212 Jobs für Clinical Data Associate
Stellenangebote Clinical Data Associate Jobs
Job vor 2 Tagen bei StepStone gefunden
Mars Wrigley Confectionery UK Limited
• Viernheim
Führungs-/ Leitungspositionen
[. .. ] products and services span 90+ reference laboratories around the globe; in-house diagnostic laboratory instruments and consumables, including rapid assay diagnostic products and digital cytology services; local and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cloud-based data services; practice information management software and related software and support; veterinary imaging and technology; veterinary professional education and training; and board-certified specialist support services. About Mars: Mars is a family-owned business with more than 50 billion in global sales. We produce some of the worlds best-loved brands: [. .. ] The Mars Five Principles Quality, Responsibility, Mutuality, Efficiency and Freedom inspire our 150, 000 Associates into taking action every day towards creating the world we want tomorrow. This role bridges clinical and technical expertise with commercial acumen, ensuring our imaging solutions meet the evolving needs of veterinary professionals across Europe and APAC. You will lead a team of Commercial and Technical Product Managers and collaborate closely with commercial, service, and marketing teams. The Director will be accountable for portfolio strategy, roadmap [. .. ] track record in product management, and a passion for advancing imaging solutions that elevate veterinary diagnostics and pet health outcomes. Veterinary Medicine or Animal Science degree or a bachelors or associate degree in an equivalent field. 7+ years working in a product management, or similar role, ideally in the veterinary industry/ animal health industry Veterinary industry experience: direct experience in the veterinary industry whether in clinical practice, veterinary pharmaceuticals, diagnostics, or related fields is highly valued Customer centric mindset-a strong [. .. ]
Job vor 9 Tagen bei StepStone gefunden
Milteny GmbH
Clinical Trial Assistant (m f d)
• Bergisch Gladbach
Homeoffice möglich
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for
clinical professionals [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical [. .. ] at all stages. As a Clinical Trial Assistant, you will be supporting the Clinical Trial Manager in all aspects that are required to keep the quality and timeliness of study data and communication on a high level: You support the distribution and tracking of critical clinical documents and information, e. g. essential documents, study supplies, budgets, manuals, other site and subject related information and investigational product releases in collaboration with the study team. Next this, you support the preparation and submission [. .. ] of study-level communication to stakeholders and participate in internal team meetings, taking minutes and providing status updates. You have already gained experience in clinical research as a clinical trial associate, clinical research associate and/or clinical study coordinator in the pharmaceutical/ biotech industry and/or you are a holder of an academic degree in life sciences, natural sciences, or healthcare. Attention to detail comes naturally to you as well as being highly organized. You are are used to prioritize multiple [. .. ]
Job vor 13 Tagen bei Jobware gefunden
TRB Chemedica AG
• Feldkirchen bei München
Homeoffice möglich
30+ Urlaubstage
[. .. ] (m/w/d) Digital Marketing Manager Healthcare (m/w/d) Marketing Communications Manager Healthcare (m/w/d) Content Manager Healthcare/ Pharma (m/w/d) Commercial Product Specialist (m/w/d)
Clinical Product Manager (m/w/d) Medical Affairs Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (m/w/d) Scientific Product Specialist (m/w/d) Medical Science Liaison (m/w/d) (mit leichter Marketingnähe) Medical Content Specialist (m/w/d) Event Congress Manager Healthcare (m/w/d) Healthcare Communications Manager (m/w/d) Education Training Manager Medical Devices [. .. ] Content Strategist Content Creation Manager Pharma SEO/ SEA Manager Healthcare UX Content Manager Med Tech Healthcare E-Commerce Manager Digital Communications Manager Pharma Marketing Automation Specialist Healthcare Scientific Affairs Specialist Clinical Research Associate (mit Produktfokus) Medical Information Specialist Evidence Data Manager Healthcare Clinical Evidence Manager Med Tech Regulatory Product Communication Specialist Medical Event Manager Healthcare Training Coordinator Medical Congress Coordinator Education Specialist Medical Devices Health Communications Specialist Corporate Communications Manager Healthcare 71621652 [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Blueprint Medicines, a Sanofi company
Customer Experience Manager, North Germany
• hamburg
Location (s) : Berlin, Hamburg, Hannover (Germany) Level of position:
Associate Director Position type: 60 field-based, 40 (home-) office based Reporting Line: Marketing Lead Germany How will your role help [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us transform hope into reality? We are looking for a highly motivated and visionary personality who is interested in shaping the treatment of people suffering from a serious rare [. .. ] based on their maturity level and preferences Affinity for new technologies e. g. AI, IVA Strong commercial business acumen, strategic and innovative thinking Digital and analytical capabilities to analyze, transform data and feedback into insights li, , 2, , true, , ulli, , 1, , Normal Adhering to compliance, achieving and maintaining all applicable regulatory, legal and operational rules and procedures Strong communication skills in German English, both written and oral Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, [. .. ] leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visitand follow us on X (formerly Twitter; Blueprint Meds) and Linked In. Blueflex is our operating model which optimizes culture, productivity, flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility. Blueflex allows for [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Arizona State University
• nürnberg, BY
Führungs-/ Leitungspositionen Werkstudenten
[. .. ] Director of Student Success for Shufeldt School of Medicine and Medical Engineering provides strategic leadership and operational oversight for student services and engagement initiatives. This role will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] report to the Associate Dean of Student Affairs with Shufeldt School of Medicine and Medical Engineering and is responsible for managing the day-to-day operations of the Student Affairs office, supervising support staff, ensuring compliance with accreditation standards, assisting with budget planning and management, and overseeing student interest groups and their associated budgets. [. .. ] milestones, events, and engagement points and programming. Draft, maintain, and house cycle reporting for all Student Affairs units with the goal of gleaning insights about new or changing trends, YOY data, and progress toward strategic changes. Participate on SOMME committees, subcommittees, and workgroups. Join national and regional communities within the Association of American Medical Colleges (AAMC) and the Group on Student Affairs (GSA) to stay aware of national and regional trends in medical school, as well as to build connections and [. .. ] The John Shufeldt School of Medicine and Medical Engineering at Arizona State University, a flagship component of the broader ASU Health initiative, is boldly re-imagining medical education by merging clinical medicine, biomedical science, engineering, and technology into one integrated student experience. Built from the ground up for todays health-care challenges, the school trains physicians who not only provide exceptional patient care but also lead innovation, applying artificial intelligence, advanced diagnostics, and human-centered design to transform the future of [. .. ]
Job vor 12 Tagen bei Neuvoo.com gefunden
Jazz Pharmaceuticals
Associate Director, Head of MSL Oncology, Germany
• Munich
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree [. .. ] alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the [. .. ]
Job am 03.12.2025 bei Neuvoo.com gefunden
Jazz Pharmaceuticals
• Munich
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree [. .. ] alignment and collaboration. Execution of Medical Strategy and Scientific Excellence: Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, high-quality medical information to both internal stakeholders and external customers. Strategic Cross-Functional Collaboration and Insight Integration: Ensure delivery of the [. .. ]
Job gestern bei Neuvoo.com gefunden
Universit du Luxembourg
Full or Associate Professor (promotion track) in Bioinformatics
• Berlin
Work-Life-Balance
[. .. ] scientific level Set up and develop your own research group in the field of bioinformatics or related areas Lead impactful interdisciplinary research by reaching out to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experimental, computational and clinical research groups within the collaborative environment of the University and the LCSB Supervise and mentor graduate students and early-career researchers Secure external research funding at national and international level Foster collaborations within and outside the university Develop and deliver engaging courses at undergraduate and postgraduate levels Engage with industry, [. .. ] record proven by high level publications, conference presentations and participation in international research collaborations Proven experience in interdisciplinary research, with a focus on integrated analyses of different types of biomedical data (multi-omics, imaging, clinical data) Leading expertise in areas such as protein structure dynamics, computational genomics, or metabolic modeling Demonstrated success in securing research funding, including highly competitive international grants Proven leadership skills, including personnel and budget management skills Proven excellence in teaching and mentoring students Strong communication and interpersonal [. .. ] We encourage early application. To ensure full consideration, candidates should apply by 11.01.2026. General Information: Contract Type: Academic-Permanent. This position is offered at the Full Professor or Associate Professor level, depending on qualification. Both positions are tenured. At the Associate Professor level, promotion to Full Professor is possible after 5 years upon positive evaluation. Work Hours: Full Time 40.0 Hours per Week Planned Start Date: 01.09.2026 Location: Belval Campus Internal Title: Full professor or Chief [. .. ]
Job gestern bei Neuvoo.com gefunden
Universit du Luxembourg
• Saarland
Work-Life-Balance
[. .. ] scientific level Set up and develop your own research group in the field of bioinformatics or related areas Lead impactful interdisciplinary research by reaching out to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experimental, computational and clinical research groups within the collaborative environment of the University and the LCSB Supervise and mentor graduate students and early-career researchers Secure external research funding at national and international level Foster collaborations within and outside the university Develop and deliver engaging courses at undergraduate and postgraduate levels Engage with industry, [. .. ] record proven by high level publications, conference presentations and participation in international research collaborations Proven experience in interdisciplinary research, with a focus on integrated analyses of different types of biomedical data (multi-omics, imaging, clinical data) Leading expertise in areas such as protein structure dynamics, computational genomics, or metabolic modeling Demonstrated success in securing research funding, including highly competitive international grants Proven leadership skills, including personnel and budget management skills Proven excellence in teaching and mentoring students Strong communication and interpersonal [. .. ] We encourage early application. To ensure full consideration, candidates should apply by 11.01.2026. General Information: Contract Type: Academic-Permanent. This position is offered at the Full Professor or Associate Professor level, depending on qualification. Both positions are tenured. At the Associate Professor level, promotion to Full Professor is possible after 5 years upon positive evaluation. Work Hours: Full Time 40.0 Hours per Week Planned Start Date: 01.09.2026 Location: Belval Campus Internal Title: Full professor or Chief [. .. ]
Job gestern bei Neuvoo.com gefunden
Universit du Luxembourg
Full or Associate Professor (promotion track) in Bioinformatics
• Rhineland- Palatinate Saarburg
Work-Life-Balance
[. .. ] scientific level Set up and develop your own research group in the field of bioinformatics or related areas Lead impactful interdisciplinary research by reaching out to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experimental, computational and clinical research groups within the collaborative environment of the University and the LCSB Supervise and mentor graduate students and early-career researchers Secure external research funding at national and international level Foster collaborations within and outside the university Develop and deliver engaging courses at undergraduate and postgraduate levels Engage with industry, [. .. ] record proven by high level publications, conference presentations and participation in international research collaborations Proven experience in interdisciplinary research, with a focus on integrated analyses of different types of biomedical data (multi-omics, imaging, clinical data) Leading expertise in areas such as protein structure dynamics, computational genomics, or metabolic modeling Demonstrated success in securing research funding, including highly competitive international grants Proven leadership skills, including personnel and budget management skills Proven excellence in teaching and mentoring students Strong communication and interpersonal [. .. ] We encourage early application. To ensure full consideration, candidates should apply by 11.01.2026. General Information: Contract Type: Academic-Permanent. This position is offered at the Full Professor or Associate Professor level, depending on qualification. Both positions are tenured. At the Associate Professor level, promotion to Full Professor is possible after 5 years upon positive evaluation. Work Hours: Full Time 40.0 Hours per Week Planned Start Date: 01.09.2026 Location: Belval Campus Internal Title: Full professor or Chief [. .. ]
Job gestern bei Neuvoo.com gefunden
Universit du Luxembourg
Full or Associate Professor (promotion track) in Bioinformatics
• Rheinland- Pfalz Körperich
Work-Life-Balance
[. .. ] scientific level Set up and develop your own research group in the field of bioinformatics or related areas Lead impactful interdisciplinary research by reaching out to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experimental, computational and clinical research groups within the collaborative environment of the University and the LCSB Supervise and mentor graduate students and early-career researchers Secure external research funding at national and international level Foster collaborations within and outside the university Develop and deliver engaging courses at undergraduate and postgraduate levels Engage with industry, [. .. ] record proven by high level publications, conference presentations and participation in international research collaborations Proven experience in interdisciplinary research, with a focus on integrated analyses of different types of biomedical data (multi-omics, imaging, clinical data) Leading expertise in areas such as protein structure dynamics, computational genomics, or metabolic modeling Demonstrated success in securing research funding, including highly competitive international grants Proven leadership skills, including personnel and budget management skills Proven excellence in teaching and mentoring students Strong communication and interpersonal [. .. ] We encourage early application. To ensure full consideration, candidates should apply by 11.01.2026. General Information: Contract Type: Academic-Permanent. This position is offered at the Full Professor or Associate Professor level, depending on qualification. Both positions are tenured. At the Associate Professor level, promotion to Full Professor is possible after 5 years upon positive evaluation. Work Hours: Full Time 40.0 Hours per Week Planned Start Date: 01.09.2026 Location: Belval Campus Internal Title: Full professor or Chief [. .. ]
Job gestern bei Jobleads gefunden
Medical Science Liaison Rare Tumour-Austria (all genders)
• Wien
[. .. ] the local, regional, and national level. Serve as a scientific expert to the medical community and facilitate the appropriate exchange of scientific information. Communicate experts opinion and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] feedback on new data and clinical trends to Medical Affairs and translate this information into strategic recommendations to enhance science and advance patient care. Act as primary liaison to investigators interested in developing and performing investigatorinitiated research. Collaborate with the Clinical Operations organization to enhance patient enrollment in companysponsored clinical trials by identifying appropriate clinical trial [. .. ] empowers everyone to work their magic and champion human progress Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity Seniority level: Associate; Employment type: Fulltime; Job function: Research and Science; Industry: Pharmaceutical Manufacturing. #J-18808-Ljbffr 72699533 [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Associate Director, Head of MSL Oncology, Germany
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Reporting to the Country Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Director Germany, the Associate Director, Head of MSL Oncology is accountable for driving the Country Medical Affairs strategy and executing programs that support the successful development and commercialization of Jazz Pharmaceuticals oncology portfolio. This role includes direct leadership of the Oncology MSL team. Success in this position requires strong leadership capabilities, a high degree [. .. ] drive alignment and collaboration. Execution of Medical Strategy and Scientific Excellence Drive the effective execution of the medical strategy and associated plans. Maintain and continuously develop deep expertise in oncologyrelated clinical and scientific literature to position both yourself and the team as trusted subject matter experts. Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and collaboration. Support data generation initiatives, including the reactive evaluation of Investigator Sponsored Trial (IST) proposals. Uphold the highest standards of pharmacovigilance, compliance, and adherence to SOPs. Ensure the delivery of accurate, highquality medical information to both internal stakeholders and external customers. Strategic Cross Functional Collaboration and Insight Integration Ensure delivery of the German [. .. ]
Job am 02.12.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
Führungs-/ Leitungspositionen
Associate Medical Director/ Medical Director About Us The development of novel, effective and safe therapies for the treatment of cancer is one of the main challenges for modern medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of [. .. ] that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full lifecycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development [. .. ] consents, and other protocolrelated 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations. Demonstrated ability to establish effective scientific partnerships with key partners, experience in managing KOLs and CROs, [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Dortmund, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Stuttgart, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Essen, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Job am 04.10.2025 bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Leipzig, Sachsen
Führungs-/ Leitungspositionen
[. .. ] of helping patients world-wide. Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Your [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] mission Provide 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 and program level regulatory documents such as protocol amendments, imaging/ pathology/ DSMB charters, briefing books, BLA/ MAA, ODD, breakthrough applications etc. Act as clinical [. .. ] 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 clinical development processes such as IND, CTA and BLA/ NDA filings; good understanding of relevant FDA and EMA regulations Demonstrated ability to establish effective scientific partnerships with key partners, Experience in managing KOLs and CROs, [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Research Associate (CRA) (m/w/d) Zelltherapie (Außendienst)
• Hamburg
Clinical Research
Associate (CRA) (m/w/d) Join to apply for the Clinical Research Associate (CRA) (m/w/d) role at Astra Zeneca Innovativ, dynamisch und nachhaltig: Als eines der weltweit führenden [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Unternehmen der forschenden Arzneimittelindustrie bieten wir bei Astra Zeneca die besten Möglichkeiten für Ihre persönliche und berufliche Entwicklung. Denn für uns [. .. ] und regulatorischen Anforderungen Gutes Verständnis hinsichtlich medizinischer Fragestellungen Verständnis von unterschiedlichen Studien und Prozessanforderungen und daraus abgeleitetes Setzen der richtigen Prioritäten Erfahrung im Monitoring elektronischer Case Report Forms (Web Based Data Capture) und in der Erstellung von Monitoring Reports Selbständige, effektive, und strukturierte Organisation Fähigkeit zum analytischen und lösungsorientierten Denken Hohe Teamfähigkeit sowie der Fähigkeit, schnell auf sich ändernde Anforderungen zu reagieren Ausgeprägte Kommunikationsfähigkeit sowie sehr gute Deutsch- und Englischkenntnisse Bereitschaft zu häufigen Dienstreisen mit auswärtigen Übernachtungen Freuen Sie Sich Auf [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Site Relationship Manager
• Kassel, Hessen
Site Relationship Manager 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. This is a freelance opportunity at around 0.7 FTE. The role focuses on facilitating optimal clinical trial setup, execution and quality by understanding the local environment and building strong site relationships. Key Responsibilities Understanding the [. .. ] Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support group meetings and conferences. Collaborate with internal teams and CROs to ensure quality feasibility data and effective site selection. Provide input on sitelevel recruitment targets and strategies. Understand and support compliance with local regulatory and ethics requirements. Creating and Maintaining Strong Site Relationships Build and maintain strong relationships with site personnel to enable timely trial delivery. Conduct motivation visits to encourage engagement and recruitment. Partner [. .. ] Qualifications Bachelors or Masters degree in Life Sciences. Minimum 7 years of experience in the pharmaceutical or clinical research industry. At least 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Director, Regulatory Affairs CMC Europe
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Führungs-/ Leitungspositionen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] and/or interns. Develop and implement regulatory operating guidelines and common work practices/ strategies within the team. Qualifications 1012 years of related work experience (Director candidates typically bring 12 years; Associate level candidates may be considered with 10 years and strong potential) , including 8 years in Regulatory Affairs CMC in the biotech/ pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus. Proven experience serving as a primary RACMC contact to health [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical data associate pro Jahr?
Als Clinical data associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 212 offene Stellenanzeigen für Clinical Data Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Associate Jobs?
Aktuell suchen 21 Unternehmen nach Bewerbern für Clinical Data Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Associate Stellenangebote:
- Astra Zeneca (19 Jobs)
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- Medpace (11 Jobs)
- TFS Health Science (10 Jobs)
- IQVIA (6 Jobs)
In welchen Bundesländern werden die meisten Clinical Data Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Associate Jobs werden derzeit in Bayern (25 Jobs), Nordrhein-Westfalen (23 Jobs) und Niedersachsen (21 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Associate Jobs?
Clinical Data Associate Jobs gehören zum Berufsfeld Medizintechnik.
