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The Role Are you looking for a new challenge? Do you want to work as part of a dynamic team that helps get new medicines to market? As a Clinical Research Technician, you will play a key role in providing a safe and caring environment for our volunteers who take part in our clinical trials. No prior clinical experience is required, a full training programme is provided. You can also enjoy free and secure on site parking. Key responsibilities of a Clinical Research Technician include: Collection ...Read more about Clinical Research Technician - Night shiftsMore
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The Role Responsible for the processing and registration of all screening volunteers, verifying proper identification and maintaining the participant directory. To comply & adhere to GCP guidelines and regulations as required of this role. To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards. To ensure subject safety at all times Main tasks and responsibilities Prepare and assemble screening charts. Register scre ...Read more about Registration CoordinatorMore
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The Role Supervise GMP Operations in the daily execution of Manufacturing processes, cleaning/sanitization procedures of the facility, equipment, and instruments. To comply & adhere to Good Manufacturing Practice (cGMP) standards. Main tasks and responsibilities will include: Support day to day operations with an “on the shop floor” presence. Monitor’s operators and equipment throughout shift to ensure all SOPs are properly followed and executed. Coaches’ operators on proper operation and ad ...Read more about Production SupervisorMore
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The Role Under the direction of the Team Leader, the incumbent is responsible for reviewing, updating, tracking and providing timely processing of all assigned documentation generated or executed within the clinical Manufacturing Department. As an Executed Batch Records (EBR) reviewer, this position is expected to conduct a full, comprehensive and complete EBR review on behalf of Clinical manufacturing group within 72 hours of batch documentation completion. EBRs consist of a stand-alone documen ...Read more about GMP Document ReviewerMore
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The Role Are you looking for a new challenge? Do you want to work as part of a dynamic team that helps get new medicines to market? As a Clinical Technician, you will play a key role in providing a safe and caring environment for our volunteers who take part in our clinical trials. No prior clinical experience is required, a full training programme is provided. Key responsibilities of a Clinical Technician include: Collection and recording of high-quality study data in compliance with the Study ...Read more about Clinical TechnicianMore
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The Role The QA Associate will support contract of clinical and commercial manufacturing for Pharmaceutical products during second shift. The QA Associate will support the technology transfer for clinical and commercial manufacturing and provide QA oversight of the manufacturing process during second shift. Ensure the implementation and maintenance of an efficient and effective quality management system, maintain open and timely communication across the teams, and visibly demonstrate the behav ...Read more about QA Associate (2nd Shift)More
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The Role The Research Volunteer Liaison (Activities Coordinator) works with the Clinical and Screening Teams to ensure the best possible experience for the volunteers, maximizing the potential for them to maintain compliance during their participation, to complete the trials and return for future studies Coordinates study volunteer activities (transportation to consultation or off-site procedure appointments) and addresses non-study related needs of volunteers during their inpatient stay a ...Read more about Activities CoordinatorMore
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The Role Responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications To comply & adhere to GCP guidelines and regulations as required of this role To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards To ensure subject safety at all times Main tasks and responsibilities Responsible for administering study medication to study participants Familiar with intravenous ...Read more about Clinical Research NurseMore
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Miami, FL, USA ● Req #5815 December 2023The Role Collects biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule. Tracks overall study event schedule and participant compliance. To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards. To ensure subject safety at all times Main Tasks and Responsibilities: Responsible for collection of biological samples; e.g. urine, and sputum. Responsible for drawing blood specimens (by v ...Read more about Clinical Research Technician (with Phlebotomy experience) - Full TimeMore
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Miami, FL, USA ● Req #5515 December 2023The Role Collects biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule. Tracks overall study event schedule and participant compliance. To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards. To ensure subject safety at all times Main Tasks and Responsibilities: Responsible for collection of biological samples; e.g. urine, and sputum. Responsible for drawing blood specimens (by v ...Read more about Clinical Research Technician (with Phlebotomy experience) Per DiemMore
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The Role This is a fantastic opportunity for a Registered Nurse looking to take the next step in their career in clinical research. You will work on a wide range of leading clinical trials with a multifunctional team, broadening your skills and helping pharmaceutical companies progress new medicines to market. The position will be clinic based at our Nottingham site and our facility is made up of 85 beds across 6 wards which has recently undergone extensive refurbishment and operates 24 hours a ...Read more about Clinical Research NurseMore
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The Role This is a fantastic opportunity for a Registered Nurse looking to take the next step in their career in clinical research. You will work on a wide range of leading clinical trials with a multifunctional team, broadening your skills and helping pharmaceutical companies progress new medicines to market. The position will be clinic based at our Nottingham site and our facility is made up of 85 beds across 6 wards which has recently undergone extensive refurbishment and operates 24 hours a ...Read more about Locum Clinical Research Nurse (Nights only)More
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Data Sciences at Quotient comprises over 100 staff and provides an expert service in the data management, pharmacokinetics, programming, statistical analysis and reporting of early Phase clinical studies. Due to our continued growth and success we have an excellent career opportunity for a talented Programmer to join our Statistical Programming department and further your career. You will be involved in the challenging environment of early phase clinical studies and play a key role in the expans ...Read more about Senior Statistical ProgrammerMore