managing risk in practices, and mentoring junior staff.

The ideal candidate will possess senior-level experience in clinical trials, a strong background in research methodology, and the ability to audit clinical data while ensuring regulatory compliance. A leading AI technology firm is seeking a Principal Clinical Scientist to drive expertise in clinical

A leading global biopharmaceutical solutions organization is seeking a Sr Clinical Data Scientist to lead the coordination of data collection for clinical studies. Candidates should have experience with Veeva Vault and a strong background in clinical data management. This role involves ensuring data

Proclinical is seeking a Clinical Data Manager to join a dynamic team focused on improving patient outcomes in cardiothoracic surgery. In this role, you will play a key part in enhancing database onboarding, data curation, and ensuring data quality. Ready to shape the future of cardio‑thoracic res

A prominent pharmaceutical company in Hertfordshire is looking for a Clinical Database Programmer to support the transition to electronic data capture. The role involves building and maintaining study databases, ensuring data quality, and managing data integration with external vendors. Candidates s

Key performance indicators dictated by Healthcare for London and patient outcomes are monitored and assessed regularly, and an active programme of internal audit within the stroke service provides essential data for clinical governance purposes. Standard Operating Procedures (SOPs) for major element

A leading health tech company in the UK is seeking a Senior UX Designer to shape data-driven, AI-enabled experiences in clinical trials.

Key responsibilities include ensuring high standards of data collection, managing trial documentation, and supporting the clinical research team. This role does not involve patient contact and is crucial for the efficient delivery of clinical trials as well as compliance with GCP standards. A leadin

A leading healthcare provider in Greater London seeks an Administrative and Data Management Assistant to support their research team. Responsibilities include managing office operations, assisting in clinical trial recruitments, and coordinating specimen storage. Ideal candidates should be proficien

A leading clinical research organization in the United Kingdom is seeking a Data Manager to oversee and coordinate data management activities in clinical projects. Successful candidates will have experience in data management, strong communication skills, and an understanding of clinical trial proce

A leading life science consulting firm in the United Kingdom is looking for a Data Manager to oversee the data management strategy for various projects. The ideal candidate will have a Bachelor's degree in Mathematics and experience in clinical trials. Responsibilities include developing metrics rep

Acts as central steward of clinical data quality, monitors risks through the holistic review of clinical and operational data, using high level knowledge of the protocol, taking into account the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross f

To provide sound clinical leadership and develop support mechanisms for sharing good practice within the clinical setting and Trust wide. Maintain and update own clinical expertise and contribute as role model to ensure the delivery of nursing care is at highest possible level to meet patient care.