3 Jobs für Oncology Data Coordinator
Stellenangebote Oncology Data Coordinator Jobs
Job vor 5 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. Job Description [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling [. .. ] support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the site level. Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. Proper handling, accountability and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all site-specific regulatory documents as [. .. ] medical research working in the role of a Study Coordinator or similar function. Upper-intermediate level of English, with the ability to work in a global team environment. Experience in Oncology, Renal, or Cardiology clinical studies is a plus. Ability to work in a fast-paced environment, with short timelines and multiple tasks to be completed simultaneously. Ability to effectively communicate in stressful situations and demonstrate the ability to problem-solve in an effective and efficient manner. Flexibility in working hours [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
• Deutschland Deutschland, DE
[. .. ] include ensuring the safety and well-being of study participants at assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations [. .. ] process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. , Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trial-related systems and procedures, regulations and GCPs, and the scientific/ clinical knowledge to be able to understand the nature of drugs being studied Excellent written and verbal communication skills, and time management, organizational and problem-solving skills Fluent in [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate-Germany
• München, Bayern
[. .. ] include ensuring the safety and well-being of study participants at assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations [. .. ] process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. , Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trialrelated systems and procedures, regulations and GCPs, and the scientific/ clinical knowledge to be able to understand the nature of drugs being studied Excellent written and verbal communication skills, and time management, organizational and problemsolving skills Fluent in German language [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Oncology Data Coordinator pro Jahr?
Als Oncology Data Coordinator verdient man zwischen EUR 45.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Oncology Data Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 3 offene Stellenanzeigen für Oncology Data Coordinator Jobs.
In welchen Bundesländern werden die meisten Oncology Data Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Oncology Data Coordinator Jobs werden derzeit in Sachsen (1 Jobs), Bayern (1 Jobs) und Nordrhein-Westfalen (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Oncology Data Coordinator Jobs?
Oncology Data Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
