Site supervisor Jobs in Großpösna
Jobalert für diese Suche erstellen
Site supervisor • großposna
- Gesponsert
Clinical Trial Manager - Dach region - oncology
PharmiwebLeipzig, DEReinigungskraft (m / w / d)
RAHMER DienstleistungenLeipzig, DE- Gesponsert
Leitung eines Blutspendezentrums
Haema Blut- und PlasmaspendedienstLeipzig, DE- Gesponsert
Supervisor / Teamleiter (m / w / d)
Future Electronics EDC Services GmbHLeipzig, GermanySupervisor / Nachwuchsführungskraft im Verkauf (m / w / d)
JD SportsLeipzig, Sachsen, DeutschlandHead of Waste Treatment (m / f / d)
GULP – experts unitedLeipzigSupervisor / Nachwuchsführungskraft im Verkauf (m / w / d)
JD GroupLeipzig- Gesponsert
Oberarzt Psychiatrie und Psychotherapie w / m / d (28461)
Doc PersonalBeratung GmbHLeipzig, Sachsen, GermanyGerman Social Media Content Analyst in Lisbon w / Relocation bonus
Cross Border TalentsLeipzig, GermanyWind and Site Engineer
The Green Recruitment CompanyLeipzigManager Site Assessment / Standortbewertung Wind & Site (m / w / d)
Juwi GroupBrandisSupervisor (m / w / d) Mobile Sicherheitsdienste
Securitas DeutschlandLeipzig, Saxony, Germany- Gesponsert
PXT Snr Specialist Op Excellence, DAN PMO - Operational Excellence
Amazon Europe CoreLeipzigSite Controller (w / m / d)
Straumann GroupLeipzig, Germany- Gesponsert
Junior DevOps- / Site Reliability Engineer (m / w / d) - System Engineering / Admin, Ingenieur
IT Sonix Custom DevelopmentLeipzig, DEService Schichtleiter | Supervisor Frühstück (m / w / d)
H4 Hotel LeipzigLeipzigSenior Projektmanager / Site Manager Construction Management Hochbau- und Industriebau (w / m / d)
ArcadisLeipzig, Sachsen, GermanyClinical Research Nurse I
Thermo Fisher ScientificLeipzig, GermanySupervisor (m / w / d) Service Controlling AurumTours
CHECK24 VergleichsportalLeipzigCampus Internship - Logistics : Optimization & Digitalization
DOW OLEFINVERBUND GMBHBoehlenClinical Trial Manager - Dach region - oncology
PharmiwebLeipzig, DEAs a Clinical Trial Manager you will be leading the Local Study Team(s) (LSTs) at country
level to deliver committed components of clinical studies according to agreed resources, budget and
timelines complying with Procedural Documents and international guidelines such as ICH-GCP
as well as relevant local regulations.
In addition to leading LST(s), as the CTM you may perform site
monitoring as needed to support the flexible capacity model.
Key responsibilities
- Has the overall responsibility for the study commitments within the country and for
timely delivery of data to required quality.
assigned study / studies
ensuring compliance with SOPs, ICH-GCP and local regulations.
studies is performed to the highest quality.
performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits
to evaluate suitability and quality risks.
and maintains accurate study budget in the clinical studies financial system by regular
checks of the system and financial reports