01.01.2012 | Pełny etat | Warszawa | Hays PolandOur client, prestigious Clinical Research Organisation is currently seeking Clinical Project Manager to join their Warsaw successful candidate will coordinate and manage the activities of the studies, costs and project team to agreed timelines adhering to SOP’s and ICH-GCP. Your
Zobacz później01.01.2012 | Pełny etat | | Stany Zjednoczone | Wielka Brytania | Hays PolandActivities. The new teaching hospital and state-of-the-art health care facilities have attracted a great deal of attention, locally nationally and internationally. Delegations from around the globe have come to study how to design and run a modern and flexible hospital. The Hospital was named one
Zobacz później01.01.2012 | Pełny etat | Małopolskie | Hays PolandAccording to Standard Operating Procedures and GCP Guidelines Experience - Skills Required · Minimum of 3 years of clinical research monitoring experience · Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP. · Experience in cardiology essential · Good
Zobacz później01.01.2012 | Pełny etat | Mazowieckie | Hays PolandClinical Project Manager An international CRO with offices in Warsaw is currently looking for Clinical Project Manager /Senior Clinical Project Manager to join their team. Role Responsibility You will coordinate and manage the activities of the studies, costs and project team to agreed timelines
Zobacz później01.01.2012 | Pełny etat | | | Hays PolandOf Responsibilities - Debug, and design and implement software solutions in our new and present equipment, - Conduct pre-studies (experiments, measurements) to verify ideas and adjust the software if necessary, - Work closely with the customer getting their requirements and study the feasibility, - Requires to work
Zobacz później01.01.2012 | Pełny etat | Mazowieckie | Hays PolandIs responsible for the course of the clinical trial in adherence to the SOPs under consideration of the project-specific guidelines and the company directives. Core Activities • Self-study of study-specific documents and responsible for reporting of incomplete background to the project leaders (CPM
Zobacz później01.01.2012 | Pełny etat | Mazowieckie | Hays PolandOf Job Specification Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines in two therapeutic areas - oncology and cardiology Job Duties and Responsibilities - Responsible for all aspects of study site monitoring including routine
Zobacz później01.01.2012 | Pełny etat | Hays PolandOraz rekrutacja badaczy - wypełnianie odpowiedniej dokumentacji o statusie badania (study status report) - dostarczenie na czas odpowiedniej dokumentacji do komisji etycznej (protocol/consent documents/safety reports)
Zobacz później01.01.2012 | Pełny etat | Hays PolandOur clienta niche oncology CRO, is currently searching for Senior CRA in Poland. Our client has an excellent reputation for client service and has grown through recommendations from existing sponsors and study sites, as well as repeat business from satisfied clients
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