46 Jobs für Clinical Data Analyst
Stellenangebote Clinical Data Analyst Jobs
Job vor 3 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
• AT- 9 Wien
Homeoffice möglich
[. .. ] is responsible for the timely submission of applications to health authorities. We also work closely with the Submission Management Group (SMG) in Pharma Technical Regulatory (PTR) as [...]
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[...] a document and data hub for Quality documents. The Clinical Trial Regulatory Management Team enables the development of organizational and people capabilities of the future, we support and optimize the delivery of projects and initiatives to the organization both on the molecule and moleculeenabling portfolio. Global Labeling ensures the consistent and safe use of our medicines through highquality labels to [. .. ] to interface effectively with submission leads and colleagues located in other countries. Ability to work in fastpaced global teams Fluent in written and spoken English Logical thinking and/or process analyst mentality In exchange we provide you with Development opportunities: Roche is rich in learning resources. We provide constant development opportunities, free language courses trainings, the possibility of international assignments, internal position changes and the chance to shape your own career. Excellent benefits flexibility: competitive salary and cafeteria package, annual bonus, [. .. ]
Job vor 9 Tagen bei Mindmatch.ai gefunden
Roche
Senior Product Owner (m/f/d)
• AT- 9 Wien
Homeoffice möglich
[. .. ] product team and the central decision-maker on product scope and priorities. Operating within Scaled Agile Framework (SAFe) , you will work cross-functionally with software engineering, design, medical, [...]
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[...] regulatory, data privacy, and commercial teams to shape digital solutions that deliver measurable impact for users and the business. Key responsibilities Product Definition Backlog Ownership Define and deliver product value : Understand the strategic vision and desired outcomes of my Sugr, and translate them into actionable features and user stories Lead the product definition in collaboration with the scrum master and development team (UI/ UX team, architecture, engineering, business analyst) including other relevant inputs that may affect the scope of the product (medical affairs, data security, data privacy and legal) Ensure quality and compliance : Approve product increments based on the Definition of Done, and ensure features meet both functional and nonfunctional requirements (performance, privacy, security, etc. ) Agile Delivery [. .. ] the standard of care for humankind. Our culture inspires us to create healthcare that is sustainable, efficient and financially viable. Healthcare that is built on peoples needs, strong data and clinical insights. Healthcare that saves lives. Interested? Great. Wed like to hear from you Just click that Apply Now button and send us your CV in English and anything else that you think might impress us. Roche is an Equal Opportunity Employer. J-18808-Ljbffr 70521240 [. .. ]
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 to accelerate [...]
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[...] 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 [. .. ] 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 [. .. ] monitoring, and collaborate with site teams to implement effective quality monitoring processes that support successful clinical trials. Employment Details Seniority level: Mid Senior level Employment type: Fulltime Job function: Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x. Get notified about new Clinical Research Associate jobs in Vienna, Vienna, Austria. EEO Statement The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist [. .. ]
Job am 14.11.2025 bei Mindmatch.ai gefunden
Medtronic plc
Senior Reimbursement Analyst (m/f/d) - EMEA
• AT- 9 Wien
Senior Reimbursement
Analyst (m/f/d) - EMEA page is loaded # # Senior Reimbursement Analyst (m/f/d) - EME Aremote type: Remotelocations: Mollsfeld, Meerbusch, Germany: Vienna, Vienna, Austriatime type: Full timeposted on: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Posted Todayjob requisition id: R51188At Medtronic you can begin a life-long career of exploration and innovation, while helping [. .. ] include the following and other duties may be assigned: In this role you will carry out the responsibilities within the framework of contribution to multi-disciplinary teams including outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support in HTAs and funding submissions within EMEA, with particular focus to but not limited to the DACH region. Execute health economic (HE) [. .. ]
Job am 14.10.2025 bei Mindmatch.ai gefunden
Syneos Health
• 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 [...]
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[...] 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) [. .. ] processes within area of responsibility. Requires practical knowledge of a professional area, typically obtained through education combined with experience. Seniority level Entry level Employment type Full-time Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x Get notified about new Clinical Research Associate jobs in Vienna, Vienna, Austria. CRA I or CRA II (m/w/d) , Single Sponsor, home-based Austria Were unlocking community knowledge in a new way. Experts add [. .. ]
Job am 08.10.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Amyloidosis, North-Eastern Germany (Rostock, Berlin, Leipzig, . . .
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
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[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. This Is What You Will Do The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports [. .. ] between expert KOLs and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data [. .. ] recruitment) , as well as work authorization and employment eligibility verification requirements. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Alexion Pharmaceuticals, Inc. by 2x Get notified about new Medical Science Liaison jobs in Munich, Bavaria, Germany. Scientific Affairs Manager-Germany (Southwest) Medical Affairs Manager Germany and Austria (f/m/d) Associate Director Medical Affairs (MSL Lead) Senior Manager (m/[. .. ]
Job gestern bei Jobleads gefunden
• Nordrhein- Westfalen
[. .. ] Key Responsibilities Develop and maintain peer-to-peer collaborations and relationships with key medical experts in the ophthalmology community. Support medical affairs (e. g. , scientific exchange, conference support) [...]
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[...] and clinical development initiatives (e. g. , site identification, trial recruitment) . Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training. Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders. Support the medical community with up-to-date medical information, robust disease expertise, and product information. Communicate clinical insights on new data to Apellis Medical Affairs and to inform medical strategy for the therapeutic area. Train internal stakeholders on key scientific and medical topics in relevant therapeutic area. Develop an understanding of the regional landscape including specialties involved in care of patients. Maintain effective and appropriate communication among internal stakeholders while maintaining [. .. ] the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 71600614 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Group Leader-Cancer Research (m/f/d) - Deutsches Krebsforschungszentrum (DKFZ)
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Jobticket
[. .. ] the scientific community at the campus and the DKTK partner site. Mentor junior scientists and students. Engage in teaching and academic training activities (optional) . Qualifications Ph [...]
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[...] D in life or data sciences and/or MD in medicine. Excellent postdoctoral achievements (typically 36 years) in a research area that aligns with the focus area. Significant international research experience (typically 3 years) . Proven expertise in translational cancer research, ideally bridging preclinical and clinical approaches. Strong publication record and history of ambitious acquisition of competitive thirdparty funding, appropriate to career stage. Leadership skills, diversity competency, and commitment to mentoring junior scientists and students. Vision for an innovative, internationally competitive research program. Strong motivation to collaborate with other DKTK sites and within interdisciplinary networks. Experience [. .. ] programs. Sustainable travel to work: subsidised Germany job ticket. Corporate Health Management Programme offering a holistic approach to wellbeing. Seniority level Mid Senior level Employment type Parttime Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at DKFZ German Cancer Research Center by 2x. Get notified about new Lead Researcher jobs in Mainz, Rhineland Palatinate, Germany. #J-18808-Ljbffr 71360606 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
[. .. ] are launching new in-home and virtual services to improve access, close care gaps, and manage chronic conditions. About the Role We are looking for a highly motivated [...]
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[...] Senior Product Analyst to support our growing product team. This role will partner closely with our product managers and cross-functional leaders to accelerate product development, support team operations, and drive forward strategic initiatives that shape the future of in-home care. As a Senior Product Analyst, you will be a force multiplier [. .. ] and crossteam communication artifacts. Product Development and Execution Work with Product Managers across different visit offerings to support requirement documentation, user research, backlog organization, and MVP delivery. Analyze operational and clinical data to identify areas for improvement or product iteration. Support endtoend product lifecyclefrom discovery and business case development to launch tracking and retrospective reviews. Research and Analysis Conduct qualitative and quantitative research to evaluate new product opportunities, care models, and market trends. Support value proposition development by analyzing member, provider, and [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Senior Analyst, Project Management
[. .. ] Summary Primary Job Duties Responsibilities Implements a comprehensive configuration management plan that outlines the strategy, policies, procedures, and guidelines for managing the organizations hardware, software, and documentation. [...]
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[...] Analyzes complex configuration data to provide insights into configuration management metrics, trends, and compliance issues. Applies in-depth knowledge of configuration management tools and systems to support organizational operations. Codes and/or writes custom configurations or extensions to tailor technology functions to the specific needs of the organization. Communicates with project managers, developers, and [. .. ] align with relevant industry standards, regulations, and security requirements. Required Qualifications 1 year minimum of claims processing experience Experience with system testing and post golive validation QNXT Experience Familiarity with clinical and code editing concepts and products (Example: Claims Xten, Cotiviti PPM CV) Extensive knowledge of CPT, HCPCS, ICD-10 coding Preferred Qualifications Prior Relevant Work Experience 3-5 years Working knowledge of problem solving and decision making skills Certified Information Systems Security Professional (CISSP) preferred. Certified Analytics Professional (CAP) preferred. [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Berlin
[. .. ] Bayers Cardiovascular, Renal and Inflammation (CVRI) research area and play a key leadership role in advancing our kidney disease portfolio. You will lead in vitro pharmacology initiatives [...]
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[...] from concept to clinical translation, drive scientific innovation, and guide cross-functional teams to develop transformative therapies for patients worldwide. Your Tasks And Responsibilities You will drive the development of a sustainable renal disease research portfolio within Bayers CVRI organization You will hold full accountability for in vitro pharmacology across project teams, providing strategic [. .. ] (e. g. flow cytometry, microscopy, imaging) , functional cellular assay development, and molecular biology You demonstrate strong leadership and collaboration skills within project teams or matrix environments You communicate complex data effectively across functions and maintain strong partnerships with internal and external stakeholders You are fluent in English, both spoken and written; German skills are an advantage WHAT WE OFFER Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us We ensure [. .. ] We are committed to treating all applicants fairly and avoiding discrimination. Location: Berlin Division: Pharmaceuticals Reference Code: 856503 Seniority level: Mid-Senior level Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Chemical Manufacturing, Pharmaceutical Manufacturing, Biotechnology Research Referrals increase your chances of interviewing at Bayer by 2x. Get notified about new Principal Scientist jobs in Berlin, Berlin, Germany. #J-18808-Ljbffr 70584926 [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Senior Product Owner (m/f/d)
• Wien
Homeoffice möglich
[. .. ] product team and the central decision-maker on product scope and priorities. Operating within Scaled Agile Framework (SAFe) , you will work cross-functionally with software engineering, design, medical, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory, data privacy, and commercial teams to shape digital solutions that deliver measurable impact for users and the business. Key responsibilities Product Definition Backlog Ownership Define and deliver product value : Understand the strategic vision and desired outcomes of my Sugr, and translate them into actionable features and user stories Lead the product definition in collaboration with the scrum master and development team (UI/ UX team, architecture, engineering, business analyst) including other relevant inputs that may affect the scope of the product (medical affairs, data security, data privacy and legal) Ensure quality and compliance : Approve product increments based on the Definition of Done, and ensure features meet both functional and nonfunctional requirements (performance, privacy, security, etc. ) Agile Delivery [. .. ] the standard of care for humankind. Our culture inspires us to create healthcare that is sustainable, efficient and financially viable. Healthcare that is built on peoples needs, strong data and clinical insights. Healthcare that saves lives. Interested? Great. Wed like to hear from you Just click that Apply Now button and send us your CV in English and anything else that you think might impress us. Roche is an Equal Opportunity Employer. #J-18808-Ljbffr 70585224 [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Schweinheim, Nordrhein- Westfalen
[. .. ] and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The position as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Reimbursement Analyst (m/f/d) is an exciting opportunity to work with Medtronics Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our [. .. ] include the following and other duties may be assigned : In this role you will carry out the responsibilities within the framework of contribution to multidisciplinary teams including outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support in HTAs and funding submissions within EMEA, with particular focus to but not limited to the DACH region. Execute health economic (HE) [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
Clinical Study Analyst (m/f/d)
• Heidelberg, Baden- Württemberg
Jobticket
Your tasks Lead GCP Compliant
Clinical Diagnostic Studies: Design, implement, and manage diagnostic accuracy studies in compliance with ICHGCP and regulatory standards, ensuring
data integrity, patient safety, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ethical conduct. Project Management Excellence: Plan, allocate resources, schedule, and oversee all aspects of the project, including protocol development, ethics approvals, study site management, and data collection, to ensure timely and highquality execution. Data Oversight, Analysis and Scientific Contribution: Build research networks, analyze clinical and diagnostic [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Meerbusch, Nordrhein- Westfalen
Senior Reimbursement
Analyst (m/f/d) - EMEA Medtronic Meerbusch, North Rhine-Westphalia, Germany At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and [...]
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[...] equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day [. .. ] the open position. Only for Austrian applicants: Yearly targeted salary starting from 60, 000.00 with willingness for market-based overpayment depending on professional qualification and experience. Responsibilities Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support in HTAs and funding submissions within EMEA, with particular focus to but not limited to the DACH region. Execute health economic (HE) [. .. ] effectiveness, budget impact, and cost-of-illness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossiers for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Experienced Informatics Analyst
We are currently seeking an experienced informaticist to join our Informatics team who will lead advanced analyses of methodological
data to inform study design decisions. The Informatics team utilizes [...]
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[...] informatics principles and techniques to architect, mine, analyze, and visualize clinical trial data to inform study design choices for pharmaceutical development. The informaticist will create predictive data models to identify and analyze patterns, then program compelling visualizations of the data to support feasibility strategies. The team is seeking an experienced candidate for a senior-level position to contribute new skills to our team, support team growth, and foster fellow analyst development. The Informatics Team is a highly collaborative team with members in both the Cincinnati and London offices. This team supports clinical operation, medical, and feasibility teams with advanced data query and analysis. The Informatics Team also works side-by-side business analytics and software engineering to architecture innovative data [. .. ]
Job am 15.11.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Join to apply for the Trade Compliance
Analyst II role at Beckman Coulter Diagnostics Are you ready to accelerate your potential and make a real difference within life sciences, [...]
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[...] diagnostics and biotechnology? At Beckman Coulter Diagnostics, one of Danahers 15+ operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact. [. .. ] you and your unique viewpoint matter. By harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, [. .. ] operational efficiency and compliance. Coordinate and prepare export license applications and permits, including enduser screenings, Letters of Indemnity, and submissions to authorities such as BAFA, CITES, and USDA. Manage trade data classification, country of origin, valuation, and recordkeeping to ensure accurate and timely customs clearance in accordance with applicable regulations. Conduct postentry reviews, selftesting audits, and support government audit activities as required. Support Daily Management, KPI reporting, and continuous improvement initiatives, contributing to standard work development and DBS maturity. Essential Requirements [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Wien
Senior Reimbursement
Analyst (m/f/d) - EMEA page is loaded # # Senior Reimbursement Analyst (m/f/d) - EME Aremote type: Remotelocations: Mollsfeld, Meerbusch, Germany: Vienna, Vienna, Austriatime type: Full timeposted [...]
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[...] on: Posted Todayjob requisition id: R51188At Medtronic you can begin a life-long career of exploration and innovation, while helping [. .. ] may include the following and other duties may be assigned:In this role you will carry out the responsibilities within the framework of contribution to multi-disciplinary teams including outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support in HTAs and funding submissions within EMEA, with particular focus to but not limited to the DACH region. Execute health economic (HE) [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
[. .. ] millions of lives and are ready to change millions more. This position is focused on medical affairs activities in the region, bridging the company with healthcare professionals [...]
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[...] (HCPs) and supporting clinical strategy, product development and educational activities. Position Summary The Field Medical Science Specialist/ Medical Affairs Specialist acts as the bridge between the company and healthcare professionals (HCPs) , providing in-depth scientific knowledge, practical medical applications and support for our products and research. The FSS is the medical and scientific expert in the field responsible for engaging with key opinion leaders (KOLs) , facilitating in-depth discussions on the benefits and use of CGM for patients with diabetes, including clinical data and its optimal use. Your insights will drive our clinical strategy, support product development and enhance our educational activities. Key Responsibilities Scientific Engagement and Advocacy: Serve as subject matter expert on Dexcom devices and facilitate scientific discussions, presentations and educational activities to communicate clinical value and application. Establish and maintain [. .. ] employees, or any other part of the company. Dexcom is not responsible for fees related to unsolicited resumes/ applications. Seniority level Not Applicable Employment type Full-time Job function Research, Analyst, and Information Technology Industries Medical Equipment Manufacturing Referrals increase your chances of interviewing at Dexcom by 2x Sign in to set job alerts for Medical Affairs Specialist roles. #J-18808-Ljbffr 69376270 [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Clinical Trial Manager-50 office-based
• München, Bayern
Clinical Trial Manager-50 office-based Join to apply for the Clinical Trial Manager-50 office-based role at Syneos Health. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to [...]
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[...] accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market [. .. ] where everyone feels like they belong. Job Responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the [. .. ] adapts new procedures, techniques, tools, etc. understands basic management approaches such as work scheduling, prioritizing, coaching and process execution. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 69120788 [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Validation Analyst (f/m/x)
• Estenfeld (VGem) , Bayern Estenfeld (VGem)
Jobticket Work-Life-Balance
We are looking for you as Validation
Analyst (f/m/x) in full time (40h/ week) at our Estenfeld (near Würzburg) site. Be a part of driving
clinical trials faster [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with your daily performance. You will be responsible for ensuring that our customers (pharma companies) can be confident that our test devices for our Precision Motion, Respiratory and Cardiac business lines are working as intended. What We Offer Hybrid work environment (3 days in office, 2 days remote) [. .. ] parking We have both social and wellness committees that organize parties, events and activities What Youll Be Doing Write concise and complete documentation to support the validation for internal clinical data systems or third party vendor systems. Documentation would include but is not limited to: Test Strategies, Test Reports, Test Summary Reports, Deviations and Traceability Evaluate new and updated systems or configurations to determine the necessary validation steps to assure compliance of those systems or configurations with industry standards and regulatory [. .. ]
Job am 05.11.2025 bei Jobleads gefunden
Sr/ Pr Biostatistician (Europe-Oncology )
• München, Bayern
[. .. ] to apply for the Sr/ Pr Biostatistician (Europe-Oncology) role at Syneos Health. Syneos Health is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] by translating clinical, medical affairs, and commercial insights into outcomes that address modern market realities. About the Role The Sr/ Pr Biostatistician will provide statistical support throughout the lifecycle of clinical projects, collaborating with sponsors and cross-functional teams to ensure high-quality, regulatorycompliant analyses. Responsibilities Provides support across all assigned statistical tasks [. .. ] specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs) , database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. Conducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications. Implements company objectives and creates alternative solutions to address business [. .. ] of the EU Equality Directive and the Americans with Disabilities Act. Summary Previous lead experience within Oncology is required. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 68477227 [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
Director Scientific/ Medical Writing
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] for the Director Scientific/ Medical Writing role at Bio NTech SE. Mainz, Germany; London, United Kingdom Full time Job ID: 9928 Seniority Level Director Employment Type Full-time [...]
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[...] Job Function Research, Analyst, and Information Technology Key Responsibilities Write, edit, and format a wide range of documents (of low to high complexity) required for research, nonclinical, clinical development, and postapproval life cycle management largely according to standard procedures. Coordinate the document preparation, review, and approval. Check and revise documents with regard to scientific content, completeness, consistency, and standards compliance. Manage outsourced tasks: plan, support So W set up, coordinate, and manage external writers providing medical writing services. Coordinate [. .. ] Annual Reports, RMPs, RFI response documents, diversity plans, PIPs/ PSPs, and other CTD Module1 documents. Prior experience editing/ reviewing R D reports. Prior experience drafting R D reports from source data, covering low to high complexity variants. Prior experience as a line manager/ with line management tasks. Knowledge of basic business acumen (planning, operations, finance, and strategy) . Knowledge of budget, resource, and project management. Additional Skills or Knowledge A can do attitude with the ability to work according to tight [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
Senior Manager Biostatistics R D (m/f/x)
• München, Bayern
[. .. ] Our European headquarters are in Munich, Germany, with affiliates in 15 European countries and Canada. Role Purpose We are seeking a Senior Biostatistician to support oncology development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] within an international clinical development team. Reporting to the Director of Biostatistics, you will lead complex study design and statistical analysis efforts, collaborating closely with crossfunctional teams and external partners such as contract research organizations (CROs) . Roles and Responsibilities Lead statistical activities for complex oncology studies, including study design, protocol development, case report form review, statistical analysis plan development, data analysis, and clinical study report contributions. Serve as the primary statistical contact for assigned studies, providing expert guidance to study teams and ensuring highquality data in collaboration with data managers. Provide input into drug development plans to ensure scientifically sound study designs that meet regulatory requirements and target product profiles. [. .. ] CV Further qualification documents What We Offer Excellent benefits Worklife balance Growth and development opportunities Health and wellbeing support Seniority Level Mid Senior level Employment Type Fulltime Job Function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 67587429 [. .. ]
Job am 29.10.2025 bei Jobleads gefunden
Scientific Affairs Manager-Germany (Southwest)
• München, Bayern
[. .. ] internal colleagues. He/ she will support the local Hospital Affairs Lead (HAL) and will be responsible for building peer to peer relationships with external experts and other [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stakeholders to provide clinical, scientific, and medical education in the territory. The SAM will support research initiatives, advisory boards, and other compliant scientific exchange activities to support Rhythms strategically aligned Medical Affairs Plan aimed at identifying and addressing the unmet needs of people living with rare genetic disorders of obesity. Responsibilities And Duties Responsible [. .. ] clinical trials and investigators to drive trial enrolment. Develop and implement a novel scientific communication plan for setmelanotide, and contribute to the medical/ scientific review of manuscripts. Interpret key scientific data and translate this information to meet educational and research needs in alignment with Rhythm Medical Communication. Provide medical/ scientific review of scientific communication platforms, medical information resources, medical education materials marketing materials to ensure local Germany compliance. Provide input and feedback on training initiatives directed at medical colleagues to deepen [. .. ] tackle tough challenges and have the courage to ask bold questions. We are eager to learn and adapt. Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 67447514 [. .. ]
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Wieviel verdient man als Clinical Data Analyst pro Jahr?
Als Clinical Data Analyst verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Analyst Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 46 offene Stellenanzeigen für Clinical Data Analyst Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Analyst Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Clinical Data Analyst Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Analyst Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Analyst Stellenangebote:
- Syneos Health (2 Jobs)
- F. Hoffmann- La Roche Gruppe (1 Job)
- Roche (1 Job)
- Medtronic plc (1 Job)
In welchen Bundesländern werden die meisten Clinical Data Analyst Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Analyst Jobs werden derzeit in Bayern (12 Jobs), Berlin (7 Jobs) und Nordrhein-Westfalen (6 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Analyst Jobs?
Clinical Data Analyst Jobs gehören zum Berufsfeld Pharmazie.
