Perceptive Informatics, a PAREXEL company, develops and offers a portfolio of sophisticated and innovative technology-based products and services that facilitate clinical drug development and are designed to decrease time to market for Biotech, Medical Device and Pharmaceutical Companies. We are offering an exciting opportunity for an experienced Proposal Developer to join a high performing team based in Nottingham. The scope of this...
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Date: 16 May
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Switzerland,
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Salary not specified
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2 applications
GMP Manager - CRO - Switzerland - Excellent salary and benefits Global provider of essential, pre-clinical and non-clinical contract research services to the pharmaceutical, biotech, medical device, agrochemical and chemical industries, as well as to academic and government and other research organizations seeks a GMP Manager to work in their facility in Basel-Country in Switzerland. Their focus is on providing customers with ...
The opportunity: This is an exciting opportunity to join the Project Management Department of Phlexglobal, an expanding, specialist provider of technology enabled document management solutions to the global clinical research market. The role: In this key role you will be managing the delivery of client facing projects and client relations to provide electronic Trial Master File (eTMF) and document solutions to our client...
A fantastic opportunity has arisen for an experienced Project Director/Manager within a leading CRO. Role: The role of Project Director is the key role that will be responsible for our clients’ projects and will be accountable for the delivery multiple projects to timelines and within budget. To make this role a success you will be required to work closely with multiple departments, whilst being able to demonstrate a...
Clinical Project Manager-Oxford-Permanent-CRO-£30K-£45k-Pharmaceutical-GMP This is an exciting opportunity for an experienced clinical project manager to join a fast growing biopharmaceutical company at a time when their lead product has entered Phase III and their follow-on products complete Phase II. The successful candidate will report to the CMC Development Manager. My client is seeking an office based Clin...
Exciting opportunity for a driven and highly motivated professional to develop the European business of a market-leading global central laboratory As Business Development Manager you will be selling central laboratory services into the pharmaceutical industry. You will apply your strong knowledge of clinical trial/central lab processes to promote appropriate service solutions to clients throughout the UK and EU. Based between...
Clinical Trial Patient Recruitment Project Manager Category: Pharmaceutical/Science & Research Type: Permanent Location: Southern UK Salary: £53,000+ Car and Benefits Do you have a strong background in clinical research with a good knowledge of drug development process? Have you worked in a project management capacity with budget management responsibilities? Do you have experience build...
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Date: 4 days ago
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Switzerland,
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Salary not specified
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0 applications
In this role you will: • Dictate cellular biomarker assays and strategy across a number of different projects spanning all phases of clinical trials • Lead strategic evaluation of cellular biomarkers required for the assigned clinical studies • Work in partnership with Translational Medicine and specific Disease Areas to drive the planning and execution of clinical studies You will bring to the role: • ...
Clinical Trial Medical Review Specialist Category: Pharmaceutical/Science & Research Type: Fixed Term Contract- Part Time 17.5 hours per week Location: Southern UK Salary: £35 per hour Do you have a strong background in clinical research with a good knowledge of drug development process? We’re working with one of the world’s best specialist pharma companies who are recruiting for a Clinica...
Due to continued expansion, we are working exclusively with a Cambridge based consultancy to recruit an experienced Consultant. Our client’s multinational team of postgraduate scientists, technologists and business strategists help companies explore product, process. You will have responsibility for end-to-end management of projects from client briefing, research design, primary (telephone) and secondary (literature) re...
Exciting opportunity for a seasoned Senior Director PAREXEL Consulting Key Accountabilities Responsible for a regional group within PC while being held accountable for successful business development and growth, execution of multiple projects and client satisfaction. A Senior Director has specific subject matter expertise supporting the development and delivery of PC services. Develops high growth ...
Job Description: Our client is looking for a Regulatory Compliance Administrator to be based in South West London. The company is involved in Phase I-IV research trials including pharmacokinetic studies in patients, and healthy volunteer studies. The Regulatory Compliance Administrator is responsible for assisting the Head of Regulatory Compliance and Regulatory Compliance Coordinator in all aspects of Regulator...
POST DOCTORAL HPC CLINICAL SCIENTIST Molecular Microbial Diagnostics My client is looking for a Post-doctoral HPC registered Clinical Scientist, with Molecular Microbial experience, to work within a busy specialist laboratory providing a clinically supported service for the rapid diagnosis and management of infectious and genetic disease. The appointee will work with our HPC-registered Clinical Scientists, where he...
9 jobs matching this search were posted in the last week
Job Description: We are assisting our client in recruiting a Senior Clinical Research Associate. This is a permanent position office based in Cambridgeshire. Under limited supervision, the Senior CRA monitors and oversees clinical practices for one or more multi-site clinical trials, ensuring compliance with all regulatory agency requirements. Maintains sound clinical practices to ensure validity of study. Monitors the cond...
Job Description: We are assisting our client in finding a Senior Specialist for their Phase I unit in North West London. The post holder will provide guidance on requirements for the conduct of clinical trials including: • Maintain drug accountability records in accordance with agreed protocols and the principles of International Conference on Harmonization Good Clinical Practice (GCP) and Good Manufacturing Practice (...
Job Description: Our client is a fast growing CRO who are seeking an experienced Proposals and Contracts Manager for their Horsham office. Core Accountabilities: • Prepare contracts, proposals and contract amendments. Responsibilities include proposal and change order preparation, payments schedule generation and cash flow analysis, task orders creation, internal budget and client grid completion. • Provide ...
Job Description: Our client is a fast growing CRO seeking and Associate Director of Project Management to manage Project Managers and assist them in the execution of projects to a high standard of quality and within contractual budget and timelines. The successful applicant will work across departments and locations to ensure PMs are delivering a quality full-service product to the sponsors and to oversee/ensure all aspects...
Job Description: With the growth of their market access and healthcare value demonstration activities our client, a leading Market Access, Health Economics and Outcomes research consultancy, wishes to appoint an ambitious (senior) Research Associate with a genuine passion for understanding and communicating the science of healthcare value. The role will involve contributing to international projects by performing both quali...
Job Description: Our client, a leading Market Access, Health Economics and Outcomes research consultancy, is looking to recruit a highly motivated Research Associate in their Endpoint Development & Outcomes Assessment team, who is looking to apply and enhance their healthcare research skills in a challenging and rapid-moving field. This is an exciting and varied role in which you will be involved in studies focused on ...
Job Description: Our client, a leading Market Access, Health Economics and Outcomes research consultancy, wishes to appoint an ambitious Manager-level consultant with a genuine passion for understanding and communicating the science of healthcare value. Our clients purpose is to improve patients’ lives by informing healthcare decisions. To do this we help our clients bring healthcare products and services to the market succe...
Job Description: Our client, a leading Market Access, Health Economics and Outcomes research consultancy, is looking to recruit a highly motivated Health Economist / Senior Health Economist. Our clients purpose is to improve patients’ lives by informing healthcare decisions. To do this we help our clients bring healthcare products and services to the market successfully by investigating, developing and communicating scientif...
Job Description: Our client, a leading Market Access, Health Economics and Outcomes research consultancy, is looking to recruit a highly motivated Market Access Director or Associate Director to their Value Insight & Communication practice. This is an exciting leadership role in which you will provide scientific and strategic input to various types of market access projects. Whilst supporting the growth and development ...
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Date: 2 May
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France,
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Competitive salary
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0 applications
Job Description: Our client is a global CRO who are seeking a Medical Director in their Paris office. This role is an essential function within the Global Medical Department responsible for medical monitoring of assigned projects and providing expertise on all medical related aspects within the field of Pulmonology. Main Accountabilities: - Medical monitoring - answering day to day medical and scientif...
Job Description: Our client is a globally recognised top CRO who are looking for a Senior Clinical Monitoring Associate to be based in West London. The responsibility of a Senior Clinical Monitoring Associate is to independently perform and organize remote clinical monitoring tasks and visits for designated projects in accordance with relevant SOPs and regulations. Responsible for coordinating a moderate to large ...
We are assisting our client, a medical communications agency, in finding a (senior) medical writer to be based in Cheshire or London. There will be a full & varied workload, including publications-related work, meetings (advisory boards, symposia, masterclasses), multi-media deliverables, etc. Key objectives • To consistently produce high quality medical education & communications materials for the pharmaceutic...
