TRABAJO CLINICAL ASSOCIATE II SPONSOR

Join us in our exciting journey!! we currently require a motivated, passionate and enthusiastic clinical trials professional to join our rapidly growing clinical...

Senior clinical research associate iqvia is the human data science company oriented to drive human health outcomes forward... good clinical practice (gcp) and international...

Study start up associate ii - german speaker icon plc is a world-leading healthcare intelligence and clinical research organization... what you will be doing: leading...

Study start up associate ii - icf icon plc is a world-leading healthcare intelligence and clinical research organization... study start up associate (informed consent)...

Client services associate ii -spain/bulgaria/poland but will consider other eu locations - home or office based icon plc is a world-leading healthcare intelligence...

Req • knowledge of clinical trials - knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i...

clinical research associate iqvia spain is looking for talented and motivated team member to join our sponsor dedicated team as junior cra...

As a ssu associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence...

Escalate changes that fall outside the documented “fall-back” parameters, if available to the sponsor or to clinical site agreement manager as appropriate...

clinical study protocol (csp) through to clinical study report (csr)) in accordance with relevant az sops... experience in all phases of a clinical study lifecycle...

Arranges for the appropriate destruction of clinical supplies... 1-2 years of clinical trial monitoring experience is preferred... a minimum of 1 year of clinical...

Icon plc is a world-leading healthcare intelligence and clinical research organization... as a clinical research associate  you will be joining the world&rsquo...

In this highly specialized and dynamic cra role sponsor dedicated, you’ll utilise your extensive therapeutic knowledge in oncology to oversee uniquely-focused...

Partner with ww clinical operations to develop clinical strategies and ensure compliance with local, state, and federal regulations for conducting clinical trials...

Years of clinical trial monitoring experience is preferred... a minimum of 1 year of clinical trial monitoring experience is required...

Good clinical practice principles... you will develop specifications to ensure that statistical programming elements align with the overall deliverable and adhere...