Site supervisor Jobs in Borsdorf
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Site supervisor • borsdorf
- Gesponsert
Clinical Trial Manager - Dach region - oncology
PharmiwebLeipzig, DE- Gesponsert
Supervisor / Teamleiter (m / w / d)
Future Electronics EDC Services GmbHLeipzig, Sachsen, Germany- Gesponsert
Oberarzt Psychiatrie und Psychotherapie w / m / d (28461)
Doc PersonalBeratung GmbHLeipzig, DETechnischer Sachbearbeiter Ersatzteile (m / w / d)
FläktGroup Deutschland GmbHWurzen, Sachsen, DeutschlandSupervisor / Nachwuchsführungskraft im Verkauf (m / w / d)
JD SportsLeipzig, Sachsen, DeutschlandHead of Waste Treatment (m / f / d)
GULP – experts unitedLeipzigWind 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 CoreLeipzigSupervisor / Nachwuchsführungskraft im Verkauf (m / w / d)
JD GroupLeipzigReinigungskraft im Hotel (m / w / d)
RAHMER DienstleistungenLeipzig, DEGerman Social Media Content Analyst in Lisbon w / Relocation bonus
Cross Border TalentsLeipzig, Germany- Gesponsert
Junior DevOps- / Site Reliability Engineer (m / w / d)
IT Sonix Custom DevelopmentLeipzig, DESupervisor (m / w / d) Service Controlling AurumTours
CHECK24 VergleichsportalLeipzig- Gesponsert
Leitung eines Blutspendezentrums
Haema Blut- und PlasmaspendedienstLeipzig, DESite Controller (w / m / d)
Straumann GroupLeipzig, GermanyService 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, GermanyClinical 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