In-house Clinical Research Associate II – EMEA – Home based
... very heart of every successful clinical trial. Working alongside brilliant minds across ...
... very heart of every successful clinical trial. Working alongside brilliant minds across ...
... very heart of every successful clinical trial. Working alongside brilliant minds across ...
... timelines IT proficiency: MS Office, clinical trials systems (e.g. IMPACT, IWRS, ... Poland is responsible for conducting clinical trials across this group of countries, providing clinical trial management and administration support to ...
... understanding and working knowledge of clinical research, phases of clinical trials, current GCP ICH & country clinical research law & guidelines. Excellent understanding ... and training programs related to clinical trials, therapeutic areas, hard and soft ...
... working with the physicians within Clinical Development to provide clinical research support for programs as ... at least 5 years as clinical research scientist in oncology are ... ,000 Sites and 675,000+ Trial patients. No matter what your ...
... timelines IT proficiency: MS Office, clinical trials systems (e.g. IMPACT, IWRS, ... global patients in Novo Nordisk clinical trials. Working at Novo Nordisk Novo ...
... review and proficient revisions of Clinical Trial Agreements with focus on liability ... , and negotiating confidentiality and clinical trial agreements with CROs and study sponsors · Experience working in a clinical trial setting to include, CRO, site ...
... , oversee the conduct of the trial through all phases, work on ... 17 years ago as a Clinical Operations Assistant. Through the years, I followed a Clinical Operations development path and now I am a Senior COL. Parexel provides many career ...
... meetthe most challenging needs facing clinical trials today.We’re looking for a Clinical Lead II III –Oncology to join our Clinical Management teamthat is passionate about ...
... review and proficient revisions of Clinical Trial Agreements with focus on liability ... , and negotiating confidentiality and clinical trial agreements with CROs and study sponsors · Experience working in a clinical trial setting to include, CRO, site ...