TRABAJO CLINICAL ASSOCIATE LEVEL II

Abiomed, part of johnson & johnson's medtech, is recruiting for a clinical research associate ii... our team focuses on future development of the impella platform...

The position will involve conducting mechanistic pbpk using clinical data to support the clinical development of drug candidates across therapy areas...

The associate director study leader, early oncology clinical is responsible for the delivery of clinical studies including quality, timelines, budgets, resources...

May oversee overall quality of the clinical database... precision for medicine is seeking an experienced senior clinical data associate to provide comprehensive...

Arranges for the appropriate destruction of clinical supplies... a minimum of 2 years of clinical trial monitoring experience is required...

Arranges for the appropriate destruction of clinical supplies... tracks costs at site level and ensure payments are made, if applicable... responsible for the implementation...

포지션: clinical research associate 계열사: 얀센 (janssen) 근무지: 서울시 용산구 근무 형태: regular [summary] a clinical research associate (site manager i (sm i)) serves as the primary...

Ability to lead and motivate a clinical team also required... join iqvia on our mission to drive healthcare forward! we are recruiting for a clinical fsp associate...

Depending on the program scope, the ctm ii may have study level responsibilities similar to any other ctm... assisting the cpl by tracking compliance to all study...

The senior site manager will collaborate with the local trial manager (ltm), clinical trial assistant (cta), and clinical trial manager (ctm) to ensure overall site...

Study start up associate ii as a member of the study start up team, you will play an integral role in making sure that physicians at our research sites are prepared...

Icon plc is a world-leading healthcare intelligence and clinical research organisation... the role: • to review and negotiate clinical site investigator contracts...

€¢ *to acquire knowledge of ich gcp, the conduct of clinical trials and governing regulations, relevant icon sops, icon internal tracking systems and client sops...

The qa associate ii is responsible for providing quality assurance and quality oversight services to designated manufacturing sites... the associate ensures compliance...

• proactively collaborates with the site & study operations (sso) clinical project managers (cpm) and cra managers as well as medical science liaisons, clinical...

clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...

Facilitate communication between clinical sites and other abbott clinical staff (e... maintain and develop a productive clinical territory: develop and maintain...

Experience particularly in phase ii and phase iii clinical development... understanding of scientific and clinical issues related to the design and implementation...