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About the Company KPS Life is seeking a Clinical Study Associate Manager (CSAM) to support global clinical trials in partnership with the Clinical Study Lead, with responsibilities across study start-up, vendor/CRO oversight, site activation, and ongoing study execution. This is a great opportunity for a clinical operations professional with 4+ years of clinical research experience who wants to play a key role in delivering high-quality clinical trials from start-up through closeout. 3 days in the office Uxbridge is a must. About the Role The Clinical Study Associate Manager (CSAM) Service supports the Clinical Study Lead by taking responsibility for areas of clinical trial delivery. The Clinical Study Associate Manager works with the study team internally and externally with vendors such as CROs in feasibility, planning, initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and our Client’s Standard Operating Procedures (SOPs) and ICH/GCP. This Service applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) the balance of direct execution versus oversight of CROs deliverables will vary accordingly. Responsibilities • May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the study, • Contributes to risk assessment and helps identify risk mitigation strategies, • Supports feasibility assessment to select relevant regions and countries, • Oversees and provides input to the development of study specific documentation including but not limited to: case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc., • Reviews site level informed consents and other patient-facing study start-up materials, • Oversees setting up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and Trial Master File (TMF), • Contributes to investigator meeting preparation and execution, • Oversees engagement, contracting and management of required vendors for the study, • Oversees and provides input to study drug and clinical supplies forecasting, drug accountability and drug reconciliation, • Provides regular status reports to stakeholders as requested by the Clinical Study Lead, • Contributes to development of and oversees implementation of recruitment and retention strategies, • Monitors progress for site activation and monitoring visits, • Supports data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites, • Escalates data flow and data quality issues to Clinical Study Lead, • Oversees the execution of the specific clinical study deliverables against planned timelines, • Escalates issues related to timelines or budget to Clinical Study Lead, • Supports accurate budget management and scope changes, • Contributes to clinical project audit and inspection readiness throughout the study lifecycle, • Supports internal and external inspection activities and contributes to CAPAs as required, • Manages aspects of study close-out activities including but not limited to database lock, reconciliation of vendor contract, study budget, TMF and study drug accountability, • May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring Qualifications • Bachelor’s degree and minimum 4 years of relevant experience Required Skills • Technical proficiency in trial management systems and MS applications, including but not limited to Teams, MS Office, Project, CTMS, EDC, IWRS/IVRS., • Knowledge of ICH GCP and relevant regulatory guidelines/directives, • Demonstrated interpersonal & leadership skills, • Attention to details for the ability to deliver on specific study activities, • Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization, • Budget awareness with the ability to participate in various aspects of budget management, • Effective communication skills via verbal, written and presentation abilities Equal Opportunity Statement KPS Life is committed to diversity and inclusivity in the workplace.

A global biopharmaceutical services company is seeking a Clinical Research Associate II to join its team in the UK. This role provides a unique opportunity for clinical monitors to build relationships with sites, manage trials from start to finish, and ensure the quality of the research process.

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

The ideal candidate will have essential experience in oncology trials and RECIST criteria.

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). Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations

Parexel is seeking Clinical Research Associates, ideally with the oncology experience for upcoming openings. Responsible for all site management and monitoring activities across assigned oncology studies. Experience in, or willingness to monitor oncology clinical trials.

Job Title: Senior Clinical Research Associate. 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.

We are seeking an experienced Clinical Research Associate to join a dedicated single-sponsor team in England. Clinical Research Associate – England. As a CRA, you will be a key contributor to the successful delivery of clinical trials across England.

Job Title: Clinical Research Associate. 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, coordinating timely delivery and subsequent p

Previous experience as a Clinical Research Associate. Experience using clinical trial management systems.

Job Title: Principal Clinical Research Associate. Basic knowledge of drug therapy techniques and clinical research methodologies. Join a highly experienced team dedicated to excellence in clinical research.

Oversee and monitor clinical trials across multiple sites, therapeutic areas, and phases. Ensure adherence to clinical trial protocols, regulatory requirements, and industry standards such as GCP and ICH. CRA monitoring multi-centre clinical trials; experience in oncology or early-phase studies is a

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

Clinical Research Associate (FSP). At least 6 months of independent clinical monitoring. Contract Research Organization (CRO).

As a Senior Clinical Trial Associate, you are responsible for providing the administrative support to the clinical development/project teams and maintaining a range of clinical documentation. Proven track record in working within clinical research in the pharmaceutical, CRO or NHS environment. Catal

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

A full-service biotech CRO is seeking a Clinical Research Associate (CRA) to manage and oversee clinical studies in the United Kingdom. Ideal candidates have a degree in life sciences and at least 3 years of clinical trial experience, particularly in oncology or nephrology.

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK. IQVIA is a leading global provider of clinical research serv

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.

The post holder must have significant experience at NHS band 3, or equivalent, in a clinical setting, understanding and experience of the clinical research process, including ICH-GCP and research governance would be advantageous. The post holder must have significant experience at NHS band 3, or equ

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

A mid-sized Clinical Research Organisation is seeking a Clinical Research Associate (CRA) in West London. Join a supportive team dedicated to diverse clinical research projects. This role involves overseeing clinical trial sites across the UK and Ireland, ensuring compliance with regulatory standard

Senior/Lead Clinical Research Associate (CRA) - Remote in the United Kingdom. Get notified about new Clinical Research Associate jobs in. Significant independent monitoring experience within clinical research.

Senior Clinical Research Associate (Clinical Operations). Clinical Trial Associate, in‑house CRA, or similar clinical operations role. This role sits within a high‑performing clinical operations team supporting.

Experienced Clinical Research Associate page is loaded## Experienced Clinical Research Associatelocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted 9 Days Agojob requisition id: R1482675Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedic

Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies and clinical investigations: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. At least 3 years of experience

A leading Clinical Research Organization in the UK is looking for Clinical Research Associates. The role involves monitoring clinical trials, conducting visits, and ensuring adherence to protocols.

A global leader in clinical research services seeks Clinical Research Associates to monitor and manage clinical trials in Greater London.

Site-Based Senior Clinical Research Associate (CRA). This is a great opportunity for a motivated CRA to make a tangible impact in a dynamic clinical research environment. Manage day‑to‑day clinical trial activities at assigned sites.

At least 5 years’ experience as a Clinical Research Associate with proven track record managing clinical trial sites. Senior Clinical Research Associate (UK). Clinical Research Associate (Sr.

A leading global provider of clinical research services is seeking an Experienced Clinical Research Associate in Reading, UK. Candidates should have a life sciences degree and significant experience in clinical trial management.

Clinical Research Associate (or equivalent role). Clinical Research Associate (CRA). Clinical Research Associate (CRA).

A global clinical research organization in the United Kingdom is seeking a Clinical Research Associate to conduct on-site and remote monitoring visits. The role requires experience in clinical monitoring and knowledge of ICH-GCP and UK regulations.

A clinical research organization in England seeks a motivated CRA to oversee and monitor clinical trials across various sites.

Medpace is a full‑service clinical contract research organization (CRO) offering Phase I‑IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Entry Level - Clinical Research Associate. Our successful Clinical Research Associates come from varied b

Clinical Research Associate / Clinical Site Manager. We are seeking an experienced Clinical Research Associate (CRA) or Site Manager to manage and support the execution of clinical trials across multiple sites in Europe, including the UK, Spain, Italy, Germany, France, and Netherlands. Oversee the e

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate to oversee site management and ensure compliance with regulatory standards.

The Senior Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites. More than 5 years of experience as a Clinical Research Associate. Monitor assigned clinical trials and clinical sites by reviewing and reporting site enrollment, a