Posts Tagged ‘Safety’
Drug Safety Associate / Senior Drug Safety Associate – Germany
September 1st, 2010 | 
Author: Our client, a leading global CRO, provides a comprehensive range of services in Phase I-IV clinical trials to the biopharmaceutical and device industries. They are currently seeking a Drug Safety Associate / Senior Drug Associate for their offices near Frankfurt.
JOB ROLE:
The Drug Safety Associate / Senior Drug Associate will be responsible for monitoring and tracking Serious Adverse Events, serious and non serious drug adverse reactions and other medically related project informatio…
Galapagos is looking for a QUALITY and SAFETY MANAGER in Drug Discovery – Mechelen, Belgium. The Quality and Safety Manager is responsible to ensure that Galapagos’ Drug Discovery activities at the Mechelen, Romainville and Leiden sites are quality driven and operating in a safe working environment.
The Quality and Safety Manager is responsible to ensure that Galapagos’ Drug Discovery activities at the Mechelen, Romainville and Leiden sites are quality driven and operating in a safe working environment.
Promotes quality achievement and performance improvement throughout the…
Posted in Scholarships | 
Tags: activities, Belgium, discovery, driven, Drug, ensure, environment, Galapagos, Galapagos’, Leiden, looking, Manager, Mechelen, Operating, Quality, responsible, Romainville, safe, Safety, sites, working | 
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Physician, Scientist or Consumer Safety Officer – Bethesda and/or Rockville, Maryland
Do you have a passion for cutting-edge
science and protecting the public health?
Unleash your passion into a rewarding career as a Physician, Scientist or Consumer Safety Officer at the Center for Biologics Evaluation and Research!
The Center for Biologics Evaluation and Research’s mission is to protect and enhance the public health through the regulation of biological products including blood, vaccines, allergenics, tissues, and cellular and gene therapies. Biologics, in contrast to drugs that are chemically synthesized, are derived from living sources (such as human, animals, and microorganisms) and are not easily identified or characterized, and many are manufactured using biotechnology. These products often represent cutting-edge biomedical research and, in time, may offer the most effective means to treat a variety of medical illnesses and conditions that presently have few or no other treatment options.
For details on qualifications and salary, please visit our Hiring Opportunities page at http://www.fda.gov/AboutFDA/CentersOffices/CBER/ucm125465.htm.
How to Apply:
For current vacancies and application procedures, visit: http://www.fda.gov/AboutFDA/CentersOffices/CBER/ucm103202.htm.
For future vacancies, submit CV/resume & cover letter to our resume bank to: CBER.Employment@fda.hhs.gov
Attn: Job Code: NS/Gen
The Center for Biologics Evaluation and Research is part of the Food and Drug Administration, Department of Health and Human Services.
EQUAL OPPORTUNITY EMPLOYER. SMOKE FREE ENVIRONMENT.
America’s Veteran: http://www.fedshirevets.gov/
Health and Safety Executive – Maternity Cover
Health and Safety Executive – Maternity Cover – 12-14 months
A leading global Pharmaceutical Research and development organisation, our client employs over 100,000 and
A leading global Pharmaceutical Research and development organisation, my client employs over 100,000 people worldwide and discovers, develops and successfully markets innovative products to prevent and cure diseases, to ease suffering and to enhance the quality of life.
An opportunity has arisen for an experienced Health and Safety Executive in their prestigious site in West Sussex to cover a maternity leave.
The candidate will work as part of a small team, have a degree in life science and hold the NEBOSH certificate. If you have worked in a biological or chemical environment, this would be an added advantage, although lab based experience is also very valuable.
Excellent communication skills and a flexible attitude are also qualities my client is looking for.
In return, my client can offer exceptional working conditions, with free on site parking, subsidised deli and restaurant and use of the on site gym.
Key Words
NEBOSH
Biology
Chemistry
Laboratory
Junior Teacher in Pharmacoepidemiology and Drug Safety (0,8 fte)
The teacher will be responsible for the development of e-Learning modules, participation in e-Learning modules, coordination of WP7, and accreditation of the master programme at Utrecht University. This position is available within the Eu2P project (http://www.eu2p.org). Eu2P (European Programme in Pharmacovigilance and Pharmacoepidemiology) is a collaborative European project that aims to develop a European Master programme in Pharmacoepidemiology & Pharmacovigilance that will be mainly based on e-Learning principles. Eu2P is designed to enhance understanding and communication on the benefit and risk of medicines and overall improve the citizen health protection. The University of Bordeaux and Roche are the coordinators of Eu2P. They manage a multi-national consortium including academics, regulators, and EFPIA companies. The division of Pharmacoepidemiology & Pharmacotherapy leads work package 7 that is aimed at developing several e-Learning modules in the area of Benefit-Risk assessment.
Drug Safety Assistant
Our client, known as the world’s premier research-based pharmaceutical company, discovers, develops, manufactures and markets a wide range of innovative, value-added pharmaceutical products for both humans and animals around the world. They are currently seeking a Drug Safety Assistant to join their offices based in the South East of England on a 4 month contract role.
JOB ROLE: The Drug Safety Assistant will assist in the input and processing of adverse event data generated from spontan…
Senior Drug Safety Executive
Senior Drug Safety Executive – - Great senior role for PSUR writer – 45,000 Nonstop is working closely with an interesting organisation in recruiting a Pharmacovigilance Scientist. The company will provide you with very strong experience and have one of the best training programs in the industry. You will be given the opportunity to utilise your experience and aid the company by working with some of the biggest names in the industry. As Pharmacovigilance Scientist, some of responsibiliti…
Drug Safety Associate / Senior Drug Safety Associate
Our client, a leading global CRO, provides a comprehensive range of services in Phase I-IV clinical
trials to the biopharmaceutical and device industries. They are currently seeking a Drug Safety Associate (all levels) for their Medical Safety Department in the UK South.
JOB ROLE:
In your role as Drug Safety Associate you will be responsible for monitoring and tracking Serious Adverse Events, serious and non serious drug adverse reactions and other medically related project informati…
Project Manager in Pharmacoepidemiology and drug safety (0,8 fte)
This position is available within the PROTECT-EU project (http://www.imi-protect.eu) . PROTECT-EU (Pharmacoepidemiological Research on Outcomes of Therapeutics by a European Consortium) is a collaborative European project that comprises a programme to address limitations of current methods in the field of pharmacoepidemiology and pharmacovigilance. The overall goal of PROTECT is to strengthen the monitoring of benefit-risk of medicines in Europe. The European Medicines Agency (EMA) is the coordinator of PROTECT and GSK is the deputy co-ordinator of PROTECT. They manage a multi-national consortium of 29 partners including academics, regulators, SMEs and EFPIA companies.
The division of Pharmacoepidemiology & Pharmacotherapy leads work package 2 that is aimed at developing, testing, and disseminating methodological standards for the design, conduct and analysis of pharmacoepidemiological studies.
Under the supervision of the principal investigator, the project manager will be responsible for the management of work package 2 of PROTECT, in which 18 public and private partners participate. Depending on the profile of the candidate, participation in the research is possible.
3 PhD researcher in Pharmacoepidemiology and drug safety
All positions are available within the PROTECT-EU project (http://www.imi-protect.eu) . PROTECT-EU (Pharmacoepidemiological Research on Outcomes of Therapeutics by a European Consortium) is a collaborative European project that comprises a programme to address limitations of current methods in the field of pharmacoepidemiology and pharmacovigilance. The overall goal of PROTECT is to strengthen the monitoring of benefit-risk of medicines in Europe. The European Medicines Agency (EMA) is the coordinator of PROTECT and GSK is the deputy co-ordinator of PROTECT. They manage a multi-national consortium of 29 partners including academics, regulators, SMEs and EFPIA companies.
The division of Pharmacoepidemiology & Pharmacotherapy leads work package 2 that is aimed at developing, testing, and disseminating methodological standards for the design, conduct and analysis of pharmacoepidemiological studies. The results of the PhD’s work will be presented at international scientific meetings, and will be published in peer-reviewed scientific journals. The PhD work should lead to a dissertation and a PhD degree.
PhD project 1: This project aims to evaluate and improve innovative methods to adjust for observed confounding. The project will use simulated data and real data from large health care databases and focus on propensity scores.
PhD project 2: This project aims to evaluate and improve innovative methods to adjust for unobserved confounding. The project will use simulated data and real data from large health care databases and focus on instrumental variables and various sensitivity analysis methods.
PhD project 3: This project aims to evaluate the influence of methodological parameters on associations between drugs and adverse events in different EU health care databases and disease registries.