8 Jobs für Clinical Trials Supervisor
Stellenangebote Clinical Trials Supervisor Jobs
Neu Job vor 6 Std. bei Jobleads gefunden
• Zürich Zuerich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 2 Tagen bei Jobleads gefunden
• Zürich Zuerich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 79640993 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Doctoral student position-Evaluating novel mineral sources for treatment of micronutrient def. . .
• Zürich Zuerich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. ) Please note that applications without these documents will not be considered. More information about our research can be found at the website of Sustainable Food [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Doctoral student position Evaluating novel mineral sources for treatment of micronutrient def. . .
• Schaffhausen, Zürich Zuerich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. We would like to point out that the pre-selection is carried out by the responsible recruiters and not by artificial intelligence. ETH Zurich is one [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Burgenland
Job Title: Sr. Medical Affairs Manager, Switzerland Austria (CH/ AT) Department: Medical Affairs Manager/
Supervisor: Medical Affairs Director, Europe FLSA Status: Exempt Position Overview The Medical Affairs Lead for Switzerland [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Austria is accountable for developing and executing the Medical Affairs strategy for the 2 countries. They lead the creation and execution of the country medical plans in alignment with the business objectives of the Insulets [. .. ] this individual will be key opinion leader (KOL) engagement and local evidence generation. This includes establishing, fostering, cultivating and maintaining relationships with KOLs as a conduit for accurate and updated clinical, scientific and medical information between KOLs and the company. The person will also ensure local evidence is being generated, fulfilling local needs and in alignment with the global evidence generation strategy. This role works closely with Global and other incountry Medical Affairs colleagues to lead the development of robust country [. .. ] and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insulet-sponsored and Investigator-Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy among key [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 10.12.2025 bei Jobleads gefunden
Country Medical Lead, Switzerland Austria (remote)
• Füssen, Bayern
Job Title : Sr. Medical Affairs Manager, Switzerland Austria (CH/ AT) Department : Medical Affairs Manager/
Supervisor: Medical Affairs Director, Europe FLSA Status: Exempt Position Overview The Medical Affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Lead for Switzerland Austria is accountable for developing and executing the Medical Affairs strategy for the 2 countries. They lead the creation and execution of the country medical plans in alignment with the business objectives of the Insulets [. .. ] this individual will be key opinion leader (KOL) engagement and local evidence generation. This includes establishing, fostering, cultivating and maintaining relationships with KOLs as a conduit for accurate and updated clinical, scientific and medical information between KOLs and the company. The person will also ensure local evidence is being generated, fulfilling local needs and in alignment with the global evidence generation strategy. This role works closely with Global and other incountry Medical Affairs colleagues to lead the development of robust country [. .. ] and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insulet-sponsored and Investigator Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy among key [. .. ]
Job am 03.12.2025 bei Jobleads gefunden
Country Medical Lead, Switzerland Austria (remote)
• Schwyz
[. .. ] (remote) Join to apply for the Country Medical Lead, Switzerland Austria (remote) role at Insulet Corporation Job Title: Sr. Medical Affairs Manager, Switzerland Austria (CH/ AT) Department: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Affairs Manager/ Supervisor: Medical Affairs Director, Europe FLSA Status: Exempt Position Overview The Medical Affairs Lead for Switzerland Austria is accountable for developing and executing the Medical Affairs strategy for the 2 countries. They lead the creation and execution of the country medical plans in alignment with the business objectives of the Insulets [. .. ] this individual will be key opinion leader (KOL) engagement and local evidence generation. This includes establishing, fostering, cultivating and maintaining relationships with KOLs as a conduit for accurate and updated clinical, scientific and medical information between KOLs and the company. The person will also ensure local evidence is being generated, fulfilling local needs and in alignment with the global evidence generation strategy. This role works closely with Global and other incountry Medical Affairs colleagues to lead the development of robust country [. .. ] and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution of Insulet-sponsored and Investigator-Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy among key [. .. ]
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 8 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 Bayern (1 Jobs), Sachsen (1 Jobs) und Hessen (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Supervisor Jobs?
Clinical Trials Supervisor Jobs gehören zum Berufsfeld Biotechnologie.
