Oncology Data Coordinator Stellenangebote


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8 Jobs für Oncology Data Coordinator


Stellenangebote Oncology Data Coordinator Jobs


Job vor 2 Tagen bei Jobleads gefunden

Clinical Trials Site Coordinator

• Zug [. .. ] Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. Please submit CV in English. Job Description [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP, protocol requirements within studyspecific defined timelines and enrollment goals. 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 and preparation for [. .. ] 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 sitespecific regulatory documents as needed. [. .. ] and medical research working in the role of a Study Coordinator or similar function. Upperintermediate 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 fastpaced environment, with short timelines and multiple tasks to be completed simultaneously. Ability to effectively communicate in stressful situations and demonstrate the ability to problemsolve in an effective and efficient manner. Flexibility in working hours may be [. .. ]

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Job am 17.02.2026 bei Jobleads gefunden

Associate Director, Trial Clinical Delivery Lead (all genders)

• Eysins, Waadt Führungs-/ Leitungspositionen [. .. ] United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic [...]
MEHR INFOS ZUM STELLENANGEBOT[...] areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across [. .. ] in collaboration with Clinical Trial Leads (CTLs) and Contract Research Organizations (CROs) , using a riskbased quality management approach. Continuously update the strategy based on external changes and new internal data. Utilize site performance and quality data analytics to drive proactive, riskbased site oversight practices and quality risk oversight and management across all stages of study delivery. Develop, implement, and follow up on robust Site Oversight Plans, in collaboration with the CTL (s) and working closely with the respective CSLs. Identify [. .. ] quality/ costs) and work with CSLs, CTLs, Data Managers, Clinical Lead (s) and other relevant business partners to implement action plans to resolve and/or mitigate. Participate in Investigator/ Study Coordinator Meetings and promote information sharing with the CSLs as needed. Travel: Position may require domestic/ international travel up to 20 of time. Who you are Minimum Requirements Bachelors Degree Medical or Life Sciences degree in a clinical research related discipline 8-10 years professional and project management experience in delivering [. .. ]

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Job am 14.02.2026 bei Jobleads gefunden Associate Director, Trial Clinical Delivery Lead (all genders) • Eysins, Waadt Führungs-/ Leitungspositionen [. .. ] United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic [...]
MEHR INFOS ZUM STELLENANGEBOT[...] areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across [. .. ] in collaboration with Clinical Trial Leads (CTLs) and Contract Research Organizations (CROs) , using a riskbased quality management approach. Continuously update the strategy based on external changes and new internal data. Utilize site performance and quality data analytics to drive proactive, riskbased site oversight practices and quality risk oversight and management across all stages of study delivery. Develop, implement, and follow up on robust Site Oversight Plans, in collaboration with the CTL (s) and working closely with the respective CSLs. Identify [. .. ] quality/ costs) and work with CSLs, CTLs, Data Managers, Clinical Lead (s) and other relevant business partners to implement action plans to resolve and/or mitigate. Participate in Investigator/ Study Coordinator Meetings and promote information sharing with the CSLs as needed. Travel: Position may require domestic/ international travel up to 20 of time. Minimum Requirements Bachelors Degree Medical or Life Sciences degree in a clinical research related discipline 8-10 years professional and project management experience in delivering Clinical Operations of [. .. ]

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Job vor 6 Tagen bei Neuvoo gefunden Sirtex

Planning Logistics Coordinator (m, f, d)

• Frankfurt, Hessen Work-Life-Balance [. .. ] provide weekly manufacturing plans, indicating when production teams should execute specific production builds. Complete all associated ERP transactions to prepare for production. Follow guidelines provided by site [...]
MEHR INFOS ZUM STELLENANGEBOT[...] manufacturing leadership and data analytics to achieve optimal production schedules that minimizes Y90 costs while ensuring on time delivery and product availability requirements are met. Responsible for weekly Y90 procurement to fulfill manufacturing demands as well as working with the data analytics team to define the best overall purchasing schedule. Identify areas of cost [. .. ] support ongoing professional growth through career development, on the job experiences and training opportunities. Challenging work which supports the development of new and better ways to improve clinical outcomes for oncology treatment around the world. An unwavering commitment to company values, employee safety and excellence in everything we do. Diversity drives innovation; inclusion fosters belonging, growth and success. Sirtex believes that it takes multiple perspectives and voices to create a culture and workplace which fosters engagement, teamwork, and employee satisfaction to [. .. ]

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Job vor 7 Tagen bei Neuvoo gefunden Georgetown University in Qatar

Clinical Research Nurse

• Ingelheim am Rhein, Rhineland- Palatinate Work-Life-Balance [. .. ] a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job Overview Serves as Clinical Research Nurse 1 for the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Cellular Therapy Program oncology clinical trials conducted in the Lombardi Clinical Trials Office of the Lombardi Comprehensive Cancer Center at Georgetown University. Additional duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Collaborate with investigators and more senior study team members by participating in recruitment and selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements. Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines. Coordinate or conduct study-related procedures and assessments while maintaining protocol integrity and patient safety and in accordance with Good Clinical Practice [. .. ] trials. Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators. Collaborate with Data Coordinator (s) to assure the documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Document and report serious adverse events per protocol and institutional policy. Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Act [. .. ]

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Job am 12.02.2026 bei Neuvoo gefunden Bei Gene

Business Operations Director, Germany

Führungs-/ Leitungspositionen [. .. ] ANALYTICS Define and monitor KPIs reporting frameworks and support the implementation of digital tools and business analytics dashboards to ensure visibility and accountability for operational and commercialization [...]
MEHR INFOS ZUM STELLENANGEBOT[...] performance tracking. Provide data-driven insights to support informed decision-making across business operations and field activities. In collaboration with above-country groups, drive Medical Excellence Sales Force Effectiveness (SFE) processes, including activity tracking, performance monitoring, target setting support and incentive-related analytics. Develop and lead innovative solutions for healthcare (ISH) creating added value [. .. ] development to ensure the teams operational readiness and resilience. Provide feedback, advice project updates and encouragement to team members Supervisory Responsibilities: Manages training and or Innovation Solution Manages the Country coordinator team Manages Congress Events Manages country business analytics Manages project management Qualifications Capabilities Experience in Oncology or Hemato-Oncology is highly desirable +10 years of qualified work experience in project management and related operations management areas and demonstrable planning, project management and analytical skills Demonstrated success in driving operational excellence in pharma companies Highly self-motivated, solution-oriented with an ability to work both with light-[. .. ]

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Job am 06.02.2026 bei Neuvoo gefunden Georgetown University in Qatar

Research Data Coordinator I

• Ingelheim am Rhein, Rhineland- Palatinate Work-Life-Balance [. .. ] knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Overview The Research Data Coordinator I position is responsible for data management for phase I, II, and III oncology clinical trials conducted within the Clinical Research Management Office (CRMO) of the Lombardi Comprehensive Cancer Center (LCCC) . Additional duties include, but are not limited to: Supports all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO) , including collection of [. .. ]

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Job am 23.01.2026 bei Neuvoo gefunden Georgetown University in Qatar

Clinical Research Nurse II

• Ingelheim am Rhein, Rhineland- Palatinate Work-Life-Balance [. .. ] a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job Overview Serves as Clinical Research Nurse 2 for the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Cellular Therapy Program oncology clinical trials conducted in the Lombardi Clinical Trials Office of the Lombardi Comprehensive Cancer Center at Georgetown University. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Collaborate with investigators and more senior study team members by participating in recruitment and selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements. Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines. Coordinate or conduct study-related procedures and assessments while maintaining protocol integrity and patient safety and in accordance with Good Clinical Practice [. .. ] trials. Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators. Collaborate with Data Coordinator (s) to assure the documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Document and report serious adverse events per protocol and institutional policy. Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Act [. .. ]

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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 8 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 Rheinland-Pfalz (3 Jobs), Hessen (1 Jobs) und Sachsen-Anhalt (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Oncology Data Coordinator Jobs?

Oncology Data Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.


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