11 Jobs für Clinical Trials Supervisor
Stellenangebote Clinical Trials Supervisor Jobs
Job vor 6 Tagen 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 vor 14 Tagen bei Jobleads gefunden
• 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 Lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 04.12.2025 bei Jobleads gefunden
Country Medical Lead, Switzerland Austria (remote)
• 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 Insulets affiliate. [. .. ] 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 in-country Medical Affairs colleagues to lead the development of robust [. .. ] 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 peer-to-peer scientific relationships with national and regional KOLs Build confidence and advocacy [. .. ]
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 [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] safety. We are currently searching a Senior Manager Medical Affairs (m/f/d) based in Munich. Summary The Global Manager Sr. Medical Affairs-HST (Manager MA HST) will provide both [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development and launch expertise as well as technical knowledge to assigned product line (s) of appropriate HST division. This person is responsible for aligning their team with HST Medical Affairs and other pertinent departments. Critical to this role is global and regional clinical knowledge of surgical medical devices environments of [. .. ] legal and regulatory and quality requirements related to R D and product lifecycle management. Maintains compliance with current standard operating procedures. Assumes other duties and responsibilities as assigned by manager/ supervisor. Clinical core competency for related products. Technical core competency for related products. Legal and regulatory core competency for related products. KEY QUALIFICATIONS Excellent written oral communication and organizational skills. Effective and competent presentation and teaching skills. Self-motivated independent mulit-tasking team-oriented individual with exceptional follow through. -Industry experience [. .. ] or financial information. To learn how you can protect yourself review our Recruitment Fraud Notice. Required Experience Senior Manager 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 Vacancy: 1 #J-18808-Ljbffr 70789416 [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
TFS Health Science
• Essen, North Rhine- Westphalia
About this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate corrective actions as directed by the supervisor Contribute to Ethics Committee/ IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
TFS Health Science
Senior Clinical Research Associate
• Munich, Bavaria
About this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate corrective actions as directed by the supervisor Contribute to Ethics Committee/ IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
TFS Health Science
Senior Clinical Research Associate
• Hamburg
About this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate corrective actions as directed by the supervisor Contribute to Ethics Committee/ IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
TFS Health Science
Senior Clinical Research Associate
• Kassel, Hessen
About this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate corrective actions as directed by the supervisor Contribute to Ethics Committee/ IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
TFS Health Science
Senior Clinical Research Associate
• Mainz, Rhineland- Palatinate
About this role TFS Health Science is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. As part of our SRS/ FSP team, you will be dedicated to one sponsor. Please, keep in mind that this is a Freelance opportunity for approximately 0.7 FTE with sites in both Germany and Switzerland. Key Responsibilities Monitor clinical trials on-site and remotely in accordance with TFS/ client SOPs, FDA regulations, and GCP/ ICH guidelines Review CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issues Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA Initiate corrective actions as directed by the supervisor Contribute to Ethics Committee/ IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/ Project Manager Participate in contract handling and negotiation under direction of the Lead CRA/ Project Manager Set up the Investigator Site File (ISF) and Study Master File [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
Insulet Corporation
Country Medical Lead, Switzerland Austria (remote)
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 Leadfor Switzerland Austriaisaccountablefor developing and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] executingthe Medical Affairs strategyforthe2countries. They lead the creation and execution ofthecountry medical plansin alignment with the businessobjectivesof the Insuletsaffiliate. Themedical plansencompassvalue-generating activities onmedicaleducation, evidence generation and dissemination, HCP and KOL engagement, andinternalknowledge and insights [. .. ] advocacy organizations areidentifiedand met. One of theprioritiesfor this individual will bekey opinion leader (KOL) engagementand local evidence generation. This includes establishing, fostering, cultivatingandmaintainingrelationships with KOLs as a conduit foraccurateand updated clinical, scientificand 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 andotherin-country Medical Affairscolleagues to lead the development of robustcountrylaunch plansfor newproducts, andexecutesthem with [. .. ] training with generation and delivery of medical content Inform strategize evidence generation plans, in answer tofulfilmarket access, regulatory and marketing needs Support the local execution of Insulet-sponsored and Investigator-Initiated trials Disseminate evidencewithin local markets Identifyand engage with HCP to inform and seek advice on the companys solutions, through the execution of advisoryboards, clinical activity, scientific Exchangeandeducational Events Establish andmaintaincredible peer-to-peer scientific relationships with nationaland regional KOLs Build confidence and advocacy among key external influencers (KOLs) Build and share knowledge [. .. ]
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 11 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 (2 Jobs), Niedersachsen (1 Jobs) und Nordrhein-Westfalen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Supervisor Jobs?
Clinical Trials Supervisor Jobs gehören zum Berufsfeld Biotechnologie.
