199 Jobs für Clinical Data Associate
Stellenangebote Clinical Data Associate Jobs
Job gestern 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 Neuvoo.com gefunden
Jazz Pharmaceuticals
Associate Director, Head of MSL Oncology, Germany
• Munich Muenchen
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 vor 3 Tagen bei JobMESH gefunden
Jazz Pharmaceuticals
• Bavorsko Mnichov
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 vor 2 Tagen bei Mindmatch.ai gefunden
ICON
Clinical Research Associate (CRA) - Austria
• AT- 9 Wien
Work-Life-Balance
CRA. Austria ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Merck Healthcare
• AT- 9 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 71431710 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
Remote CRA II Home-Based in Sydney/ Melbourne
• AT- 8 Gemeinde Au
Work-Life-Balance
A leading
clinical research organization is looking for an experienced Clinical Research
Associate based in Austria to conduct and oversee clinical trials. Responsibilities include conducting site visits, ensuring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance and data integrity, and collaborating effectively with staff. Candidates should possess a Bachelors degree in a related field and at least 2 years of experience, with travel required. A competitive salary and benefits package tailored for work-life balance is offered. J-18808-Ljbffr 71412751 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
• AT- 8 Gemeinde Au
CRA II, Home-based in Sydney or Melbourne Join a global FSP partnership ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As an experienced Clinical Research Associate, you will be joining the worlds largest most comprehensive clinical research organization, powered by healthcare intelligence. You will be working alongside a world-leading pharmaceutical company. This 22year partnership is focused on leveraging cuttingedge science to make a positive impact in the therapeutic areas of cancer, cardiometabolic, vaccines, and oncology, [. .. ] make a difference, this could be the career destination for you. What you will be doing Conducting site qualification, initiation, monitoring, and closeout visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain highquality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelors degree [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
Senior CRA
• AT- 8 Gemeinde Au
[. .. ] are interested in managing the whole life cycle of the study from site selection to closeout, we want to hear from you. ICON plc is a worldleading [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking an experienced Clinical Research Associate II or Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials of a single client by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. In this FSP program you will be working on cuttingedge Oncology trials and can take ownership of the full site management lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
• AT- 8 Gemeinde Au
Führungs-/ Leitungspositionen
A leading
clinical research organization is seeking a Senior Clinical Research
Associate to oversee clinical trial activities, ensuring compliance and
data integrity. The ideal candidate will have [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an advanced degree and extensive experience as a CRA, with excellent communication and problem-solving skills. This role involves site management of oncology trials and requires the ability to travel up to 60. A competitive salary and benefits are offered, including various health insurance [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
Senior Clinical Research Associate Remote (Sydney)
• AT- 8 Gemeinde Au
A leading
clinical research organization in Austria is seeking a Clinical Research
Associate/ Senior Clinical Research Associate to manage clinical trials and ensure compliance. The ideal candidate will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] have a Bachelors degree in a relevant field and at least 2 years of experience. Responsibilities include site visits and data analysis to support innovative treatments. A competitive salary and various benefits are offered, promoting a diverse workplace culture. J-18808-Ljbffr 70914060 [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
ICON Strategic Solutions
• AT- 8 Gemeinde Au
Clinical Research
Associate/ Senior Clinical Research Associate Sydney Home based ICON plc is a worldleading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking [. .. ] Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save peoples lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Takeda
Associate Director, API Process Engineering
• AT- 9 Wien
Führungs-/ Leitungspositionen
About the role As
Associate Director, API Process Engineering, you will be Takedas global expert for smallmolecule API manufacturing processes across batch and continuous platforms. You will apply chemical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engineering and process chemistry fundamentals to design, scale, and control API processes from clinical development through commercial supply. Through the integration of mechanistic modelling, process simulation, and rigorous data analysis you will deepen process understanding, strengthen control strategies, and support regulatory submissions for global markets. You will become the central hub for API process knowledge, driving best practices and continuous improvement across Takedas manufacturing network and external CMOs. How you will contribute Lead the Small Molecules API Manufacturing Sciences [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Takeda
• AT- 4 Linz
Führungs-/ Leitungspositionen
About the role As
Associate Director, API Process Engineering, you will be Takedas global expert for smallmolecule API manufacturing processes across batch and continuous platforms. You will apply chemical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engineering and process chemistry fundamentals to design, scale, and control API processes from clinical development through commercial supply. Through the integration of mechanistic modelling, process simulation, and rigorous data analysis you will deepen process understanding, strengthen control strategies, and support regulatory submissions for global markets. You will become the central hub for API process knowledge, driving best practices and continuous improvement across Takedas manufacturing network and external CMOs. How you will contribute Lead the Small Molecules API Manufacturing Sciences [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
bio Mrieux
Medical Scientific Liaison (MSL) for Austria and Switzerland (m/f/d)
• AT- 9 Wien
[. .. ] evidence generation by participating in company-sponsored postmarket studies, supporting Investigator Initiated Trials (IITs) in line with global strategy and according to Medtech requirements and bio Mrieux SOPs, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supporting clinical development initiatives including site identification, trial recruitment, registry and presentation of final approved data. Provide operational and medical support to marketing and sales teams (Account Managers, Clinical Education Managers, Business Developers) . Qualifications Academic degree in Medicine or Pharmacology. Advanced scientific degree (MD, Ph D, Pharm D) with relevant industry experience is desirable. Experience in the therapy area of infectious disease or intensive care is strongly [. .. ] Flexible working time models tailored to your individual needs, mobile working and a partial pension scheme. Attractive social benefits package. Stateoftheart work environment and digital equipment. Job details Seniority level: Associate. Employment type: Fulltime. Job function: Sales, Health Care Provider, and Project Management. Industries: Pharmaceutical Manufacturing, Medical Equipment Manufacturing, Hospitals and Health Care. We look forward to receiving your application J-18808-Ljbffr 70402507 [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Blueprint Medicines, a Sanofi company
• AT- 9 Wien
Homeoffice möglich
Location (s) : Vienna Austria Level of position:
Associate Director Position type: 60 field-based 40 home-office based; Temporary Reporting Line: This role reports to the Director of International Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs How will your role help us transform hope into reality The Field Medical Advisor role at Blueprint Medicines Alpine is a critical position within the organization responsible [. .. ] role in driving the success of Blueprints mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a reliable bridge between clinical research market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Field Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas new innovations and new ways of [. .. ] non-Interventional clinical trials in close collaboration with with Clinical development Clinical Operations and Global Medical Affairs teams. Ensures a strategic approach to such programs and the development of clinical data to support the appropriate use of the Companys products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in the international region to ensure consistency of clinical programs from a medical perspective. Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps [. .. ]
Job vor 14 Tagen bei Mindmatch.ai gefunden
Medtronic plc
Clinical Specialist Surgical Robotics (m/w/d) - DACH
• AT- 9 Wien
Clinical Specialist Surgical Robotics (m/w/d) - DACH page is loaded # # Clinical Specialist Surgical Robotics (m/w/d) - DAC Hremote type: Remotelocations: Vienna, Vienna, Austriatime type: Full timeposted on: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Posted 6 Days Agojob requisition id: R49645At Medtronic you can begin a life-long career of exploration and [. .. ] daily healthcare delivery. The Surgical Robotics Utilization Team plays a key role in supporting the successful installation, start-up, and integration of the Hugo Surgical Robot in hospitals. As an Associate Start Up Specialist, you will work alongside experienced professionals to help ensure smooth adoption of this innovative technology by assisting with system setup, user training, and operational support. This role is designed for ambitious individuals looking to kick-start their careers in medical technology, healthcare operations, and surgical support. You [. .. ] Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls. Insight-driven care. Fresh viewpoints. Cutting-edge AI, data, and automation. Youre shaping the future of healthcare technology and defining the next generation of breakthroughs in care It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Experienced CRA Austria Syneos Health Application open. Position sought for Experienced
Clinical Research
Associate in Austria. Description Syneos Health is a leading fully integrated biopharmaceutical solutions organization built [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of everything we [. .. ] site performance and provide recommendations, communicate/ escalate serious issues, and develop action plans. Verify informed consent procedures are performed and documented for each subject, protecting confidentiality and assessing safety and data integrity at investigator sites. Based on the Clinical Monitoring/ Site Management Plan, assess site processes, conduct source document review, verify CRF data accuracy, resolve queries remotely or onsite, support data capture and electronic data capture compliance. Perform IP inventory, reconciliation, storage and security review, and confirm correct dispensing and administration [. .. ]
Job am 17.11.2025 bei Mindmatch.ai gefunden
i- Pharm Consulting
Clinical Research Associate
• AT- 9 Wien
Work-Life-Balance
Job Title:
Clinical Research
Associate (CRA) 0.8 FTE Location: Austria Duration: 12-Month Contract Travel: 6080 About the Company Join a leading global contract research organization (CRO) that partners [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with pharmaceutical, biotechnology, and medical device companies to advance innovative therapies. The organization is known for its commitment to high-quality clinical research and supports [. .. ] FTE position with significant travel (6080) . Key Responsibilities Conduct site visits to monitor clinical trial progress, protocol adherence, and regulatory compliance. Manage and maintain essential trial documentation to ensure data integrity and audit readiness. Represent the organization in the global clinical research community and maintain collaborative relationships with sites and client personnel. Assist project or clinical team managers on assigned projects and take a lead role when required. Evaluate medical research data and ensure high-quality reporting. Requirements University degree [. .. ]
Job am 08.11.2025 bei Mindmatch.ai gefunden
Healthcare Businesswomens Association
• AT- 7 Schaftenau
Führungs-/ Leitungspositionen
Job Description Summary LOCATION: Schaftenau, Austria ROLE TYPE: Hybrid Working, #LI-Hybrid Become part of our upstream process development team as
Associate Director Science Technology. In this pivotal role, youll [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] translate strategy, drive innovation and enable development as well as seamless transfer of late-phase Upstream Processing (USP) processes to our manufacturing sites. If youre passionate about science, leadership, and making a difference, this is your opportunity. Job Description We are seeking [. .. ] USP Development is a senior scientific leadership role within Drug Substance Development, responsible for driving innovation, scientific excellence and operational readiness in mammalian cell culture process development for late-phase clinical and commercial manufacturing. This position combines strategic leadership, scientific excellence and project support to ensure robust upstream processes and successful technology transfer to our manufacturing sites. Your responsibilities Strategic Leadership Shape and execute the departments strategic vision, including technology roadmaps and process optimization initiatives. Lead workstreams and contribute to global or local initiatives, such as global guidelines, development manuals or industry consortia. Champion major innovations, including the integration of modeling and simulation into late-phase development, implementation of Data Digital (D D) initiatives, and evolution of hybrid development concepts. Partner effectively across global USP networks and with key functions such as Scientific Office, Downstream Processing (DSP) , Analytical Development, Manufacturing Science Technology (MS T) , Novartis Operations, and Regulatory Affairs. Scientific Excellence Capability Building Promote knowledge exchange locally and [. .. ]
Job am 02.11.2025 bei Mindmatch.ai gefunden
IQVIA Argentina
CRA I or CRA II (m/w/d) , Single Sponsor, home-based Austria
• AT- 9 Wien
Homeoffice möglich
Join IQVIA as a
Clinical Research
Associate I or II (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. Youll enjoy [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether youre just starting out or [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Collaborating with experts at study sites and with client representatives Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices) Mentoring of less experienced team members, support as subject matter expert for specific topics [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
CRA Austria
• AT- 9 Wien
2 days ago Be among the first 25 applicants Description CRA Austria Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 24.08.2025 bei Mindmatch.ai gefunden
Bristol Myers Squibb
Therapeutic Area Specialist, Oncology (m/w/d) - Westösterreich (Salzburg, Tirol, Vorarlberg)
• AT- 9 Wien
[. .. ] ability to think strategically, drive performance, foster customer relationships and build alignment positive working relationships through a strong cross-functional collaboration. Good scientific understanding with the ability to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] simplify complex clinical data to concise and convincing messages Solution-oriented can-do mentality and ability to work effectively in complex, rapidly changing environment Open to new technologies and digital ways of working Good organizational skills, along with the ability to work on multiple tasks, and to effectively prioritize Strong motivation to continuously learn [. .. ] / careers. bms. com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Seniority level Seniority level Associate Employment type Employment type Full-time Job function Job function Sales and Business Development Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Bristol Myers Squibb by 2x Sign in to set job alerts for Therapeutic Specialist roles. Were unlocking community knowledge in a new way. Experts add insights [. .. ]
Job vor 4 Tagen 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
Associate Medical Director/ Medical Director
• 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, [. .. ]
1 von 8Weiter » Weitere Suchergebnisse laden »
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 199 offene Stellenanzeigen für Clinical Data Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Associate Jobs?
Aktuell suchen 24 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 (15 Jobs)
- Planet Pharma (11 Jobs)
- Tubulis GmbH (11 Jobs)
- Medpace (9 Jobs)
- ICON Strategic Solutions (6 Jobs)
- IQVIA (5 Jobs)
In welchen Bundesländern werden die meisten Clinical Data Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Associate Jobs werden derzeit in Bayern (21 Jobs), Nordrhein-Westfalen (17 Jobs) und Niedersachsen (16 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Associate Jobs?
Clinical Data Associate Jobs gehören zum Berufsfeld Medizintechnik.
