5 Jobs für Clinical Trials Supervisor
Stellenangebote Clinical Trials Supervisor Jobs
Job am 06.03.2026 bei Jobleads gefunden
• Wiesbaden, Hessen
Overview Velocity
Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our [...]
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[...] values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step. Job Summary The Manager, Site Operations is responsible for managing the clinical operations staff, training and onboarding of new staff, managing quality and compliance of clinical work closely with and in support of the Site Director. Able to perform coordinator as well as supervisor duties and fill in during the absence of site coordinators. Able to function as lead coordinator on select protocols. Must be able to work independently and with all staff and customer levels. Responsibilities Work with the Site Director to meet/ exceed the sites financial, operational and study-specific targets. Support [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
At Smartways, we specialise in timecritical, complex logistics for the Australasian healthcare community. What we do directly supports patient outcomes and saves lives across medical devices, life sciences, pharmaceuticals, and [...]
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[...] clinical trials. Our people are passionate, resilient, and driven by purpose and we are looking for an AM Operations Team Leader who thrives in fastpaced, highimpact environments. The Opportunity As the AM Operations Team Leader, you will play a critical role in ensuring the smooth execution of morning operations across Queensland. You [. .. ] is innovating, sustainable, and futurefocused. Application Questions Which of the following statements best describes your right to work in Australia? How many years experience do you have as an operations supervisor? Do you have experience working with logistics, freight delivery services? Do you have a current Australian drivers licence? Which of the following Microsoft Office products are you experienced with? Whats your expected annual base salary? #J-18808-Ljbffr 82184166 [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
• Zürich
Werkstudenten
[. .. ] student on the topic of Novel sources of minerals for treatment of micronutrient deficiencies in humans, focusing on investigating the absorption and bioavailability of novel mineral sources [...]
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[...] in vivo in clinical trials. Project background Micronutrient deficiency is a widespread global health problem, primarily driven by inadequate dietary intake. More than 5 billion people are estimated to not consume enough of at least one micronutrient. Among those, mineral deficiencies can be particularly critical, namely, iron, calcium, zinc, and magnesium deficiencies, which are particularly [. .. ] language) , if possible and not confidential If you havent completed your MSc studies at the time of submission, please substitute the MSc diploma with a written statement by your supervisor specifying the expected completion date and confirming that you are expected to finish on time and send the most recent draft of your thesis. #J-18808-Ljbffr 79884571 [. .. ]
Job am 18.12.2025 bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] responsible for leading regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of U. S. and international regulatory submission strategies. Responsibilities Formulate CMC [...]
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[...] regulatory strategies without supervisor oversight based on current regulatory intelligence. Collaborate with crossfunctional project teams and external business partners to develop CMC regulatory strategies and identify regulatory risks, representing the department in crossfunctional project teams. Identify required documentation and any content quality and timeline issues for global submissions and manage the delivery of approved technical documents in accordance with project timelines. Manage the preparation, authoring, and maintenance of regulatory submission documents pertaining to CMC data for global clinical trial and marketing applications as well as postmarketing variations. May require technical regulatory authoring of submission package components. Support the evaluation of manufacturing changes for potential impact on products. Provide expert review of CMC documentation supporting regulatory submissions and communications. Coordinate preparation of responses to queries from regulatory authorities, particularly [. .. ] outside partners. Excellent oral and written communication skills. Excellent organizational skills and attention to detail. Hybrid Work #LIHYBRID Key Skills Proofreading Adobe Acrobat FDA Regulations Manufacturing Controls Biotechnology Clinical Trials Research Development GLP c GMP Product Development Chemistry Writing Skills Employment Type Full Time Experience Years: 1012 Vacancy 1 Equal Opportunity Employer Cytokinetics is an Equal Opportunity Employer. Fraud Warning Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
WCG Clinical
• Frankfurt am Main, Hessen
[. .. ] projected contribution rates, allowing sponsors to make informed decisions, thereby effectively de-risking the study and accelerating timelines. This role also includes the placement and management of qualified [...]
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[...] medical staff (Clinical Research Coordinators) inhealthcare organizations (HCOs) participating in clinical trials within their respective country (ies) . EDUCATION REQUIREMENTS: Bachelors degree in the sciences, marketing, or business; or equivalent education/ relevant experience. QUALIFICATIONS/ EXPERIENCE: At least 2 years of project managementor sales experience within the healthcare industry (medical device, pharmaceutical, managed care, etc. ) , clinical trial recruitment and/or other [. .. ] accordance with WCGs Standard Operating Procedures and methodologies, Good Clinical Practice, European General Data Protection regulations and local country anti kick-back anti-bribery regulations. Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here. Attendance and punctuality are essential functions of the position. TRAVEL REQUIREMENTS: 0 5 5-10 10-20 20-50 50 Physical and Sensory Requirements: The physical and sensory requirements described here are representative of those that must be met [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Supervisor pro Jahr?
Als Clinical Trials Supervisor verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Supervisor Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 5 offene Stellenanzeigen für Clinical Trials Supervisor Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Supervisor Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Supervisor Jobs werden derzeit in Hessen (2 Jobs), Sachsen-Anhalt (2 Jobs) und Sachsen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Supervisor Jobs?
Clinical Trials Supervisor Jobs gehören zum Berufsfeld Biotechnologie.
