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How about working for an employer who has been awarded a ‘Great Place to Work’ for the 5th year running?\nJob Title: Psychotherapist\nLocation: Longdon Park School – Derbyshire DE65 6GU\nSalary: Up to £52,000 FTE DOE\nHours: 15 hours per week, 2 days a week, days to be confirmed\nContract: Permanent – Term Time only\nEssential: Full valid UK driving licence and access to own vehicle\nAbout the role\nWe are looking for an experienced Psychotherapist to join our developing Clinical Team based at Longdon Park School.\nIn this exciting role, you will work collaboratively to deliver bespoke assessment, and intervention plans for pupils with complex communication needs, autism and associated learning and emotional needs.\nYou will implement a holistic, therapeutic approach to helping our pupils in their daily lives, ensuring they are safe, comfortable and healthy. Undertaking all aspects of Psychotherapy clinical duties, you will adhere to professional and regulatory guidelines, carrying out specialist individual assessments and interventions, and preparing relevant documentation, including writing reports. A significant element of this role will be working alongside the onsite clinical team to continue to develop the clinical service provision, including providing support and training to staff and parents.\nOur well-established multidisciplinary Clinical Team maintain a nurturing environment where our pupils can flourish, always putting them at the forefront of everything they do. All our settings maintain a strong safeguarding culture, and our pupils are heard, respected and involved in decisions that affect them wherever possible.\nWhen it comes to looking after our pupils we strive for excellence, which is why we are the leading service provider in the UK. With this in mind, we are looking for a Psychotherapist who shares our vision; to build incredible futures by empowering vulnerable people in the UK to be happy and to make their way in the world.\nLocation: Longdon Park School – Derbyshire DE65 6GU\nLongdon Park School\nAbout the Group\nOutcomes First Group is the largest independent provider of special needs education. We are a vital part of local communities in England, Scotland and Wales with a renowned reputation for quality and positive outcomes for the people we educate for.\nWe are really proud to say that in 2024, Outcomes First Group were officially certified as a ‘Great Place to Work’ for the fifth year running.\nOur divisional brands include Acorn Education and Options Autism.\nFor more information on the group please visit: \nEssential Criteria:\nDegree qualification in specific discipline. Level 7.\nRegistered member of one or more of the following bodies: HCPC, BACP, BABCP, PTUK, NCPC, UKCP\nClear and concise report writing relating to clinical and research activities\nExperience of working with people with neurodivergence and/or complex needs (e.g., complex trauma, neurodevelopmental differences, mental health needs)\nAbility to work independently as agreed under supervision\nExperience of multi-professional work teams or services within designated speciality\nEvidence of continuing professional development relevant to the setting\nFull valid UK driving licence and access to own vehicle\nWhat’s in it for you?\nYou will be working with an ambitious and driven service that’s really going places, supported by an exceptional team of likeminded individuals who are keen to learn from you. You will have the resources and time to implement your strategic vision for therapies as this role will be key to the development of the service. This is an opportunity to enrich the lives of people and make a positive difference, in a role where you have autonomy.\nWe offer a friendly and inclusive working environment where our people are heard, respected and hugely valued. We want our employees to come to work with energy, determination and most importantly we want them to be happy in their work. We are well aware that it is our highly skilled teams that make Outcomes First Group the success it is, and we want this to continue. This is why we provide a range of benefits designed to support you, not just in your work life but also on a personal level too. We want you to be the best you can be and offer genuine opportunities for career development and progression.\nBenefits and Rewards\nProfessional support network\nContributory Pension\nEmployee Rewards Hub – access to discounts, offers and cashback with 100s of retailers\nCareer pathways and a dedicated learning and development team\nThe Hub – employee discounts, recognition cards, well-being centre\nCycle to Work scheme\n“Your Wellbeing Matters” Programme\nEmployee Assistance Programme\nSalary Finance\nFlexible benefits scheme that allows you to adjust your benefits to suit you.\nFamily Growth Support - inclusive benefits package covering enhanced maternity and paternity leave, along with paid fertility treatment support.\nFor further information on this role please refer the Job Description and Person Specification attached. To discuss this role in more detail, please contact: \nAt Outcomes First Group we are committed to the safeguarding and promoting the welfare of our pupils and young people. All successful applicants will be subject to social media checks and successful applicants to a fully enhanced DBS\nWe reserve the right to close vacancies early if we receive a high volume of suitable applicants.\nOutcomes First Group is committed to carrying out a fair, thorough and efficient recruitment process in line with Keeping Children Safe in Education. Whilst we aim to keep applicants informed throughout, Outcomes First Group does not accept liability for any loss of earnings or other associated costs incurred by applicants as a result of delays or changes in the compliance process. All stages of the compliance process are subject to necessary safeguarding checks and compliance with statutory requirements, which may affect timescales.\nVacancy ID 292346\n#1

Now accepting applicants for Focus Group studies. Earn up to £700 per week part-time working from home. Must register to see if you qualify. No Customer Service Representative Agent experience needed. Customer Service Representative Agent Work From Home - Part Time Remote Focus Group Panelists Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments. With most of our paid focus group studies, you have the option to participate remotely online or in-person. This is a great way to earn additional income from the comfort of your home. Compensation: £55 - £120 (per 1 hour session) £250 - £700 (multi-session studies) Job Requirements: Show up at least 10 mins before discussion start time. Participate by completing written and oral instructions. Complete written survey provided for each panel. MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date. Qualifications: Must have either a smartphone with working camera or desktop/laptop with webcam Must have access to high speed internet connection Desire to fully participate in one or several of the above topics Ability to read, understand, and follow oral and written instructions. Customer service representative agent experience is not necessary. Job Benefits: Flexibility to take part in discussions online or in-person. No commute needed should you choose to work from home remotely. No minimum hours. You can do this part-time or full-time Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products. You get to review and use new products or services before they are released to the public. You must apply on our website and complete a set of questionnaire to see if you qualify. This position is perfect for anyone looking for temporary, part-time or full-time work. The hours are flexible and no previous experience is required. If you are a customer service representative agent or someone just looking for a flexible part time remote work from home job, this is a great way to supplement your income.

Now accepting applicants for Focus Group studies. Earn up to £700 per week part-time working from home. Must register to see if you qualify. No Customer Service Representative Agent experience needed. Customer Service Representative Agent Work From Home - Part Time Remote Focus Group Panelists Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments. With most of our paid focus group studies, you have the option to participate remotely online or in-person. This is a great way to earn additional income from the comfort of your home. Compensation: £55 - £120 (per 1 hour session) £250 - £700 (multi-session studies) Job Requirements: Show up at least 10 mins before discussion start time. Participate by completing written and oral instructions. Complete written survey provided for each panel. MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date. Qualifications: Must have either a smartphone with working camera or desktop/laptop with webcam Must have access to high speed internet connection Desire to fully participate in one or several of the above topics Ability to read, understand, and follow oral and written instructions. Customer service representative agent experience is not necessary. Job Benefits: Flexibility to take part in discussions online or in-person. No commute needed should you choose to work from home remotely. No minimum hours. You can do this part-time or full-time Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products. You get to review and use new products or services before they are released to the public. You must apply on our website and complete a set of questionnaire to see if you qualify. This position is perfect for anyone looking for temporary, part-time or full-time work. The hours are flexible and no previous experience is required. If you are a customer service representative agent or someone just looking for a flexible part time remote work from home job, this is a great way to supplement your income.

Company: Medical Devices (Start Up).My client is looking for an experienced Medical device CRA to join their team in the UK as they ramp up their study towards the back end of the year.This is direct with the company - so prior direct medical device CRA experience is required to be considered for th

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Precision’s uniquely integrated offering enables the science of precisi

A fast-growing, tech-enabled CRO and global site network that started life within a major biopharma before becoming fully independent.India, and plans for Brazil, Australia, and China.It’s a genuine startup culture — everyone contributes, collaborates, and grows together.You’ll monitor sites a

Join a highly experienced team dedicated to excellence in clinical research. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;. Prepare accordingly and attend investigator meetings, coordina

Are you an accomplished Clinical Research Associate seeking a stimulating and pivotal career move? Do you excel in a culture where quality site engagement is prioritised over rigid metrics and where your well-being is a core value? This is the chance to join a clinical research organisation with a s

Job Title: Lead Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research. Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug

Study: Study on medical device.Monitoring Visit On site (MOV).A person with experience also in regulatory submission is appreciated.

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Precision’s uniquely integrated offering enables the science of precisi

Are you an accomplished Clinical Research Associate seeking a stimulating and pivotal career move? Do you excel in a culture where quality site engagement is prioritised over rigid metrics and where your well-being is a core value? This is the chance to join a clinical research organisation with a s

Minimum 3 years of experience coordinating Phase 2–4 clinical trials in a site, SMO, or academic research setting. Certified Clinical Research Coordinator (CCRC) a plus. At Civia Health, our Clinical Research Coordinators are essential to deliver trials that are efficient, ethical, and patient-cen

Are you an accomplished Clinical Research Associate seeking a stimulating and pivotal career move? Do you excel in a culture where quality site engagement is prioritised over rigid metrics and where your well-being is a core value? This is the chance to join a clinical research organisation with a s

Clinical Research Associate II/Senior Clinical Research Associate. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. We com

Are you an accomplished Clinical Research Associate seeking a stimulating and pivotal career move? Do you excel in a culture where quality site engagement is prioritised over rigid metrics and where your well-being is a core value? This is the chance to join a clinical research organisation with a s

Be part of a forward-thinking team driving excellence in clinical research. MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. MAC Clinical Research is seeking a highly experienced and innovative.

Support the delivery of a high quality and flexible laboratory service in support of various clinical research projects. We are an experienced team with dedicated research specific laboratory staff, currently consisting of 1 Associate Practitioners who, under the supervision of the Biochemistry Mana

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. Solution Architect - Clinical Data Warehouse. Solution Architect – Clinical Data Warehouse.

Clinical Research Associate II/Senior Clinical Research Associate. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. We com

Every team member plays a crucial role in reshaping clinical research. Certified Clinical Research Coordinator (CCRC) a plus. Minimum 3 years of experience coordinating Phase 2–4 clinical trials in a site, SMO, or academic research setting.

Join a highly experienced team dedicated to excellence in clinical research. Senior Clinical Research Associate, west midlands. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;.

As part of a pool, provide personal administration / diary management for five members of the Clinical Research Directorate senior management team (Director of Clinical Research Operations, Head of Clinical Research Performance and Quality, Head of Clinical Research Delivery, Head of Investigator In

Senior Clinical Research Associate page is loaded## Senior Clinical Research Associatelocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: December 25, 2025 (30+ days left to apply)job requisition id: R1510425Join Us on Our M

Provision of medical care and oversight of clinical trial participants in Neuroscience/Adult Psychiatry/Old Age Psychiatry/Psychedelic clinical trials. We are seeking to appoint Clinical Research Physician/SAS Speciality Psychiatrist Doctors to join our dedicated team in Blackpool, Lancashire. The f

We are an experienced team with dedicated research specific laboratory staff, currently consisting of 1 Associate Practitioner who, under the supervision of the Biochemistry Manager, offers laboratory assistance to a range of research studies across York and Scarborough Hospitals. Experience in supp

At least 5 years’ experience as a Clinical Research Associate with a sound track record in managing clinical trial site. Senior Clinical Research Associate (UK) – Theradex Oncology. Senior Clinical Research Associate (UK).

Prepare for and attend investigator meetings; coordinate delivery and storage and accountability of clinical supplies; follow up on drug safety issues. Principal Recruitment Consultant | Clinical Operations | Global Recruitment. Conduct feasibility, pre-study, initiation, monitoring, and closeout vi

You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team.This includes work related to regulatory affairs, site activation processes—including contracting and start-up activities—to ensure smooth and compliant study exec

Background in Clinical Research is preferred. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies.

Clinical Research Associate II/Senior Clinical Research Associate – Remote, United Kingdom. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regula

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. Parexel is seeking Clinical Research Associates home-based in South West England to cover trials in the region. Working as a Clinical Research Assoc

Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. Assesses factors that might affect subject/patient's safety and clinical data integrity at an

Support the development of ABPI’s policy work to enhance the UK's clinical trials environment, streamline industry access to research infrastructure, demonstrate the international standing of the UK’s clinical trials offering, and develop collaborations with funders, academia, charities, and res

Senior Clinical Research Associate, bedford. Join a highly experienced team dedicated to excellence in clinical research. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year.

CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study miles

Are you an experienced clinical pharmacologist or physician researcher with a passion for early phase research? The GSK Clinical Unit Cambridge (CUC) is seeking a. The CUC operates within the Early Pipeline Unit of GSK’s Respiratory, Immunology and Inflammation Research Unit and operates as a glob

Checks the site and external facilities, equipment, and supplies (clinical and non-clinical) continue to be adequate to conduct the trial and with their expiry dates (as applicable). REGISTER YOUR INTEREST FOR UPCOMING ONCOLOGY FOCUSED SENIOR CLINICAL RESEARCH ASSOCIATE OPPORTUNITIES. Parexel are cu

The Clinical Research Associate will support the delivery of clinical studies by monitoring study sites, ensuring data quality, and maintaining compliance with study protocols and regulatory requirements. A motivated early-career Clinical Research Associate with a passion for high-quality study deli

Acts as a leader driving global study and/or program clinical team and departmental engagement, maximizes the efficiencies of the clinical team across studies/program. Oversight of financial health of clinical activities including support with identifying out-of-scope tasks from the Premier clinical

CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Senior Clinical Research Associate. Collaborates with Regional Clinical Operations Manager and clinical study sites to e

Join a highly experienced team dedicated to excellence in clinical research. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, inc

Clinical Research Associate II (United Kingdom). Clinical Research Associate (CRA II). As a CRA II at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and

As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials. Next generation clinical deve

Clinical Research Associate II (United Kingdom) at Allucent. As a CRA II at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs,

The Clinical Research Associate will support the delivery of clinical studies by monitoring study sites, ensuring data quality, and maintaining compliance with study protocols and regulatory requirements. KEMIO Consulting is excited to be partnering with a medium-sized well-established CRO looking t

They will manage their own caseload of patients on clinical trials with the support of the wider research and clinical team. You will take responsibility for the co-ordination and management of a clinical research portfolio, collaborating with key personnel to ensure continued care and support for p

The post holder will support the aims of the Trust and the NIHR clinical research network to improve the speed, quality, and integration of clinical research, through the successful delivery of clinical research in the NHS. You will work collaboratively with the research teams and the wider multidis