7 Jobs für Regulatory Writing in Stuttgart
Stellenangebote Regulatory Writing in Stuttgart Jobs
Job am 17.10.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program. Lead development of clinical sections of trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and program level regulatory documents such as protocol amendments, imaging/ pathology/ DSMB charters, briefing books, BLA/ MAA, ODD, breakthrough applications etc. Act as clinical lead within the clinical trial team (CTT) and support the other CTT functions such as biostats/ Dm/Pharmacology/ PV/ Clinical operations etc. Execute the clinical development strategy in accordance with [. .. ] of experience in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
[. .. ] on track. Support feasibility assessments, site selection, initiation, routine monitoring, and closeout visits. Provide mentorship to junior CRAs and contribute to best practice development. Prepare study reports [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and maintain essential regulatory documentation. Partner with crossfunctional teams (Regulatory, Project Management, Data Management, Safety) . Contribute to inspection readiness and support regulatory audits as needed. Requirements 35+ years of independent monitoring experience as a CRA, with solid exposure to complex, interventional studies. Direct experience in cell gene therapy trials (e. g. , CART, [. .. ] bodies for our commitment to excellence and service delivery. We have extensive functional expertise including : Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/ Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ belief, sexual orientation or age. #J-18808-Ljbffr 72577882 [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Homeoffice möglich
[. .. ] Y Combinator. As one of the fastestgrowing tech companies, bringing together earlystage engineers, product builders, and business athletes from companies like Stripe, Airbnb, and Shopify. Were tackling [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deep technical and regulatory challenges to make connectivity truly seamless. If youre driven by curiosity, creativity, and the chance to shape the future of telecom, wed love to hear from you. The Role You will help build Connect, our consumerfacing hosted checkout and subscription management service, and related projects to deliver the best experience [. .. ] are able to implement the best possible UX. You have built and maintained scalable apps. You love to build things for scale and have experience in designing app architectures and writing highquality code. You enjoy building a product from scratch. This means high involvement in the design process and understanding what customers want and users need. You love learning technologies as you go. You always want to find the right tool for the job, and not only follow what you already [. .. ]
Job vor 8 Tagen bei Neuvoo.com gefunden
Sanofi EU
• Stuttgart
[. .. ] units within other Sanofi sites, and other organizations within the External Manufacturing and Supply and Specialty Care network (e. G. procurement, supply chain, finance) to ensure compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with internal and regulatory requirements, and to disposition intermediates (e. G. API, drug substance) and finished products with minimal risk to quality or product supply. EM S LM SC has responsibility for CMO and CLO and distribution activities related to products treating Rare Diseases and Rare Blood Disorders, Multiple Sclerosis (MS) , and Oncology EM [. .. ] with an understanding of worldwide regulatory affairs Demonstrated ability to perform work that consistently requires independent decision making and the exercise of independent judgment and discretion Problem solving and technical writing skills Ability to multitask effectively Willingness to travel Languages: Good written and verbal communication in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team Discover endless opportunities to grow your talent and drive your career, whether its through a promotion or lateral move, [. .. ]
Job am 30.11.2025 bei Neuvoo.com gefunden
Buckden Partners
• Stuttgart
[. .. ] portfolio risk management for the companys commercial real estate (CRE) lending activities across the UK and selected European jurisdictions. This role ensures that all lending decisions are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] robust, compliant with regulatory requirements, and aligned with the companys strategic objectives. The Credit Manager will partner with origination, legal, and senior management teams to support business growth while maintaining prudent credit standards. Responsibilities: Credit Analysis Underwriting Lead the evaluation of complex CRE lending opportunities, including development finance, investment loans, and bridging facilities. Analyse [. .. ] risk, lending, or underwriting with experience of property lending (CRE or Development Finance) . Strong understanding of secured loan structures, real estate assets, and legal documentation. Excellent analytical and credit writing skills with the ability to present clear, concise recommendations. Confident working in a fast-paced environment and managing multiple priorities simultaneously. Proven ability to challenge assumptions and take ownership of decisions. Strong interpersonal skills and a collaborative approach to cross-functional work. Degree-educated or equivalent; relevant professional qualifications a [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
• Stuttgart
[. .. ] oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Participate in the start-up of global clinical studies, working with Clinical Operations to ensure on schedule site activation and subject enrollment, monitoring, compliance with safety practices, policies, procedures as well as the day-[. .. ] and mitigate risk. These may include meeting timelines in site activation, enrollment, identifying shortcomings or delays in data entry at clinical sites, and ensuring the timely execution of responses to regulatory interactions. Play a key role in the review of study data to ensure timely and high-quality data entry, including review of case report forms, assists in coding, analysis, and proper and complete documentation of clinical data. Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Associate Medical Director/ Medical Director
• Stuttgart
Führungs-/ Leitungspositionen
[. .. ] clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program. Lead development of clinical sections of trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and program level regulatory documents such as protocol amendments, imaging/ pathology/ DSMB charters, briefing books, BLA/ MAA, ODD, breakthrough applications etc. Act as clinical lead within the clinical trial team (CTT) and support the other CTT functions such as biostats/ Dm/Pharmacology/ PV/ Clinical operations etc. Execute the clinical development strategy in accordance with [. .. ] of experience in a pharmaceutical or biotechnology environment and experience in biologics/ ADC clinical development. Strong track record of working within clinical teams in global Phase I-IV trials. Experience writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. Holds a working knowledge of oncology with a proven track record to interpret, discuss and present efficacy safety data relating to clinical trials. Solid understanding of GCP, clinical trial design, statistics, and regulatory and [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Regulatory Writing pro Jahr?
Als Regulatory Writing verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Regulatory Writing Jobs in Stuttgart bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 7 offene Stellenanzeigen für Regulatory Writing Jobs in Stuttgart.
Zu welchem Berufsfeld gehören Regulatory Writing Jobs in Stuttgart?
Regulatory Writing Jobs in Stuttgart gehören zum Berufsfeld Technische Dokumentation / Redaktion.
