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Broad understanding of clinical research principles and process. Join us! At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at

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 SENIOR CLINICAL RESEARCH ASSOCIATE OPPORTUNITIES. Parexel are currently registeri

A global clinical research organization is seeking a Clinical Research Associate to conduct site visits, review safety information, and ensure regulatory compliance. You will play an integral part in advancing clinical research across various therapeutic areas while receiving support for your profes

This position offers an exciting opportunity for clinical research professionals looking for a new challenge. A major NHS Trust in the United Kingdom is seeking a highly motivated Quality Assurance Manager to oversee the quality of clinical research. Ideal candidates will have proven research experi

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

A leading healthcare provider in Wales seeks a Research Nurse for a fixed-term position. The role involves supporting research participants, ensuring compliance with protocols, and working collaboratively within a team. Candidates should be Registered Nurses with a strong attention to detail and an

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

In this pivotal role, you will guide research teams and ensure high-quality clinical research for non-interventional studies on a global scale. A global healthcare organization in the United Kingdom is seeking a Senior Lead Clinical Research Associate (CRA). This position offers the opportunity to m

Clinical Research Associate II, this position will be fully home based working in the UK. 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 regulation

A leading pharmaceutical company is seeking a Senior Clinical Research Physician to provide leadership in global clinical studies focusing on non-obstructive respiratory diseases. Responsibilities include driving clinical trial designs, ensuring data integrity, and communicating results.

A global pharmaceutical leader is seeking a Senior Clinical Research Physician to provide strategic leadership for clinical studies focused on non-obstructive respiratory diseases. The ideal candidate should have a Medical Doctor degree, at least 5 years of experience in the pharmaceutical industry

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. Ideally, you will have some initial experience in the statistical analysis of clinical studies.

Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs. Senior Clinical Research Associate. Be part of a mission-driven organisation dedicated to advancing clinical research and transforming lives.

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 - 10 years) in the statistical evaluation of clinical trials in a CRO or the pharmaceutical indust

A leading pharmaceutical company is seeking a Medical Monitor to oversee clinical trial safety and compliance.

A clinical research organization in the UK seeks a detail-oriented professional for clinical document management, including the creation and proofreading of regulatory documents.

Proven experience in the pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research programs and registration activities, preferably for vaccines, or;* An investigator with significant experience in vaccine clinical studies in academic, NGO or

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

Responsibilities include recruitment, clinical assessments, and managing research projects on psychotic disorders. A leading academic institution in the UK seeks a Researcher to join the Department of Psychosis Studies.

A leading CRO in the UK is seeking a Clinical Research Associate (CRA) who will monitor clinical studies and ensure compliance with all standards.

Part of this service includes a NHS research delivery team consisting of Research Nurses, Clinical Studies Officers, Research Officers and Administrators, employed by NHS organisations to support the delivery of high quality health and social care studies. Part of this service includes a NHS researc

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.

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 prominent health organization in Wales is seeking a Research Nurse to ensure participant well-being during research activities. Candidates should be registered nurses with knowledge of research responsibilities and appreciated skills in data analysis. The role involves supporting research processe

Proven experience in the pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research programs and registration activities, preferably for vaccines, or;* An investigator with significant experience in vaccine clinical studies in academic, NGO or

Contractor Senior Clinical Research Associate CNS/Oncology- UK - Remote page is loaded## Contractor Senior Clinical Research Associate CNS/Oncology- UK - Remotelocations: England, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: JR101745Who we areWe’re a glo

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

We are hiring a Clinical Research Associate II, this position will be fully home based working in the UK. 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 appli

The role involves conducting original research, maintaining clinical competencies, and contributing to neurology clinics. A leading UK university is seeking a PhD Fellow to research neurodegenerative disorders. Candidates should have prior research experience and be GMC registered or qualified.

A clinical research services firm in the United Kingdom is seeking a Project Manager for biostatistical services. The ideal candidate will have a degree in statistics or related fields, along with 5-10 years of experience in the statistical evaluation of clinical trials.

Drive medical and scientific input into clinical trial design and execution in accordance with the Clinical Development Plan and related key clinical documentation (e. Enhances clinical study execution, working cross-functionally with internal stakeholders and the Clinical team to uphold medical and

Proven experience in the pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research programs and registration activities, preferably for vaccines, or;* An investigator with significant experience in vaccine clinical studies in academic, NGO or

It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D project and po

Oracle Life Sciences empowers pharmaceutical, biotechnology, medical device companies, and clinical research organizations to bring therapies to market faster and more efficiently. Senior Lead Clinical Research Associate (CRA) to drive success as part of our Non-interventional Study team.

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.

Organisation/Company KINGS COLLEGE LONDON Research Field Literature Researcher Profile Recognised Researcher (R2) Established Researcher (R3) Country United Kingdom Application Deadline 4 Jan 2026 - 00:00 (UTC) Type of Contract Other Job Status Full-time Is the job funded through the EU Research Fra

A leading clinical research organization in the United Kingdom is seeking a Senior Clinical Research Associate to oversee clinical monitoring and site management. The ideal candidate will have 5–7+ years of experience in clinical research, excellent organizational skills, and a Bachelor's degree i

Your expertise will help us navigate the complexities of clinical research as we strive to deliver meaningful solutions to healthcare challenges. At Rho, we believe in the power of passionate individuals working together to make a difference in clinical research. As a Clinical Research Associate II

At Rho, we believe in the power of passionate individuals working together to make a difference in clinical research. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity

Clinical Research Associate (French/German Speaking) (Remote) page is loaded## Clinical Research Associate (French/German Speaking) (Remote)locations: United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: REQ-2025-13114Job Title: Clinical Research Associate (French/Ger

A leading clinical research organization in the UK is seeking a Senior Clinical Research Associate who will ensure data integrity and compliance with regulatory standards.

Clinical research expertise: At least 3 years of experience as a CRA, including site initiation, Trial Master File (TMF) management, and site monitoring for both clinical and non-interventional studies. Train and coordinate CRAs: Oversee, mentor, and train a cross-country team of Clinical Research A

A major biopharmaceutical company in the United Kingdom is seeking a Clinical Medical Monitor to ensure patient safety and compliance during clinical trials.

A clinical research company in the United Kingdom is looking for a professional to engage in statistical analysis plans and validate statistical evaluations of clinical studies using SAS.

Proven experience in the pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research programs and registration activities, preferably for vaccines, or;* An investigator with significant experience in vaccine clinical studies in academic, NGO or

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 conduct all other programming activities needed during a clinical study. You have professional e

A clinical research company is seeking an experienced Senior Statistical Programmer to join their remote team in the UK. The role involves programming, validation, and quality control of statistical analyses for clinical studies using SAS.

A global pharmaceutical company seeks a Medical Monitor to oversee clinical trial safety and provide critical medical advice to study teams. The role involves monitoring safety issues, ensuring compliance with regulatory standards, and contributing to the development of clinical documents.