Clinical data jobs in St AlbansCrear alertas

📍Location: Harpenden, 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)

A leading healthcare company in Hemel Hempstead is seeking a Science and Marketing Communications Executive to transform clinical data into engaging content.

We are looking for a Science and Marketing Communications Executive who can bring clinical and scientific data to life—transforming technical knowledge into marketing content that resonates with our audience of healthcare professionals. Translate complex scientific data into clear, engaging market

An excellent opportunity has arisen for an experienced regulatory professional to join my client, an established Regulatory consultancy, on an initial 12 month contract basis - the contract can be on a 6 or 12 month basis, full time or part time and fully remote based! The ideal person will have full life cycle experience, from CTAs through to registrations. As well as offering exposure to a broad range of projects, you will also be responsible for producing regulatory training materials for use on the other side of the business which offers courses for aspiring regulatory professionals. Responsibilities will include: As a Regulatory Affairs Manager, you will play a crucial role in guiding our clients through complex regulatory landscapes and helping to educate industry professionals. This role is ideal for a versatile and enthusiastic individual with comprehensive EU and UK regulatory experience, particularly in CMC, who are eager to learn, tackle new challenges, and make a significant impact on our company's growth and success. Regulatory Strategy & Lifecycle Management Strategic Guidance: Develop and implement robust EU and UK regulatory strategies for pharmaceutical and biotechnology products, from early-stage clinical development through to marketing authorisation and post-approval maintenance. Full Lifecycle Support: Provide expert regulatory input for First-in-Human studies, clinical trial applications (CTAs/CTIS), Investigational Medicinal Product Dossiers (IMPDs), Investigational New Drug (IND) applications, Marketing Authorisation Applications (MAAs), and post-authorisation activities (variations, renewals). Regulatory Intelligence: Advise clients on evolving regulatory requirements, guidelines, and best practices in the EU and UK, identifying potential risks and opportunities. Agency Interactions: Prepare for and participate in scientific advice meetings and other formal interactions with regulatory authorities (e.g., MHRA, EMA). Regulatory Submissions: Authoring & Review Dossier Development: Lead or significantly contribute to the authoring, review, and compilation of high-quality regulatory dossiers and documents, ensuring compliance with relevant regulations and guidelines. Module 3 Expertise: Specialise in the preparation and review of Chemistry, Manufacturing, and Controls (CMC) sections (Module 3) for both clinical trial applications and marketing authorisation applications. Quality Assurance: Ensure all submissions are scientifically sound, well-structured, and presented in a clear, concise manner to facilitate efficient agency review. Response Management: Coordinate and draft responses to regulatory agency questions and deficiency letters, working collaboratively with client teams. CMC Regulatory Leadership Technical Translation: Translate complex manufacturing and quality data into clear, compliant regulatory submissions. Change Management: Provide regulatory oversight and support for manufacturing process changes, analytical method development, technology transfers, and site changes. Strategic Input: Offer strategic CMC input throughout product development to ensure regulatory compliance and optimise development timelines. Training & Professional Development Content Development: Collaborate with our training team to design, update, and enhance engaging training materials for our diverse range of regulatory affairs courses (e.g., Introduction to Regulatory Affairs, Excel, Expand programs). Delivery & Presentation: Deliver compelling presentations and lead interactive sessions for both our public courses and bespoke in-house client training programs. Mentorship: Potentially mentor junior professionals or course participants, sharing your expertise and fostering their growth in regulatory affairs. Thought Leadership: Contribute to our knowledge base through articles, webinars, or other content that highlights our expertise and thought leadership (optional, based on interest). Client Consulting & Relationship Management Trusted Advisor: Serve as a primary regulatory contact for assigned clients, building strong, long-term partnerships based on trust and expertise. Problem Solving: Provide pragmatic, solution-oriented regulatory advice that addresses client challenges while maintaining compliance. Project Management: Manage regulatory projects effectively, ensuring timely delivery of high-quality work within agreed-upon scopes. Internal Contribution & Company Growth Process Improvement: Actively contribute to the continuous improvement of our internal processes, templates, and best practices. Strategic Input: Provide valuable insights and feedback to help shape the development of new consulting services and training offerings. Team Collaboration: Work closely with a supportive and collaborative team, contributing to our vibrant company culture. TPBN1_UKTJ

Psychological Wellbeing Practitioner (PWP) - HMP The Mount Location: Hertfordshire Salary: £28,407 Vacancy Type: Permanent Advertising End Date: 13 th February 2026 We are seeking an enthusiastic and dedicated Psychological Wellbeing Practitioner (PWP) to join our team supporting adults experiencing common mental health difficulties such as anxiety and depression. As a PWP, you will play a key role in assessing service users' suitability for evidence-based psychological interventions and delivering Step 2 low-intensity therapies in line with the Improving Access to Psychological Therapies (IAPT) framework. Interventions may be delivered individually, face-to-face, or through group facilitation. You will contribute to the overall performance and delivery of a responsive, high-quality service, ensuring that all interventions meet clinical governance and IAPT quality standards. You will also actively participate in case management and line management supervision and support the wider team to deliver excellent outcomes. Key Responsibilities • Conduct comprehensive assessments, including risk assessments of self-harm and harm to others. * Deliver a range of Step 2 low-intensity psychological interventions, both individually and in group settings. * Monitor and evaluate outcomes to ensure interventions are evidence-based and effective. * Work collaboratively within a multidisciplinary team to meet service targets and performance standards. * Participate in supervision, training, and continuous professional development. * Support the service to maintain data accuracy and meet reporting deadlines. * Work flexibly across sites to meet the needs of the service and clients About You You will be a compassionate, motivated practitioner with a strong commitment to supporting people in achieving lasting positive change. You'll have a sound understanding of the IAPT model and the principles of stepped care, along with excellent communication and interpersonal skills. Essential Criteria: • Experience delivering Step 2 psychological interventions. * Experience undertaking comprehensive risk assessments. * Thorough understanding of the IAPT model and stepped care. * Strong interpersonal skills and the ability to engage with a diverse range of people. * Genuine interest in motivating and supporting others. * Understanding of the need for evidence-based psychological interventions. * Ability to work flexibly and across multiple sites as required. Desirable Criteria: • Strong project and time management skills. All prison-based roles are subject to enhanced DBS checks and HMPPS security vetting. These checks can take up to 5 months to complete. Any offer of employment will be conditional upon the successful completion of both checks. Please note if you have lived overseas within the last 5 years then checks may take longer. About Us We are The Forward Trust, the social enterprise with charitable status that empowers people to break the often interlinked cycles of crime and addiction to move forward with their lives. For more than 25 years we have been working with people to build positive and productive lives, whatever their past. We believe that anyone is capable of lasting change. Our services have supported thousands of people to make positive changes and build productive lives with a job, family, friends and a sense of community. We are committed to our cause and the work we carry out as a charity. Equally the wellbeing and the employees who work for us are also important. Joining us an employee, we will offer you the following benefits: • Flexible working * Training and development opportunities * Simply Health Cashback Scheme (optional) * Season Ticket Loan Scheme * Cycle to work scheme * Crisis Loan Scheme * Electric Car Scheme * 3 x Wellbeing Days (pro rata'd for part time employees) * Access to Blue Light Card * 25 days (rising to 30 with length of service) Annual Leave plus Bank Holidays * Contributory Pension Scheme - Employer matched contributions of up to 6% in the first two years' service and up to 9% thereafter * Death in Service Payment (2x annual salary) * Critical Illness Insurance (subject to qualifying criteria) To Apply If you feel you are a suitable candidate and would like to work for Forward Trust, please proceed through the following link to be redirected to our website to complete your application.

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

The Senior Data Manager brings advanced understanding of the clinical data management process from study start-up through database lock, including database design and data validation as per the requirements in the clinical study protocols, data review plan, & data management plan, and oversees the c

Experience with consent processes and data collection in clinical research settings. We are looking for a dedicated and passionate Band 5 Clinical Research Nurse to support inpatient I. D clinical research studies on a one-year fixed-term contract.

They seek qualified analysts to support data analytics, develop data products, and improve operational efficiency. A healthcare solutions company is expanding its Clinical Informatics team in the United Kingdom.

A leading healthcare consultancy is seeking a Clinical Data & Evidence Analysis Lead to drive high-impact projects that shape the future of healthcare. In this role, you will evaluate clinical and scientific data related to Medical Device products, influencing marketing claims and regulatory complia

We are hiring a Senior Data Scientist (Clinical Data Analytics) to play a central role in the analysis and interpretation of clinical data collected from in-vivo testing of our device. Help establish and evolve methodologies and best practices for clinical data analysis as the company’s clinical p

This role offers diverse specialty rotations and the chance to develop skills in clinical pharmacy practice.

A Primary Care Network in Solihull is looking for a proactive Projects Support Officer to enhance the delivery of clinical and contractual projects. The role involves maintaining data quality, coordinating various projects, and supporting operational teams.

This role involves analyzing and interpreting clinical data to enhance device performance insights. A leading health technology company in the United Kingdom is looking for a Senior Data Scientist. You'll collaborate across teams to communicate findings effectively, ensuring data quality and perform

In this senior role, you will lead the delivery of high quality clinical pharmacy services across our hospital sites, providing expert clinical input and ensuring safe, effective and patient centred medicines optimisation. Are you ready to take the next step in your clinical pharmacy career and lead

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 global clinical research organization is seeking a Senior Clinical Data Manager to lead data management services across multiple complex projects. The ideal candidate will have at least 5 years of experience in clinical data management, positive analytical skills, and a degree in a life science. T

A global medical communications firm in the UK is seeking Analysts and Medical Writers to work on clinical trial data analysis and presentation. The role involves collaborating with clients and stakeholders to ensure effective communication of scientific data.

A global biopharmaceutical company in the UK is seeking a Senior Manager, Data Management to lead clinical data management for multiple studies. Key qualifications include a Bachelor's degree in a science discipline and 6+ years in clinical data management. The successful candidate will oversee outs

A leading clinical research organization seeks a Senior Data Manager to oversee the clinical data management process. The ideal candidate has extensive experience with RAVE and clinical trials, along with a Bachelor's degree in relevant fields. This role includes leading data management activities,

A healthcare organization is seeking a Clinical Nurse Specialist to join their hepatology team at St Marys Hospital. This role focuses on providing expert care for patients with viral hepatitis, offering clinical advice and managing care autonomously. Ideal candidates will have a nursing qualificati

A leading clinical data management provider in the United Kingdom is seeking a Lead Clinical Data Manager to oversee data management study activities and ensure deliverables are met with high quality. This position requires proven experience in clinical data management, particularly with RAVE, and a

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

Work cross‑functionally to ensure data quality in each database and timely delivery of other data‑management deliverables. Represent the data management function on the Clinical Sub‑team, aligning expectations between CRO and client for all data‑related deliverables, especially regulatory su

A leading clinical research organization is seeking a Senior Clinical Data Science Lead to manage clinical data for trials. This role involves developing data management strategies, collaborating with teams, and ensuring data quality. Candidates should possess an advanced degree in a relevant field

This role focuses on developing AI applications to enhance clinical trial operations and digital healthcare initiatives. A leading global biopharma company is seeking an Associate Director, AI Data Scientist to innovate healthcare solutions.

A leading biopharmaceutical company is seeking a Senior Manager, Data Management to lead clinical data management for multiple studies. The ideal candidate has over 6 years in clinical data management with advanced knowledge of EDC systems, project management, and excellent communication skills. Res

This role involves managing care pathways for research volunteers, collecting data, and collaborating closely with clinical teams. A prominent healthcare facility in Greater London is seeking a Band 5 Clinical Research Nurse to join their multidisciplinary team.

A healthcare communications firm is seeking a Medical Copywriter to create compelling and compliant content that transforms complex clinical information into engaging copy.

A leading pharmaceutical company in the United Kingdom is seeking a Senior Clinical Data Manager. The role involves leading data management activities, utilizing RAVE for electronic data capture, and ensuring high-quality deliverables in collaboration with stakeholders. The ideal candidate will have

A leading medical institution in Greater London is seeking a Senior Clinical Trial Administrator to support clinical research operations. The role involves ensuring compliance with GCP and assisting in study administration, data management, and project coordination. Candidates should have clinical r

A leading pharmaceutical company in the United Kingdom seeks an Analytical Data Science Programmer to transform statistical analysis plans into high-quality programming deliverables for clinical studies. Ideal candidates hold a relevant degree, possess strong programming skills in SAS and R, and dem

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

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.

Senior Clinical Data Manager - US/UK - Remote page is loaded## Senior Clinical Data Manager - US/UK - Remoteremote type: Remotelocations: Durham, North Carolina: England, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: JR101727Who we areWe’re a global,

Are you ready to lead high‑impact projects that shape the future of healthcare? We're looking for a highly skilled Clinical Data & Evidence Analysis Lead to drive commercial success through robust scientific and clinical evidence. Lead - Clinical Data & Evidence Analysis. In this pivotal role, you

Works cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables. Represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and client for all data related deliv

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

A leading healthcare provider in Greater London is seeking a Data Administrator to manage data entry for clinical trials. The role requires attention to detail and compliance with Good Clinical Practice. The candidate will ensure high-quality data management across multiple sites.

Proficiency with MS Excel and a proven ability to manipulate data (V-Look Ups, Pivot Tables) and an ability to learn required business applications. For more information about this HR Data Specialist role, please contact the Key Accounts Team on (phone number removed) or email (url removed). CK Grou

A global clinical data solutions provider is seeking a Senior Data Manager to lead clinical data management efforts. Applicants must possess at least 6 years of experience in Clinical Data Management, including a minimum of 3 years in a leadership capacity. This role involves overseeing all data man

Demonstrated in‑depth understanding of clinical trial data management concepts, processes, and procedures, as well as relevant issues related to or impacting clinical data management and pharmaceutical clinical trial regulations, industry guidance, conventions and standards. At least five years of

This role involves managing data entry for a variety of clinical trials, ensuring compliance with Good Clinical Practice and maintaining high standards of data quality. Ideal for candidates with experience in clinical data management, this role supports innovation in patient care and clinical resear

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

In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations. You will be responsible for the full cycle of Clinical Data Management queries, from being in full leadership of your own studies and

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.

This role focuses on providing technical support for clinical documentation projects, developing training programs, and optimizing processes. Ideal candidates will have strong technical expertise and a background in clinical documentation.

A leading NHS Trust in London is seeking a Lead Pharmacist for Clinical Services (Band 8A) to provide expert clinical input and lead high quality pharmacy services.