25 Jobs für Clinical Trials Analyst
Stellenangebote Clinical Trials Analyst Jobs
Job gestern bei Mindmatch.ai gefunden
Novocure
• AT- 9 Wien
[. .. ] patients treated with Tumor Treating Fields (TT Fields) . Additional responsibilities includebut are not limited toacting as a scientific interface between the company and HCP communities regarding [...]
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[...] communication about Novocures clinical development plans as well as other research and development activities. Developing appropriate training materials, supporting external research projects related to marketed or investigational Novocure indications, and participating in field-based activities to advance existing products and introduce new indications are also part of the role. The MSL plays an important [. .. ] therapy awareness among prescribers and nonprescribers Manage the entire Austrian territory and all associated field activities Deliver medical training on Novocure products and disease areas Support and accompany investigator Sponsored Trials (ISTs) and other research projects Provide HCP insights and market information to the company Participate in medical (Europewide) congresses, and organize and follow up on advisory boards Promote scientific advancement related to TT Fields Support Phase 3 studies in collaboration with clinical teams and researchers Build and maintain relationships with [. .. ] minimum salary is 3, 682 gross per month. However, we are willing to offer a significantly higher salary. Seniority level Mid Senior level Employment type Fulltime Job function Research and Analyst Industries Pharmaceutical Manufacturing We look forward to receiving your application. More information about Novocure and our therapy can be found on our website at. Our employees benefit from an attractive package of benefits, which may vary depending on position and area of deployment. J-18808-Ljbffr 71404138 [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
Regulatory Affairs TALENT POOL
• AT- 9 Wien
Homeoffice möglich
[. .. ] of applications to health authorities. We also work closely with the Submission Management Group (SMG) in Pharma Technical Regulatory (PTR) as a document and data hub for [...]
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[...] 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 [. .. ] Regulatory Submission, Clinical Trial and related Regulatory Operation areas to support our teams Help to build a knowledge base and leverage best practices in the area of Regulatory Submissions, Clinical Trials and supporting activities Develop your mentoring skills by training new joiners or other team members Continuously improve process efficiency and support service quality exercises Build a wide network within the operation groups to ensuring smooth operations in different teams Who you are We are looking for someone who is selfmotivated, [. .. ] 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 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 [. .. ] a centralized location. They conduct remote and onsite monitoring, automate data analytics and riskbased 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 14.10.2025 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 [...]
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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 [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Induvidual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer [. .. ] 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 17.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
[. .. ] shape strategies with actionable tactics. Developing and delivering comprehensive product education and medicalscientific information. Supporting Key Account Managers (KAMs) in identifying and engaging influential experts in the [...]
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[...] field, and supporting clinical trials while ensuring compliance with local regulatory guidelines. Qualifications Proven experience in Medical Affairs or Medical Science in the aesthetics or dermatology field. Expertise in developing and delivering medical training programs. Demonstrated ability to operate compliantly in a fieldbased role, effectively collaborating within both the medical and commercial organizations. Strong knowledge [. .. ] We believe a flexible work environment is only attainable by building strong relationships based on trust with our employees. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Nordberg Medical by 2x. #J-18808-Ljbffr 69801330 [. .. ]
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 [. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities 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 [. .. ] 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
Medical Science Liaison m/w/d-Austria
• Wien
[. .. ] patients treated with Tumor Treating Fields (TT Fields) . Additional responsibilities includebut are not limited toacting as a scientific interface between the company and HCP communities regarding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] communication about Novocures clinical development plans as well as other research and development activities. Developing appropriate training materials, supporting external research projects related to marketed or investigational Novocure indications, and participating in field-based activities to advance existing products and introduce new indications are also part of the role. The MSL plays an important [. .. ] therapy awareness among prescribers and nonprescribers Manage the entire Austrian territory and all associated field activities Deliver medical training on Novocure products and disease areas Support and accompany investigator Sponsored Trials (ISTs) and other research projects Provide HCP insights and market information to the company Participate in medical (Europewide) congresses, and organize and follow up on advisory boards Promote scientific advancement related to TT Fields Support Phase 3 studies in collaboration with clinical teams and researchers Build and maintain relationships with [. .. ] minimum salary is 3, 682 gross per month. However, we are willing to offer a significantly higher salary. Seniority level Mid Senior level Employment type Fulltime Job function Research and Analyst Industries Pharmaceutical Manufacturing We look forward to receiving your application. More information about Novocure and our therapy can be found on our website at. Our employees benefit from an attractive package of benefits, which may vary depending on position and area of deployment. #J-18808-Ljbffr 71596926 [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Senior Analyst Clinical Site Contracts-German Polish speaker-Remote-FSP
[. .. ] and professionally. We recognize and value the importance of all people, the way we work, our drive for innovation and, most importantly, our patients. We are looking [...]
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[...] for a Senior Analyst Clinical Site Contracts, German Polish speaker to work 100 remotely in EU. The job is dedicated to one sponsor. This role will be part of the Site Contracts Budgets team, working to execute the clinical site contracts and budgets process for sponsor clinical development programs, from contract initiation to completion, maintenance, [. .. ] Pharma top 50. And we have an incredible pipeline of work. Expect exciting professional challenges in inspiring studies, but with time for your outside life. Responsibilities Negotiate and maintain Clinical Trials Agreements (CTA) , site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable contracts. As required, oversee CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols. Ensures compliance of contracts with Fair Market [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Medical Science Liaison-South Germany and Austria
• Saarbrücken, Saarland
[. .. ] identify local needs and shape strategies with actionable tactics. Develop and deliver comprehensive product education and medicalscientific information. Support Key Account Managers in identifying and engaging influential [...]
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[...] experts, and support clinical trials while ensuring compliance with local regulatory guidelines. Qualifications Proven experience in Medical Affairs or Medical Science in the aesthetics or dermatology field. Expertise in developing and delivering medical training programs. Demonstrated ability to operate compliantly in a fieldbased role, collaborating within both the medical and commercial organizations. Strong knowledge of [. .. ] team where innovation and creativity are actively encouraged. Remotefriendly position: Flexible work environment built on trust and strong relationships. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 69959222 [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Medical Science Liaison-North Germany
• Hannover, Niedersachsen
[. .. ] shape strategies with actionable tactics Developing and delivering comprehensive product education and medicalscientific information Supporting Key Account Managers (KAMs) in identifying and engaging influential experts in the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field, and supporting clinical trials while ensuring compliance with local regulatory guidelines This is a highly collaborative role, where you will be a part of a crossfunctional local team in the DACH region and Europe, as well as the global Medical Affairs team. As an early member of the Nordberg Medical team, youll have a [. .. ] We believe a flexible work environment is only attainable by building strong relationships based on trust with our employees. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Nordberg Medical by 2x. Get notified about new Medical Science Liaison jobs in Hannover, Lower Saxony, Germany. #J-18808-Ljbffr 69958517 [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Bremen
[. .. ] strategies with actionable tactics Developing and delivering comprehensive product education and medical-scientific information. Supporting Key Account Managers (KAMs) in identifying and engaging influential experts in the field, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supporting clinical trials while ensuring compliance with local regulatory guidelines. This is a highly collaborative role, where you will be a part of a cross-functional local team in the DACH region and Europe, as well as the global Medical Affairs team. As an early member of the Nordberg Medical team, youll have [. .. ] believe a flexible work environment is only attainable by building strong relationships based on trust with our employees. Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 69958256 [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Senior Field Medical Specialist-Region West-Mainz, Köln, Düsseldorf (m/w/d)
[. .. ] 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 [. .. ] updates on current research and clinical practices during product launches, customer meetings and training sessions. Clinical Research Support Support the clinical research teams to identify sites and investigators for clinical trials. Data Dissemination and Insights Gather information from KOLs on how they are using our products. Provide feedback to marketing and sales to help develop marketing materials and commercial strategy. Represent the company at scientific conferences, meetings, and advisory boards, communicating data and engaging in scientific discussions. Compliance and Reporting Ensure [. .. ] 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
• 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 [. .. ] to achieve data cut and lock deadlines. Provides feedback to line managers on staff performance including strengths as well as areas for development. May be assigned to larger, more complex trials. Qualifications Bachelors degree or RN in a related field or equivalent combination of education, training and experience. Demonstrated ability to lead and align teams in the achievement of project milestones. Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central) . Preferred [. .. ] 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 with [...]
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[...] 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) Flexible [. .. ]
Job am 05.11.2025 bei Jobleads gefunden
• 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 [...]
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[...] 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 [. .. ] Monitoring Board and/or Data Monitoring Committee activities. May lead projects involving integrated analyses, attend regulatory agency meetings or respond to questions to support the statistical analysis results of clinical trials on behalf of the sponsor. Follows applicable SOPs, WIs, and relevant regulatory guidelines (e. g. ICH) . Maintains well organized, complete, and uptodate project documentation, and verification/ quality control documents and programs; ensuring inspection readiness. Displays willingness to work with others and assists with projects and initiatives as necessary to [. .. ] 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 [. .. ] writer in the pharmaceutical/ biotech industry. Prior experience drafting documents for multiple indications, preferably in Bio NTechrelevant indications. Prior experience drafting new or updated CTPs and CSRs required for Phase IIII trials. Prior experience drafting highcomplexity variants of IBs, clinical CTDCTAIMPd/IND modules, and clinical CTDBLA/ MAA modules. Prior experience as lead medical writer for BLA/ MAA dossiers, ideally for Bio NTechrelevant indications. Prior experience managing small teams of writers supporting the drafting of BLA/ MAA dossiers. Prior experience drafting DSURs/ Annual Reports, [. .. ]
Job am 03.11.2025 bei Jobleads gefunden
• München, Bayern
Sponsor Dedicated
Clinical Trial Manager based in Munich area Are you a dynamic leader passionate about driving clinical
trials to success? We are looking for an experienced Clinical [...]
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[...] Trial Manager responsible for study oversight and delivery management (time, budget, quality) from startup to closure in Germany. In this role, youll collaborate with sponsors, investigators and crossfunctional teams to bring lifechanging treatments to patients. Key Responsibilities Manage clinical trial activities [. .. ] today and be part of a team that makes a difference Learn more about our EEO Accommodations request here. Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 68042454 [. .. ]
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 [...]
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[...] 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 [. .. ] EMA. Support and occasionally lead initiatives to improve drug development efficiency and harmonization, contributing to cost savings and shortened timelines. Skills and Qualifications Extensive experience in biostatistics within oncology clinical trials, with strong knowledge of regulatory requirements including FDA, EMA, and ICH guidelines. Proven expertise in statistical methods for survival analysis and proficiency with statistical software such as SAS and R. Experience managing CROs and leading crossfunctional project teams in a pharmaceutical environment. Masters degree in Statistics or Biostatistics required; Ph D [. .. ] 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
• 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 [. .. ] treatment networks to aid experts in uncovering people with rare genetic disease of obesity. Closely collaborate with Global Clinical Development and Operations on interactions with investigators participating in Rhythms clinical trials, investigator meetings and advisory boards. Support clinical trial execution attending to the needs of investigators. Triage pressure points that may impede progress of clinical studies to the cross functional team for timely resolution. Assist in identification and education of referral sites for clinical trials and investigators to drive trial enrolment. [. .. ] 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 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Medical Science Liaison Hematology/ Oncology (m/f/d) - Rheinland-Pfalz, Saarland, Süd-Hessen, . . .
[. .. ] Oncology (m/f/d) Territory: Rheinland-Pfalz, Saarland, Süd-Hessen, Nordwest-Baden-Würtemberg Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals with strong
clinical and/or scientific [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad medical/ scientific community. Essential Functions Of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans-identify, [. .. ] all activities related to medical information for external groups. Act as point of contact for unsolicited information requests on company inline products and pipeline. Facilitate company sponsored and investigator sponsored trials (ISTs) Provide frequent updates on investigative site support by updating medical/ clinical teams with feedback and insights from interactions and discussions with External Experts and investigators. Provide medical/ scientific leadership and expertise to internal and external groups Conduct internal trainings on medically relevant topics. Identify and nominate members of the [. .. ] have any questions or concerns or would like to exercise your rights. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Incyte by 2x Get notified about new Medical Science Liaison jobs in Germany. Medical Science Liaison Oncology North Germany (Senior) Medical Affairs Scientist (m/w/d) Field Specialty Care: Inflammation Immunology, Gebiet: Bayern Medical Affairs Clinician-Southern [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Associate Director, GCP Inspection Lead EMEA
Führungs-/ Leitungspositionen
[. .. ] business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. At Be One Medicines, we are dedicated to advancing the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] quality of global clinical trials through outstanding regulatory compliance and excellence. As the Inspection Lead reporting to the R D Quality, Sr. Director of Global GCP Inspection Management, youll be primarily responsible for GCP Health Authority inspection readiness for cross-functional clinical study teams, managing inspection logistics and process improvements to ensure research and development [. .. ] law. All employment is decided on the basis of qualifications, merit, and business need. Seniority level Seniority level Director Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Be One Medicines by 2x Get notified about new Associate Director Clinical Research jobs in Germany. Clinical Trial Manager Early Phase (f/m/d) Associate Director-Med Tech Clinical Operations Business Development Manager Life Sciences/ Clinical Research (m/w/d) [. .. ]
Job am 15.09.2025 bei Jobleads gefunden
CRA Germany-single client
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Overview CRA Germany-single client role at Syneos Health Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes. Core Focus Conduct thorough on-site and remote monitoring of clinical research studies Develop and implement tools, procedures, and processes to ensure quality monitoring Manage defined components of projects or processes within their area of responsibility Utilize practical [. .. ] through education combined with experience Maintain high standards of clinical practice and ensure the success of clinical trials Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology Get notified about new Clinical Research Associate jobs in Munich, Bavaria, Germany. Clinical Research Associate/ Senior Clinical Research Associate #J-18808-Ljbffr 62076447 [. .. ]
Job am 29.08.2025 bei Jobleads gefunden
Senior Statistical Programmer
• Frankfurt, Hesse
[. .. ] figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, [...]
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[...] analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADa M datasets, Tables, Figures, Listings and Analysis Submission content. Collaborates with study teams to ensure the quality and accuracy [. .. ] additional statistical analyses including but not limited to: support responses to regulatory agencies, generate integrated summary of safety and efficacy, support publications and presentations, support planning and reporting of clinical trials via exploratory analyses of available data, Position Qualifications and Experience Requirements: Education BSc in Computer Science, Mathematics, Statistics or related area with relevant experience Experience At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/ pharmaceutical environment using SAS Software. Indepth understanding of [. .. ] outcomes and population health worldwide. Learn more at https:/ / jobs. iqvia. com Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Senior Statistical Programmer jobs in Frankfurt, Hesse, Germany. Associate Principal Statistical Programmer (m/w/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, [. .. ]
Job am 01.07.2025 bei Jobleads gefunden
Clinical Trial Site Relationship Coordinator
• München, Bayern
Clinical Trial Site Relationship Coordinator Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain [. .. ] responsibilities as assigned, including site Qualification Visits, prepping/ consultation support for site audits, etc. Qualifications Minimum a Bachelor of Science in health-related field; Minimum 1 years site and clinical trials experience (more experience for the more senior positions required) ; CRA experience is an asset; Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred; Knowledge of medical terminology and clinical patient management preferred; Fluency in English; German; Demonstrated organizational and prioritization skills; Excellent oral and [. .. ] qualifications and, if interested, you will be contacted with details for next steps. Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Medpace by 2x Clinical Trial Associate/ Specialist (CTA/ CTS) Freelance Clinical Trials Site Coordinator Sponsor Dedicated Clinical Trial Assistant in Munich area Senior Clinical Research Associates (experienced) - Germany (Senior) Research Manager-Spine Neurosurgery Expert Clinical Trials [. .. ]
Job am 16.06.2025 bei Jobleads gefunden
Clinical Data Standards Manager
• Zürich
Join to apply for the
Clinical Data Standards Manager role at argenx Join to apply for the Clinical Data Standards Manager role at argenx Get AI-powered advice on this [...]
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[...] job and more exclusive features. Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for [. .. ] data standards development that includes industry standards and regulations. Set up, lead or/ and contribute actively in the Data Standards Governance meetings. Provide support to optimize data acquisition in clinical trials by exploring opportunities to streamline and integrate data, enhancing efficiency and data quality. Support and implement future strategies and technology-enabled processes and tools for clinical trials standards, change control management and the exchange of standards information to internal and external stakeholders. Keep abreast of Industry and Regulatory Authority requirements [. .. ] your privacy rights, please contact our Global Privacy Office by email at. 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 argenx by 2x Sign in to set job alerts for Clinical Data Manager roles. Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 52042805 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Analyst pro Jahr?
Als Clinical Trials Analyst verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Analyst Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 25 offene Stellenanzeigen für Clinical Trials Analyst Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Analyst Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Analyst Jobs werden derzeit in Bayern (9 Jobs), Niedersachsen (2 Jobs) und Saarland (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Analyst Jobs?
Clinical Trials Analyst Jobs gehören zum Berufsfeld Biotechnologie.
