77 Jobs für Investigational
Stellenangebote Investigational Jobs
Job am 23.03.2026 bei StepStone gefunden
Otsuka Pharma GmbH
• Frankfurt am Main
Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten
[. .. ] as soon as possible as Associate Director Global Regulatory Affairs (m/f/d) The Associate Director Regulatory Affairs provides global regulatory expertise to pre-clinical, clinical, and commercial areas for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] investigational and marketed products and he ensures that regulatory/ competitive intelligence, or scientific/ regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. Furthermore the Associate Director Regulatory Affairs collaborates with Regulatory Management to establish clear regulatory pathways and creates accurate and timely documents for submission and final [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Novartis
Drug Product Project Leader (m/f/d) Associate Director Science Technology
• AT- 7 Langkampfen
Führungs-/ Leitungspositionen
[. .. ] drug product formulation and process development, technology transfers and regulatory submissions Proficient in quality principles, Quality by Design (Qb D) , Good Manufacturing Practice (GMP) and regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requirements with experience in Investigational New Drug (IND) / Biologics License Application (BLA) submissions Excellent leadership and interdisciplinary skills, with a track record of leading cross-functional global teams and projects Excellent project management, communication/ presentation, stakeholder management and scientific/ technical writing skills Openness to digital transformation and proactiveness in adopting new digital tools and [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare [. .. ]
Job am 14.03.2026 bei Mindmatch.ai gefunden
PSI CRO
Clinical Site Coordinator
• AT- 9 Wien
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and reconciliation of investigational products and clinical supplies. Collect, handleand maintainall site-specific regulatory documents as needed. Facilitateand support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Scheduleand/or performstudy procedures as per study requirements and delegation of responsibilities. Preparefor and participatein onsite study [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture. Verifies site compliance with electronic data capture [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/ local regulations and organizational procedures to ensure IP is [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA single sponsor-Germany
• AT- 9 Wien
[. .. ] agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/ local regulations and organizational procedures to ensure IP is [. .. ]
Job am 20.02.2026 bei Mindmatch.ai gefunden
Sandoz International GmbH
• AT- 7 Kundl
Teilzeit
[. .. ] company based in Austria is looking for a Senior Regulatory Specialist (d/f/m) on a part-time basis. The role focuses on developing and implementing global labeling strategies for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] investigational and marketed products. Candidates should have a scientific academic degree and strong communication skills, while experience in regulatory affairs is a plus. This position offers attractive benefits including flexible working hours and opportunities for professional growth. J-18808-Ljbffr 81242175 [. .. ]
Job am 20.02.2026 bei Mindmatch.ai gefunden
Sandoz International GmbH
Senior Regulatory Specialist (d/f/m) Part-Time 80
• AT- 7 Kundl
Teilzeit Homeoffice möglich
[. .. ] product lifecyclefrom development to post-authorization. Please note that this is a part-time position (80) . Your Key Responsibilities: Develop and implement global labeling and artwork strategies for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] both investigational and marketed products, ensuring alignment with regulatory requirements and product development timelines. Provide regulatory input into safety risk communication and portfolio stewardship initiatives, with a focus on labeling implications. Conduct comprehensive assessments of labeling topics, including comparative analysis of reference and competitor product labeling, regulatory frameworks. Evaluate country-specific labeling [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Langkampfen, Tirol
Führungs-/ Leitungspositionen
[. .. ] drug product formulation and process development, technology transfers and regulatory submissions Proficient in quality principles, Quality by Design (Qb D) , Good Manufacturing Practice (GMP) and regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requirements with experience in Investigational New Drug (IND) / Biologics License Application (BLA) submissions Excellent leadership and interdisciplinary skills, with a track record of leading cross-functional global teams and projects Excellent project management, communication/ presentation, stakeholder management and scientific/ technical writing skills Openness to digital transformation and proactiveness in adopting new digital tools and [. .. ]
Job am 24.03.2026 bei Jobleads gefunden
Clinical Trials Site Coordinator
• Zug
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Homeoffice möglich
[. .. ] product lifecyclefrom development to post-authorization. Please note that this is a part-time position (80) . Your Key Responsibilities Develop and implement global labeling and artwork strategies for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] both investigational and marketed products, ensuring alignment with regulatory requirements and product development timelines. Provide regulatory input into safety risk communication and portfolio stewardship initiatives, with a focus on labeling implications. Conduct comprehensive assessments of labeling topics, including comparative analysis of reference and competitor product labeling, regulatory frameworks. Evaluate country-specific labeling [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Executive Director, Global Medical Affairs
Führungs-/ Leitungspositionen
[. .. ] intelligence to the CMO and cross-teams including Opinion Leader Programming and Clinical Research and Development. Serve as a resource for addressing unsolicited medical questions about Solid Biosciences [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trials and investigational products, providing current, fair-balanced medical and scientific information. Lead (in partnership with Opinion Leader Programming) the preparation and execution of regional and national advisory board meetings, delivering presentations, facilitating discussions, and capturing strategic insights to inform medical strategy and launch readiness. Provide clinical and scientific expertise in the development, [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
[. .. ] States on a full-time basis (no sponsorship) Preferred: Masters or higher degree (e. g. , Pharm D, Ph D) Skills Preferred: Global clinical trials in the rare [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] disease area Preferred: Clinical/ investigational pharmacy with gene therapy products or clinical supply management Preferred: Experience in rare disease, otology, audiology, gene therapy, cellular therapy, and/or medical devices Preferred: Proven track record of successfully conducting/ supporting clinical trials and development activities Preferred: Understanding of drug development, regulatory processes, and clinical trial design Required/Preferred: [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
(Senior) Medical Science Liaison, Medical Affairs (EU) - Northwest Germany
• München, Bayern
Work-Life-Balance
[. .. ] communication skills. The MSL/ Sr MSL will conduct dynamic medical/ scientific exchange with members of the healthcare/ scientific community to generate insight and foster collaborations related to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] both approved and investigational assets within Genmabs Haematology and Oncology portfolio. The current role is for an MSL/ Sr MSL based in Northwest Germany focusing on gynaecological malignancies. This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] selects Regulatory vendor meetings in alignment with product programs and Regulatory-driven projects Maintain CTAs ensuring Agency compliance Review clinical documentation, including protocols, DSURs, Investigator Brochures, Investigator Packages [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and General Investigational Plans to ensure GCP and Agency compliance Lead teams in the development of briefing documents for EMEA Agency meetings Manage and direct contractors/ vendors as needed on programs. Keep current with EMEA Agency guidelines and regulations. Prepare comments on draft documentation sent out for consultation from the health authority. Contribute [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
(Senior) Medical Science Liaison, Medical Affairs (EU) - Southwest Germany
• München, Bayern
[. .. ] communication skills. The MSL/ Sr MSL will conduct dynamic medical/ scientific exchange with members of the healthcare/ scientific community to generate insight and foster collaborations related to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] both approved and investigational assets within Genmabs Haematology and Oncology portfolio. The current role is for an MSL/ Sr MSL based in Southwest Germany focusing on gynaecological malignancies. This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Führungs-/ Leitungspositionen
[. .. ] Lead the preparation of Benefit Risk Assessments for Kyowa Kirin products and provide appropriate support for implementation of the associated conclusions. Develop appropriate risk management strategies for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] marketed and/or investigational compounds ensuring that these are contained and implemented in appropriate way including Risk Management Plans. Ensure success of such activities by close liaison with Submission teams. Lead signal detection activities using data from all sources and bring medical expertise to drive Benefit Risk assessment reports, provide safety input for the [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Clinical Research Associate
• Darmstadt, Hessen
Homeoffice möglich
[. .. ] growing international hematology/ oncology Clinical Trials program. This is a full-time job. Job overview: The CRA is responsible for ensuring that the conduct of a clinical trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] at selected Investigational Sites is according to the currently approved protocol/ amendments, ICH GCP guidelines, the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between the Sponsor, the Investigator and other study personnel to build and [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Mendrisio, Tessin
[. .. ] of drugs of interest. Contribute to the design of clinical studies to ensure that they are scientifically sound and aligned with the objectives of the research, compile [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] information on the investigational product to inform clinical investigators of the drugs properties, clinical data and safety profile. Revise Clinical Study Reports of completed clinical trials. Keep updated on the evolving global regulatory environment (FDA, EMA, ICH, etc. ) in the clinical area of expertise and ensure that documents and submissions adhere to those [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Principal Scientist-Quality Control Chemical Testing Lab (m/w/d)
• Alzey, Rheinland- Pfalz
[. .. ] a technical authority in decisionmaking forums. Problem Solving Innovation: Lead the resolution of highly complex QC technical challenges, design and implement novel solutions or improvements, conduct rootcause [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analysis, and develop investigational testing protocols. Cross Functional Influence: Collaborate and influence across multiple functions (Manufacturing, QA, Regulatory, Product Development) to ensure QC considerations are integrated into broader business decisions. Regulatory Interface: Serve as an SME during regulatory inspections and audits, addressing complex technical questions and defending the scientific rationale of methods. Mentorship and [. .. ]
Job am 24.03.2026 bei Jobleads gefunden
Associate Director Global Regulatory Affairs (m/f/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Jobbeschreibung The Associate Director Regulatory Affairs provides global regulatory expertise to pre-clinical, clinical, and commercial areas for
investigational and marketed products and he ensures that regulatory/ competitive intelligence, or [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific/ regulatory information searching, summarization, assessment and dissemination are provided to the Otsuka organization. Furthermore the Associate Director Regulatory Affairs collaborates with Regulatory Management to establish clear regulatory pathways and creates accurate and timely documents for submission and final [. .. ]
Job am 22.03.2026 bei Jobleads gefunden
Quality Assurance Manager
• München, Bayern
[. .. ] as applicable. QA-Approval and follow-up Quality events from GMP relevant vendors (Deviations, OOX, Complaints, Quality Issues, CAPAs, Change Control) . QA release of Intermediates and Sponsor release [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Investigational Medicinal Product (e. g. for USA) Lead compilation of Product Specification Files in collaboration with the respective stakeholders as applicable. Central QA point of contact at Tubulis for external GMP vendors and partners incl. setting-up, negotiating and revising Quality Assurance Agreements (QAA) with GMP vendors First point of contact [. .. ]
Job am 22.03.2026 bei Jobleads gefunden
GPMO Project Manager CMC Lead (f/m/d)
• Garching bei München, Bayern
Führungs-/ Leitungspositionen Homeoffice möglich
Jobticket
[. .. ] be scientifically robust, compliant, and inspectionready Project Management expert for highly visible interdisciplinary projects In a function as Workteam Lead CMC for our pipeline projects you cover [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] all CMC/ IMP (Investigational Medicinal Product) topics together with your team and different stakeholders You will lead and coordinate your team of SMEs and connect the dots, keep the overview also in unclear situations, and continuously challenge quality, timelines and budget Create oversights, project and budget plans, presentations Trigger and facilitate steering decisions, provide [. .. ]
Job am 21.03.2026 bei Jobleads gefunden
Global Regulatory Affairs Executive Director, Vaccines
• Zug
Führungs-/ Leitungspositionen
A vaccine innovation company in Zug is seeking an Executive Director of Regulatory Affairs to develop and implement global regulatory strategies for clinical
investigational studies and commercialization of vaccines. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The ideal candidate must have extensive regulatory experience in the pharmaceutical industry, particularly in vaccine development. Responsibilities include serving as a primary contact with regulatory authorities and managing regulatory submissions. This leadership role offers competitive compensation and comprehensive benefits. #J-18808-Ljbffr 85212377 [. .. ]
Job am 18.03.2026 bei Jobleads gefunden
Biomarker Operations Therapeutic Area Leader
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] Clinical Operations Country Footprint. The Biomarker Operations Therapeutic Area Leader at Roche/ Genentech is responsible for the operational leadership, delivery excellence and innovation for maximizing R D [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] opportunities with biosamples, investigational devices and companion diagnostic strategies using a compliance and ethics mindset in alignment to Roches One Pharma Strategy. The role collaborates internally/ externally, to develop and leverage technology/ data analytics, and innovative practices to advocate and drive on best practices for collection, data generation, storage, reuse, and destruction biosamples. The [. .. ]
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Häufig gestellte Fragen
Wieviele offene Stellenangebote gibt es für Investigational Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 77 offene Stellenanzeigen für Investigational Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Investigational Jobs?
Aktuell suchen 27 Unternehmen nach Bewerbern für Investigational Jobs.
Welche Unternehmen suchen nach Bewerbern für Investigational Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Investigational Stellenangebote:
- Thermo Fisher Scientific (5 Jobs)
- ICON (4 Jobs)
- Milestone One (3 Jobs)
- Lilly (3 Jobs)
- IQVIA (3 Jobs)
- Sandoz International GmbH (2 Jobs)
In welchen Bundesländern werden die meisten Investigational Jobs angeboten?
Die meisten Stellenanzeigen für Investigational Jobs werden derzeit in Bayern (19 Jobs), Hessen (7 Jobs) und Sachsen-Anhalt (5 Jobs) angeboten.
