Clinical Research Co-Ordinator Jobs

73 jobs

Fixed term contract for 24 months This is an exciting opportunity for a Research Fellow (Trial Co-ordinator) to work on projects in the York Trials Unit (YTU). The York Trials Unit is a UKCRC registered clinical trials unit. You will be a member of the York Trials Unit under the direction of Professor David Torgerson within the Department of Health Sciences. The role will involve the following ...

Overview Henry Ford Health System, one of the largest and most comprehensive integrated U.S. health care systems, is a national leader in clinical care, research and education. The system includes the 1,100-member Henry Ford Medical Group, six hospitals, Health Alliance Plan (a health insurance and wellness company), Henry Ford Physician Network, a 150-site ambulatory network and many other healt...

Our Client is a world leader in Pharmaceuticals and Diagnostics. We are seeking a "Clinical Research Associate" for their clinical Operations Group to be based in Pleasanton, CA. Objectives of the Position To ensure timely implementation of clinical research plans for assigned products/projects To ensure investigator and site compliance with the study protocol, FDA regulations, ICH Guidelines a...

Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi...

Covance Clinical Research Unit, Inc. has an opening in Madison, Wisconsin, for a Senior Statistical Programmer (SAS Programmer III-Datasets). Provide input into assessments of resource requirements. Provide feedback to management to increase utilization, improve efficiency and amend the resource levels required on a project. Advise Senior Statistical Programming staff of changes in scope of proje...

Sr. Clinical Research Associate Requisition ID -2572692724 The Position Responsibilities Works under moderate guidance and participates in the planning and implementation clinical research projects;contributes technical and clinical operations expertise May co-ordinate the activities of relevant colleagues within the Company and investigators to ensure compliancewith the overall scientific s...

Objectives of the Position: To ensure timely implementation of clinical research plans for assigned products .To ensure investigator and site compliance with the study protocol, FDA regulations, ICH Guidelines and Good Clinical Practice GCP .To coordinate and execute clinical research activities for multisite clinical studies Scope Support the evaluation of RMS products Description of Responsibil...

Covance is currently recruting Clinical Research Associate/ Senior Clinical Research Associate in Sweden with oncology experience! Location: home based, Stockholm area About the job: • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and ...

Position : Clinical Research Assistant Location : Herzliya - Israel This is your chance to become part of a team that helps to bring miracle of medicine to market sooner. Covance is currently looking for a Clinical Research Assistant who will provide clinical support for projects : ° Act as contact for project team and study sites ° Perform CRF review, query generation and resolution agains...

Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. This is your chance to become part of a team that helps to bring miracles of medicine to market sooner. At the moment we are looking for: Clinical Research Assistants Responsibilities: Provide clinical support for projec...

Position : Clinical Research Associate (CRA) Division : Outsourcing Location : Israel - office-based or home-based You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Covance is one of the world's most dynamic drug development services companies CRO), providing integrated, tailored solutions to the pharmaceutical and biotechnolog...

Our client, a leading medical device company, is looking for a Sr Clinical Research Operations Manager with solid clinical research experience. Specifically, we are looking for someone who is able to handle the following responsibilities… 1) Co-ordinate department planning to ensure that the Clinical Operations Department functions optimally and within budget 2) Ensure that Clinical Operations D...

PURPOSE Provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications an...

Job Description Responsible to: Dr Paul Tiffin Responsible for: Delivery of a programme of quantitative research, predominantly in the field of medical education. This post is part-time (21 hours per week) and therefore the salary is pro rata. The post is fixed term until 28/02/2016. Job Summary and Purpose Undertake high quality, predominantly quantitative, research to inform educational polic...

OBJECTIVES: This position will report to the Head of Experimental Medicine in CNS TAU Clinical Science. This position will represent Clinical Development in the Global Project Team (GPT) and leads a matrix team in the GPT focused on Clinical Development in the early phases (Ph1-Ph2a POC). The position drives development of early clinical development plans (designing of FIH, Ph0, Ph1, Ph2 PoC st...

Description Responsible for conducting clinical studies to support Regulatory Affairs submissions and the Post Marketing Surveillance of Smith & Nephew ASD products, ensuring adherence to Good Clinical Practices (GCPs), SOPs, Smith & Nephew Code of Conduct and study protocols, in accordance with established budgets and timelines. ESSENTIAL FUNCTIONS Responsible for the day-to-day management of ...

Description Responsible for conducting clinical studies to support Regulatory Affairs submissions and the Post Marketing Surveillance of Smith & Nephew ASD products, ensuring adherence to Good Clinical Practices (GCPs), SOPs, Smith & Nephew Code of Conduct and study protocols, in accordance with established budgets and timelines. ESSENTIAL FUNCTIONS Responsible for the day-to-day management of ...

About Us We know that creativity doesn't happen on-demand. Developing cutting-edge cloud technology takes great minds and talented people working together in a collaborative environment. That is why we are committed to fostering an innovative, agile company culture; we encourage our teams to come together and experiment with new concepts, research new approaches and test out new technologies. On ...

About Us We know that creativity doesn't happen on-demand. Developing cutting-edge cloud technology takes great minds and talented people working together in a collaborative environment. That is why we are committed to fostering an innovative, agile company culture; we encourage our teams to come together and experiment with new concepts, research new approaches and test out new technologies. On ...

Remote Senior Scientist Patient Safety A leading pharmaceutical company in Gaithersburg, MD as an immediate need for a Patient Safety Scientist. Candidates can be remote or onsite. The general responsibilities for the Senior Pharmacovigilance Scientist are the same as for the Pharmacovigilance Scientist, although it is expected that given greater knowledge and experience such responsibilities may...