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As a Relief Counsellor, you will provide therapeutic counselling to individuals accessing CrossReach Counselling Services. Working as part of a supportive and professional team, you will help ensure clients receive a high quality, compassionate service that supports wellbeing, resilience and personal growth. This flexible relief role allows you to contribute your professional skills within an established counselling service committed to strong clinical standards and person centred care. What your day could look like • Providing therapeutic counselling using an appropriate recognised theoretical model, • Holding clinical responsibility for your own caseload from referral through to completion of therapy and evaluation, • Maintaining accurate and confidential therapeutic records using approved systems, • Working closely with clinical and business support colleagues to ensure coordinated care, • Attending and contributing to clinical and management supervision, • Working in line with safeguarding, data protection and professional ethical standards, • Liaising with other professionals where safeguarding concerns arise, • Supporting service improvement through reflective practice and shared learning, • Maintaining your continuing professional development and keeping up to date with current research and best practice About you You will hold a Diploma in Counselling or another relevant qualification such as Art Therapy and be registered with PSA or HPC. A qualification in counselling for Children and Young People is desirable but not essential. You will have significant post qualifying practice hours and the ability to manage your own caseload while working effectively within a multidisciplinary team. You will bring strong communication skills, sound professional judgement and the ability to maintain appropriate boundaries and ethical practice. Good IT skills are required, including the ability to use Microsoft Office and online systems to maintain accurate records. You will value supervision and reflective practice, demonstrate strong self awareness and take responsibility for maintaining your own professional wellbeing. You must be respectful of the Christian ethos of CrossReach and able to work within it. This role requires membership of the Protecting Vulnerable Groups (PVG) Scheme and completion of the necessary vetting checks. What you will gain • Flexible relief work within an established counselling service, • Regular supervision and professional support, • Opportunities for continuing professional development, • The opportunity to contribute to a service that supports people through challenging life experiences If you are a qualified counsellor looking for flexible work where your professional skills can make a meaningful difference, we would welcome your application. Apply today. CrossReach has been at the forefront of high quality social care for over 150 years, providing loving care to people of all ages and supporting them to live life to the full whatever their circumstances. During that time, we have worked hard to understand the needs of the people who turn to us for help and with them have been at the forefront of pioneering services which have literally changed thousands of lives for the better. Today we are one of the largest social care providers in Scotland, with experience across a broad range of services. We are still growing, learning, and improving, thanks to the incredible people we have the privilege to support, and all those who support us. We are part of the Church of Scotland and aim to provide social care services and specialist resources in Christ’s name to further the caring work of the Church to people in challenging circumstances. As we do our work in Christ’s name you must be respectful of our Christian Ethos and be able to work within it. This post requires you to be a member of the Protecting Vulnerable Groups (PVG) Scheme and undertake the necessary vetting checks. You will also be required to be registered with SSSC and it is your professional responsibility to ensure that you meet the standards and criteria for registration. We have a legal obligation to ensure that we do not employ any worker who has not been granted the relevant permission to work in the UK. This permission is without exception granted by UK Visas and Immigrations. We are required to check the entitlement to work in the UK of all prospective employees, regardless of nationality or job category. We are committed to ensuring that we attract, retain, and develop the very best people to build a diverse and talented team and we recognise that every individual’s unique background, experience and ability contributes to our success. We aim to create an inclusive and inspiring environment where individuals feel valued and respected and where people can belong, thrive and be their very best, whoever they are. If you have any queries regarding this role or our recruitment process, please contact the Recruitment team on Please note: We reserve the right to close this advert prior to the closing date. Therefore, please make sure you complete and submit your application at an early stage. ADDITIONAL INFORMATION FOR CANDIDATES • Application Process: Please apply for this post by completing the application process on Jobtrain. You can find out more about our recruitment process CrossReach Recruitment Process, • CV Upload: DO NOT upload a CV as this will not be used for shortlisting purposes., • Deadline: Posts close at midnight on the indicated date., • Application Assistance: For help completing an application on Jobtrain, please click here - Application Guidance - Jobtrain, • To view our accessibility statement, please click here. CrossReach Accessibility Statement, • Communication: Please note that most of our communication is via email; therefore, please ensure you enter your email address accurately and ensure that “Jobtrain” and “CrossReach” are marked as safe email address. However, we will at times also call you or send you a text message., • Check Email Regularly: Please check your email regularly (including junk folders) and also your Jobtrain account for updates., • Support Hub: For advice and support with any system issues, please contact Jobtrain Candidate Support Hub - Jobtrain - Jobseekers Support Hub, • Browser Recommendation: We recommend using the internet browsers "Google Chrome" or "Microsoft Edge" when using Jobtrain., • Amendments: Once you have submitted your application form, you will be unable to make any amendments.

Phlebotomists / HCAs Needed – Greater Edinburgh Mobile sites across the Lothians Up to £19 per hour (umbrella) + weekend enhancements Starting April | Ongoing project Pulse AHP’s Phlebotomy Team is recruiting experienced Phlebotomists / Healthcare Support Workers to support an established health research programme as it moves into its next phase. This is a flexible, shift-based role (similar to bank work), ideal if you’re looking for part-time hours or a second role. We’re looking for candidates who can commit to at least 2 days per week within a 7-day service. The Role You’ll be working on mobile research units across the Greater Edinburgh area (locations rotate every 5–6 weeks), supporting participants through: • Venepuncture (2 blood samples per participant), • Height, weight & waist measurements, • BP and heart rate checks, • Data input onto clinical systems, • Participant welfare checks and escalation where needed, • Preparing samples for courier collection Essential Requirements • Minimum 12 months recent phlebotomy experience, • HCA / clinical support experience, • Ability to work 2–3 days per week, • Willingness to register fully with Pulse, • Driving licence highly beneficial due to mobile sites Expected locations over coming months Dalkeith | Livingston | Whitburn (and surrounding areas) Please advise if you would be interested in this vacancy

Principal Cybersecurity Test Engineer Location: Edinburgh, Scotland Company: Spacelabs Healthcare Employment Type: Full-Time, Permanent About Spacelabs Healthcare At Spacelabs Healthcare, we are on a mission to provide continuous innovation in healthcare technology for better clinical and economic outcomes. Our scalable solutions deliver critical patient data across local and remote systems, enable better-informed decisions, increase efficiencies, and create a safer environment for patients. Why work at Spacelabs? Because lives depend on you! Job Summary The Principal Cybersecurity Test Engineer is an elite-level individual contributor role within the Spacelabs Cybersecurity Team. This position is responsible for designing and conducting penetration testing to ensure robust security controls for Spacelabs products, infrastructure, and solutions. Key Responsibilities • Design and execute penetration tests simulating advanced cyber threat tactics and techniques., • Research emerging threats, vulnerabilities, and attacker methodologies using internal and external resources., • Develop and maintain security assessment project plans., • Create and implement security exploits for penetration testing; continuously adopt new exploit development methods., • Evaluate applicability of exploits and tools for products and applications., • Support security awareness initiatives and product investigations for complaints/incidents., • Participate in requirement reviews, team meetings, and company-wide security knowledge-sharing activities., • Perform code reviews, integration testing, and implement fixes for software defects and change proposals., • Document test plans, scenarios, findings, and recommendations in detailed penetration test reports., • Provide regular progress updates and conduct technical reviews of test activities and results. Qualifications Domain Expertise • Deep understanding of firmware, operating systems, applications, networks, encryption algorithms, and access control models., • Proficiency in coding languages: Assembly, C, C++, Java, C#, .NET, Python., • Expertise in operating systems (Linux, Windows), databases (MS SQL, MySQL, Postgres), and application/web servers (Apache, IIS, Wildfly)., • Strong networking knowledge (switching, routing, firewalls) and hardware hacking (JTAG, FPGA, USB)., • Experience with security testing tools: Kali Linux, Nessus, Metasploit, BurpSuite, Wireshark, etc., • Familiarity with secure coding practices (OWASP), SDLC, and security frameworks (ISO 2700x, NIST)., • Self-motivated, strong problem-solving and analytical skills., • Excellent communication and teamwork abilities., • Bachelor’s degree with 12+ years of related experience OR Master’s degree with 10+ years of related experience., • Degree in Computer Science, Cybersecurity, Software Engineering, or related technical discipline.

About the Company:My client is a fast-growing start-up in the MedTech industry, dedicated to developing innovative solutions that make a difference in patient care and outcomes. About the Role: The Business and Clinical Operations Support Officer will provide high-level administrative support to the COO, Head of Clinical Operations and wider team, ensuring the smooth day-to-day running and efficient coordination of key business and clinical activities. The role will also provide administrative support to Clinical Operations, including formatting and version control of key documents, maintaining study trackers and coordinating meetings. This position requires excellent organisational skills, strong attention to detail, and the ability to follow procedures and manage multiple priorities effectively. The ideal candidate will be a proactive self-starter with a can-do attitude, strong communication skills, and the ability to work independently while following established processes, regulatory procedures and instructions where required. Responsibilities: • Executive Business Support: Assist the team with daily administrative tasks, including managing calendars, scheduling meetings, preparing reports, and organising travel arrangements., • Meeting Coordination: Coordinate and schedule meetings, conferences, and appointments as needed. Prepare agendas, take meeting minutes, and follow up on action items., • Document Management: Draft, edit, and proofread documents, presentations, and spreadsheets. Maintain and organise important company files and records in a secure and efficient manner., • Office Operations: Assist in managing office supplies, equipment, and vendor relationships. Support the team with occasional event planning and office logistics., • Special Projects: Assist the team with various projects, research tasks, and data analysis as required. Provide support for strategic initiatives and new business opportunities., • Confidentiality: Maintain the highest level of confidentiality and handle sensitive information with discretion and professionalism., • Clinical Operations Support: Provide administrative assistance, including formatting and managing version control of documents, maintaining trackers and logs, organising and filing documentation, coordinating meetings, taking minutes, and ensuring accurate and up-to-date record-keeping. Qualifications: • Experience: Minimum 5 years of experience in an administrative or executive assistant role, preferably in a startup or fast-paced environment, or 2 years plus a degree in a relevant area., • Experience supporting clinical operations, healthcare, MedTech, or regulated environments is desirable but not essential. Education: • Higher grade Maths and English or equivalent required. Required Skills: • Strong organisational and time management skills, with the ability to prioritise tasks effectively., • Excellent written and verbal communication skills., • Reliable, methodical, comfortable following processes, and able to work under guidance in a regulatory environment., • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with collaboration tools like Google Workspace, Teams, and Zoom., • Ability to work independently and take initiative, while also following instructions carefully., • Excellent attention to detail with a strong focus on accuracy and quality., • Tech-savvy and adaptable to new software and systems. Preferred Skills: • Experience supporting clinical operations, healthcare, MedTech, or regulated environments is desirable but not essential. Pay range and compensation package: • Competitive salary based on experience., • Opportunities for professional growth and development., • Flexible work environment, with the option for occasional remote work., • A collaborative and innovative team culture. Equal Opportunity Statement: Our client is an equal opportunity employer. They celebrate diversity and are committed to creating an inclusive environment for all employees.

Phlebotomists / HCAs Needed – Greater Edinburgh Mobile sites across the Lothians Up to £19 per hour (umbrella) + weekend enhancements Starting April | Ongoing project Pulse AHP’s Phlebotomy Team is recruiting experienced Phlebotomists / Healthcare Support Workers to support an established health research programme as it moves into its next phase. This is a flexible, shift-based role (similar to bank work), ideal if you’re looking for part-time hours or a second role. We’re looking for candidates who can commit to at least 2 days per week within a 7-day service. The Role You’ll be working on mobile research units across the Greater Edinburgh area (locations rotate every 5–6 weeks), supporting participants through: • Venepuncture (2 blood samples per participant), • Height, weight & waist measurements, • BP and heart rate checks, • Data input onto clinical systems, • Participant welfare checks and escalation where needed, • Preparing samples for courier collection Essential Requirements • Minimum 12 months recent phlebotomy experience, • HCA / clinical support experience, • Ability to work 2–3 days per week, • Willingness to register fully with Pulse, • Driving licence highly beneficial due to mobile sites Expected locations over coming months Dalkeith | Livingston | Whitburn (and surrounding areas) Please advise if you would be interested in this vacancy

A top-ranking university in Edinburgh is seeking an ambitious Obstetrics and Gynaecology trainee for a prestigious three-year Clinical Lectureship. This role offers a unique opportunity to blend high-quality specialist training with protected research time. The position demands strong clinical exper

A leading healthcare provider in Scotland seeks a Deputy Director for Research & Development to oversee robust clinical research operations. The role demands a degree and postgraduate qualification in life sciences, alongside in-depth knowledge of research governance.

A leading global provider of clinical research services is looking for a Market Access Manager to lead their access strategy across the UK. The successful candidate will build relationships with key NHS stakeholders and manage tender submissions.

A leading healthcare provider in Edinburgh is seeking a Radiotherapy Team Lead to direct and support a skilled team of Therapeutic Radiographers. Candidates will be responsible for leading a diverse range of treatments and must be enthusiastic about furthering education and clinical research. The su

A life sciences company in Edinburgh is seeking a Clinical Research Physician to contribute to clinical studies focused on neurodegenerative conditions.

A leading research university in Edinburgh is looking for a Graduate Research Practitioner to support clinical studies focusing on neurological conditions. The position provides opportunities for professional development and includes comprehensive staff benefits, making it an ideal springboard for a

Scottish Brain Sciences is a Life Sciences Company headquartered in Edinburgh, Scotland.We conduct observational research and deliver clinical trials of new treatments for a range of neurodegenerative conditions, including Alzheimer's disease, and we foster the rapid translation of research into pra

Working across mobile research units in the Greater Edinburgh area (locations rotate every 5–6 weeks), you will provide clinical and operational leadership to Healthcare Support Workers and phlebotomy teams, ensuring safe, high-quality service delivery. Phlebotomy & Healthcare Research Programme.

A healthcare provider is seeking a Nursing Service Delivery Lead in Greater Edinburgh.This part-time role involves clinical leadership and supervisory responsibilities for Healthcare Support Workers and phlebotomy teams in a mobile research environment.Candidates should possess a Registered Nurse qu

CIRG offers a wide base of Principal Investigators with a broad range of research areas, giving the fellow opportunity for self‑direction and development of work related to their interests.

Join the Future of Clinical Research | CRA I & II (FSP). Clinical Research Associates (CRA I & II). If you perform, you progress, with defined tracks into Senior CRA, Lead CRA, and Clinical Project Management.

I am currently looking for a Director or Senior Director of Business Development for a fantastic global full service clinical Contract Research organization with a great culture and excellent proposition. Engaging with internal research staff to maximise selling opportunities associated with existin

Pulse AHP's Phlebotomy Team is recruiting experienced Phlebotomists / Healthcare Support Workers to support an established health research programme as it moves into its next phase. Essential RequirementsMinimum 12 months recent phlebotomy experienceHCA / clinical support experienceAbility to work 2

Clinical Data Manager (12 Month FTC) - Edinburgh Hybrid Lorien's long-standing, successful and very impressive client, with a great global-reaching product line and offices very commutable from Central Edinburgh, Fife, West Lothian and the surrounding, is looking to recruit a Clinical Data Manager on a 12-month fixed term contract basis who can bring a proven track record in the domain and skills across the following to the table. The Clinical Data Manager position is an integral part of the Clinical team, responsible for providing comprehensive data management support to ongoing studies and projects. As the Clinical Data Manager, you will be tasked with ensuring the accuracy, integrity, and timely delivery of clinical data throughout the study lifecycle. Your key responsibilities will include: Overseeing, alongside the Director of this area, all related documentation including developing and maintaining robust Data Management Plans and Data Handling Manuals and setting up and maintaining the Trial Master File Coordinating study and project status updates for relevant meetings Coordinating the development/review of clinical research documents, such as protocols and CRFs Oversee EDC database specification and UAT processes, including test script drafting, eCRF design, edit checks, and validation rules/documentation Performing data quality assessments/reconciliation, query management, and data locking activities Assisting with the preparation of data for statistical analysis and regulatory submissionsWhat they're looking for: Degree in a scientific discipline, as well as a demonstrable track record of clinical data management within a Pharmaceutical/MedTech/similar regulated setting Proficiency in clinical database applications (e.g. EDC/CTMS) Ideally but not necessarily - Programming skills with the likes of SQL and/or Python Strong understanding of GCP and GMP, as well as relevant regulatory requirements and jargon and research/trial processes In addition to these technical skills, you'll demonstrate excellent analytical and problem-solving abilities, strong interpersonal skills with the ability to work with people at any level, and comfort working collaboratively in a global, virtual team environment.This company is known for its commitment to innovation, quality, and customer-centricity. As the Clinical Data Manager, you will have the opportunity to contribute to the development of cutting-edge medical technologies that have a direct impact on peoples' lives the world over. If you are excited about the prospect of being part of a great and evolving organization, we encourage you to apply for this Clinical Data Manager FTC today with your latest CV for immediate consideration. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

A leading clinical research organization in the UK seeks a Clinical Research Associate II for a fully home-based position. The position offers a supportive environment and opportunities to contribute to meaningful clinical research. The role involves monitoring clinical studies, ensuring compliance

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. We are currently recruiting for Clinical Research Associate II to join our Multi-Sponsor Clinical Operations Team in the UK. Your hard work may be rewarded through a bonu

A leading healthcare provider in Scotland is seeking a clinical fellow in General Medicine for a 12-month fixed-term position starting in August 2026.

A clinical research organization is looking for a SAS Programmer III with strong SAS and R skills to support clinical trials remotely in the UK. Candidates should have a Bachelor's degree in a related field and at least 3 years of experience in clinical programming. This is an excellent opportunity

A leading UK university seeks a Clinical Research Data Integration Coordinator to work on cancer research initiatives. This role requires extracting and validating clinical data from medical records, integrating this data into research repositories while ensuring its quality and completeness. The id

A leading research organization is seeking Clinical Research Experts in Chemistry and Biology to work on advanced research problems. Candidates must hold a PhD in Clinical Research or related fields and have strong communication skills. Responsibilities include designing research studies, evaluating

A biopharmaceutical organization in the UK is seeking a Senior Clinical Trial Associate to provide administrative support to clinical teams and maintain clinical documentation. Candidates should have a degree in life sciences or nursing and over 4 years of experience in clinical trial processes.

At least 5 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities

Candidates will collaborate on impactful AI projects, contribute to research publications, and gain professional development.

PhD in Clinical Research, Chemistry, Biology, Biochemistry, Molecular Biology, Pharmacology, or a related field. Expertise in clinical study design, experimental methodology, biochemical or chemical analysis, or translational research. Clinical Research Expert (Chemistry & Biology).

Project Management for our biostatistical services, provide technical supervision and lead project teams in all biostatistical activities of clinical trials. Several years of professional experience (5 - 7 years) in the statistical evaluation of clinical trials in a CRO or the pharmaceutical industr

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 renowned research university in Edinburgh is looking for a Graduate Research Practitioner to join the Anne Rowling Regenerative Neurology Clinic. This full-time, two-year role focuses on clinical research, offering opportunities in data management and patient recruitment for neurological studies.

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate to monitor clinical trials and ensure compliance with regulatory standards.

A clinical research firm in the United Kingdom is seeking a full-time Project Manager in Biometrics. You will oversee biostatistical services, ensuring high-quality management of clinical trials.

Organisation/Company UNIVERSITY OF SOUTHAMPTON Research Field Other Researcher Profile Recognised Researcher (R2) First Stage Researcher (R1) Application Deadline 1 Apr 2026 - 00:00 (UTC) Country United Kingdom Type of Contract Other Job Status Full-time Is the job funded through the EU Research Fra

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. You program and validate statistical analysis of clinical studies with SAS. You are responsible for

A clinical research organization is seeking a dedicated Mobile Research Nurse to support clinical research efforts in Bolton & Manchester. Join our team to make a significant impact in clinical research. The role involves administering investigational medications, conducting patient assessments, and

A leading AI research firm is looking for a Clinical Research Expert in Chemistry & Biology. This remote position involves designing advanced research problems, evaluating experimental frameworks, and generating data to support AI innovations. Responsibilities include collaboration with AI research

A prestigious UK university is seeking an NIHR Academic Clinical Lecturer to offer doctors in specialty training a unique role combining clinical specialty training and academic research. This full-time fixed-term position allows for substantial advancement in clinical academia. Ideal candidates wil

An NHS Trust in the UK is seeking a candidate to join their Urology team, focusing on supporting the middle grade rota and contributing to ongoing research on BPH. Candidates will have opportunities to enhance their clinical and operative skills while working in a dynamic team of 12 consultants.

Make an impact in healthcare - The speed of bringing needed medical innovation to market still depends on the duration of clinical by globally lowering the barrier for access to clinical trials and increasing the chances to find a treatment for patients, we accelerate medical innovation. Clariness i

Ideally, you will have some initial experience in the statistical analysis of clinical studies. You will programme and validate the statistical evaluations of clinical studies using SAS. You will be the point of contact for customers regarding statistical questions in clinical studies.

A leading healthcare provider is looking for a Senior Paediatric Research Nurse to support high-quality nursing care for patients in clinical research. This role includes coordinating studies, managing research data, and delivering nursing care according to Good Clinical Practice guidelines.

As a growth-oriented medium-sized company with over 155 employees, we operate internationally.Our customers appreciate the competence and commitment of our employees and we value our employees as the basis of the company's success.Join a motivated and friendly team as a.Lead the end-to-end setup of

You will be a registered nurse with clinical research experience and current GCP training, able to work independently while contributing effectively within a multidisciplinary team. An exciting opportunity has arisen for a Research Nurse to join Norwich Medical School to support the Norfolk Arthriti

Ideal candidates will have a degree in life science or relevant experience and familiarity with clinical research. An innovative medical research firm in the UK is seeking a Senior Proposals and Pricing Associate.