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We are looking for a Registered Mental Health Nurse (RMN) with a passion for delivering outstanding care. You’ll be working 42 hours a week (Days, Nights and Weekends) at Cygnet Pindar House. Cygnet Pindar House is our 22 bed Neuropsychiatric care and treatment service for men affected by acquired brain injuries. It is a safe and secure place to aid recovery as well as offering those diagnosed with a progressive neurological disease like Huntington’s Disease, a caring and longer term placement to support and help manage the progression of their symptoms. At Cygnet, our perks go way beyond pension schemes and excellent professional development. You’ll also enjoy shopping, travel and leisure discounts – as well as a range of healthcare and financial benefits – to support you to be happy both in and out of work. Apply now to enjoy excellent career prospects while reaping the rewards of making a difference to others – every day. Your day-to-day… • Produce outstanding written reports based on your nursing assessments & observations, • Work closely with the management team to develop the service, audit, & improve quality, • Attend all training and engage in CPD to further knowledge & promote nursing, • Under NMC guidelines, ensure that individual care plans are complete & maintained collectively with residents, relatives & other healthcare professionals, • NHS & employee discount scheme, • Most of our sites provide free meals on shift, • Free parking, • Bespoke career pathways An experienced RMN with a current Pin Number, you’ll have… Essential: • The ability to maintain documentation, undertake audits & demonstrate integrity in your role, • A good understanding of the latest nursing practices, • A commitment to patient recovery in order to effectively monitor, manage & reduce risk, • The ability to deputise in a clinical lead role

Join a highly experienced team dedicated to excellence in clinical research. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly ph

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

Job Title: Lead Clinical Research Associate. 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;.

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

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

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

Clinical Research Associate page is loaded## Clinical Research Associatelocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: November 30, 2025 (30+ days left to apply)job requisition id: R1508089Join Us on Our Mission to Driv

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

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Next generation clinical development!.

Join a highly experienced team dedicated to excellence in clinical research. Key accountabilities Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out); </l

In preparation for your interview, you may feel that you would like to learn more about the National Institute for Health and Care Research and clinical research you may want to look at the following:. Clinical Research Practitioner/Research Nurse. Improving Healthcare Through Clinical Research.

Join a highly experienced team dedicated to excellence in clinical research. Key accountabilities Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out); </l

Background in Clinical Research is preferred. Referrals increase your chances of interviewing at Catalyst Clinical Research by 2x.

Maintain an awareness of the literature on cancer therapy, clinical trial design and conduct, and good clinical practice. Previous experience with Clinical Research Site Coordination or related fields (i. Theradex Oncology is a full-service Contract Research Organization (CRO).

You will work alongside established clinical teams, researchers, research nurses and administrators to facilitate recruitment, sample collection, data entry and providing clinical support as required. Building on our track record of delivering pioneering research we are working in collaboration with

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. Site Coordinators, Clinical Research Coordinators. Medpace is a full-service cl

Our client, an international clinical research organisation (CRO) is currently looking for a Senior Clinical Research Physician to join their team at their state of the art site in London. Strong background in clinical research / clinical trials. As a Senior Clinical Research Physician, you will spe

Clinical Research Associate (Sr. CRA 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, applicable regulations, and the prin

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-centered. Minimum 3 years of experience coordinating Phase 2–4 clinical trials in a site, SMO, or academic research se

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

Organisation/Company KINGS COLLEGE LONDON Research Field Medical sciences Researcher Profile First Stage Researcher (R1) Country United Kingdom Application Deadline 26 Oct 2025 - 00:00 (UTC) Type of Contract Other Job Status Full-time Is the job funded through the EU Research Framework Programme? No

Job Title: Lead Clinical Research Associate. 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.

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

Senior Clinical Research Associate page is loaded## Senior Clinical Research Associatelocations: United Kingdom Remotetime type: Full timeposted on: Posted Yesterdayjob requisition id: R31345BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced p

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

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,

Clinical Research Associate II/Senior Clinical Research Associate. Clinical Research Associate II/Senior Clinical Research Associate. Research Assistant/Clinical Research Coordinator - London London, England, United Kingdom 18 hours ago.

Director, Clinical Operations Real-World and Late Phase Research. Many consider Real-World and Late Phase research as the most significant and growth oriented aspect of clinical development today. The Director, Clinical Operations will play a key role in the continued growth, success and profitabili

Job Title: Lead Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research. Lead Clinical Research Associate, west midlands.

Senior Clinical Research Physician. This position offers significant opportunities for leadership and career development, including the chance to build and mentor a clinical research team and influence sponsor interactions. Provide strategic medical oversight for clinical trials, ensuring protocols

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. Precis

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Next generation clinical development!.

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

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

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 patients involved in clinical trials. They will manage their own caseload of patients on clinical trials with the support of t

Senior Clinical Research Associate, wakefield. 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.

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

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

Planet Pharma are partnered with a leading research organization to seek an experienced Laboratory Manager to oversee daily operations across busy, modern laboratories.

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

You will work with established clinical teams, researchers, research nurses, research practitioners and administrators to facilitate recruitment, sample collection, data entry and provide clinical support as required. You will liaise with the National Clinical Coordinator regarding appointments and

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

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 Nurses / AHPs / Clinical Research Practitioners support the delivery of clinical research across the Trust providing high quality patient care and data collection. Job Summary: Are you a Nurse, AHP or Clinical Research Practitioner who's passionate about improving patient care

Lead Clinical Research Associate, wakefield. Job Title: Lead Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research.