At least 3 years of experience as a Clinical Research Associate Clinical Monitor. Excellent knowledge of.. Good knowledge of all functional areas of clinical trial management. Working knowledge of current ICH..
When our values align, there's no limit to what we can achieve. Parexel FSP is currently seeking Senior Clinical Research Associates and CRAII in any home based location in Poland.As a top..
Raises observed deficiencies and issues to clinical management expeditiously and follow all issues.. Integrity, Intensity, Innovation and Involvement. working together to accelerate research, solve complex..
If you want to. Join a multi award winning leading biopharmaceutical company Be part of growing team of Clinical Research Associates Use new technology and smart monitoring tools Have..
The position As Clinical Research Associate your role is to verify the accuracy and completeness of the.. MS Office, clinical trials systems (e.g. IMPACT, IWRS, ePRO, InForm) On a personal level, you should..
Job DescriptionAs a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic..
CRASDAJD. CRA. SCRA. SeniorCRA. iqviaIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in..
Are you a dedicated clinical trial professional with solid site management experience? Are you highly.. this role might be just for you! The position As Clinical Research Associate your role is to verify the..
We also have a Research Center of Excellence in New Haven, Connecticut, global supply chain and.. In this context, we are looking the Clinical Research Associate (CRA), who has local responsibility for..
We are a leading global mid size Contract Research Organization (CRO) that partners with biotechnology.. TFS HealthScience is looking for a Senior. Clinical Research Associate to be home based in Poland..
Job Description As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic..
JOIN OUR TEAM! As of now we are looking for a Krakow based or home based (PL) Clinical Research Associate (m f d) full time. Tasks You will be tasked with the day to day Clinical Trial..
Job Title. Clinical Research PhysicianLocation. On site in Gdynia, PolandSalary. Up to 270,000PLN.. Global CRORoleIn this position you will conduct all clinical trials (studies) according to ICH GCP..
Are you an outstanding team player, passionate about delivering impeccable quality? Then join us as our new. Associate Risk Research Analyst!What you will do Conduct time efficient full analysis..
Requisition Number7581Employment Type RegularWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and..
Requirements Previous experience in a CTA, trial coordinator, or research nurse role would be.. Proficiency in relevant clinical research regulatory requirements, including GCP and UK statutory..
Description Position at Premier Research At Premier Research, we help biotech and specialty pharma.. We're looking for a Clinical Lead II III. Oncology to join our Clinical Management team that is..
More senior members of the associate team may mentor junior associatesAssociates with experience in.. with minimum of 2 years of experience in clinical operations (Senior Associate).Bachelor's degree (or..
Precision for Medicine is seeking an experienced Senior Clinical Data Associate to provide comprehensive.. Candidates should have Data Management experience working for a Clinical Research OrganisationBachelors..
Everest Clinical Research ( Everest ) is a full service contract research organization (CRO) providing a.. Assume a leader mentorship role in the training of safety associates for PV and drug safety activities..
Description , as this will not be available post closure of the advert. When applying for this role, please use the. cover letter' of the online application or your CV to describe ..
Overview Medpace is a full service clinical contract research organization (CRO). We provide Phase I IV clinical development services to the biotechnology, pharmaceutical and medical device..
The Associate Project Manager ensures the successful initiation, planning, execution, monitoring.. IDEAL PROFILE. Education. B.Sc. in a related field of study to clinical research Experience. Minimum 5..
Able to predict the result of action in advance and evaluate options to achieve goals.Who you are At least 10 12 years in clinical research in a CRO or Pharmaceutical Biotechnology Industry..
Responsibilities Assisting portfolio managers in daily routine duties Developing investment process using quantitative tools Building reports, market data analysis Preparing materi..
W związku ze stałym rozwojem firmy, poszukujemy osoby na stanowisko Senior Clinical Budgets Associate.OczekiwaniaPierwsze doświadczenie w obszarze badań klinicznych, bądź w podobnym..