Clinical Monitoring Jobs in München
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Suchergebnisse - Clinical Monitoring Jobs in München
ThermoFisher-München
for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient...
Direct Staffing Inc-München
Director, Budgeting / Monitoring - Patient Care Services
• Full-time
Director, Budgeting / Monitoring - Patient Care Services
Healthcare / Health Services - Other
Exp 2-5 yrs
Relo
Bonus
Job Description
Provides strategic leadership for...
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ThermoFisher-München
purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Our global Clinical Monitoring department consists of colleagues with...
Integrated Resources Inc.-München
Risk-based Monitoring (ARBM) group and for the medical reviewers in the iDARTs application (an internally developed tool for medical review of clinical trial data based on TIBCO’s Spotfire).
PRINCIPAL RESPONSIBILITIES: % OF TIME
• Visualizations for...
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Allucent-München
in patients’ lives.We are looking for a Senior Clinical Research Associate to join our team in GermanyThe Sr CRA will be responsible for the following tasks:Governs quality standards for trial monitoring activities.Performs Selection, Initiation, Monitoring...
Medpace, Inc.-München
CRA, CRA Manager, Clinical Trial Manager
• Casual Dress Code
Responsibilities
• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site...
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Daiichi Sankyo Europe GmbH-München
Clinical Trial Business Operations Performance and Delivery, and Alliance Strategic Vendor Oversight (SVO)) to monitor Europe's performance as planned, including mitigation strategies.
• Function as a key point of escalation for issues and problem...
stepstone.de -
Pharmiweb-München
these throughout the study.
Interact/train new investigators to work on the client clinical trials
Attend key therapeutic trainings/meetings and/or industry trainings
Qualifications:
SCRA with a minimum of 4+ years of monitoring experience...
mapmeo.com -
Daiichi Sankyo Europe GmbH-München
development of safety monitoring plan, effective implementation of safety monitoring activities, Benefit/Risk assessment with appropriate risk minimization activities, and effectively communicates with internal and external stakeholders, within the framework...
stepstone.de -
Exact Sciences-München
Help us change lives
At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to...
Daiichi Sankyo Europe GmbH-München
statistical contact for the assigned study activities, in particular in cross-functional Study team(s).
Aufgaben
• Responsible for a clinical study: provide input on the development of study protocol (design, sample size, statistical analysis strategy...
stepstone.de -
Medpace-München
monitoring, and closeout visits for research sites in compliance with the approved protocol;Communication with the medical site staff including coordinators, clinical research physicians and their site staff;Verifying adequate investigator qualifications...
Direct Staffing Inc-München
RN DIRECTOR CLINICAL QUALITY IMPROVEMENT
• Full-time
Hospital
RN DIRECTOR CLINICAL QUALITY IMPROVEMENT
5+ to 7 years experience
• The Director of Clinical Quality Improvement (DCQI), a key member of the hospital management team, is responsible...
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Daiichi Sankyo-München
Clinical Safety Scientist Lead, Clinical Safety Physician(s), PSL, and cross-functional team to develop safety strategy, key safety messages, and review and author safety sections of CTDDevelop expertise in one or more focus areasSupports Data Monitoring...
Integrated Resources Inc.-München
monitoring plans, abstracts, presentations, manuscripts and clinical study reports.
• May assist in compilation of investigator brochures under close supervision.
• Assists in preparation of safety, interim and final study reports, including resolving data...
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