9 Jobs für Clinical Trial Analyst
Stellenangebote Clinical Trial Analyst Jobs
Job vor 10 Tagen bei Jobleads gefunden
Global
Clinical Trial Lead FSP Remote Parexel is actively recruiting for a Global Trial Manager/ Study Manager to join us in either Austria or Germany. In this role you will [...]
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[...] provide leadership and direction to the trial team and be accountable for the overall success and delivery of your assigned clinical trial according [. .. ] and implement strategic direction and guidance for respective clinical studies. Effective communication skills via verbal, written, and presentation abilities. Seniority level Mid Senior level Employment type Fulltime Job functions Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing, Biotechnology Research, Hospitals and Health Care #J-18808-Ljbffr 78342375 [. .. ]
Job am 11.01.2026 bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] Responsibilities Review datasets in submission-ready ADa M format, including tables, figures, listings, and submission packages. Design, develop, and quality-control SAS programs to access, extract, transform, review, analyze, [...]
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[...] and submit clinical data for requested analyses. Collaborate with study teams to design data structures and specifications for ad hoc and study deliverables (ADa M datasets, Tables, Figures, Listings, and Analysis Submission content) . Ensure quality and accuracy for submission-ready clinical data (SDTM, ADa M, tables, figures, listings, define. xml) as required by authorities. [. .. ] of ISS and ISE datasets and associated output when not provided by CRO. Lead and oversee the design and implementation of complex SAS programs to analyze and report complex clinical trial data in CDISC ADa M format. Lead and oversee the development of global tools to increase efficiency and capacity of the Statistical Programming group. Work with clinical study teams to plan and execute activities to meet project timelines with high-quality deliverables. Collaborate with CR D staff regarding data analysis requests [. .. ] and manage timelines to meet goals Experience working in cross-functional, multicultural, international clinical trial teams Employment details Seniority level: Mid-Senior level Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Hospitals and Health Care IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. Learn more at https:/ / jobs. iqvia. com #J-18808-Ljbffr 74507458 [. .. ]
Job am 10.01.2026 bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] teams to design data structure and specifications for ad hoc and study deliverables including ADa M datasets, tables, figures, listings and analysis submission content. Ensures the quality [...]
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[...] and accuracythus submission readinessof clinical data as required by authorities (SDTM, ADa M, tables, figures, listings, define. xml) . Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead, study statisticians, and the clinical programming teams legacy data. Leads and oversees the inhouse specification and delivery of ISS and ISE datasets and associated output when not provided by CRO. Leads and oversees the design and implementation of complex SAS programs for applications that analyze and report clinical trial data in CDISC ADa M format. Develops global tools that increase the efficiency and capacity of the Statistical Programming group. Works closely with clinical study teams to plan and execute activities that meet project timelines with highquality deliverables. Additional Tasks Collaborates with CR D staff regarding data analysis requests. Performs additional [. .. ] a team, meeting set goals by managing own timelines. Experience working in crossfunctional, multicultural and international clinical trial teams. Seniority Level Mid Senior level Employment Type Fulltime Job Function Research, Analyst, and Information Technology Industries Hospitals and Health Care IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and [. .. ]
Job am 02.01.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] is a handson leadership role. As the primary architect of our discovery engine, you will focus on the biological why and the technical how before a molecule [...]
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[...] ever reaches a clinical trial. Translate Research into Therapy: Leverage Deep Pictions understanding and knowhow of Long Covid disease mechanisms to pivot from highimpact research to a viable, differentiated, patentable therapeutic approach. Delivery Precision: Together with our experts, lead the integration of innovative delivery systems to ensure candidates reach the right targets, and build the [. .. ] + speed: Clear goals, clear ownership, fast decisions. We build lightweight process that increases velocity instead of slowing it down. Seniority level Director Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr 73789014 [. .. ]
Job am 26.12.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen Freiberuflich
Lead
Clinical Research Associate-Freelance 3 days ago Be among the first 25 applicants About This Role TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners [...]
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[...] with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes fullservice capabilities, resourcing, and Functional Service Provider (FSP) solutions. The Freelance Lead Clinical Research Associate (Lead CRA) is responsible for leading and overseeing sitelevel clinical trial activities in Germany, ensuring studies are conducted in compliance with ICHGCP, local regulations, sponsor SOPs, and project timelines. As part of our SRS/ FSP team, you will be dedicated to one sponsor, a global pharmaceutical company recognized as an industry leader in innovative drug development across multiple therapeutic areas. Please [. .. ] aligning on these values, we foster a culture of collaboration, innovation, and excellencetogether making a difference for patients worldwide. Seniority level Mid Senior level Employment type Contract Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at TFS Health Science by 2x Sign in to set job alerts for Lead Clinical Research Associate roles. CRA II-single sponsor-Eastern Germany/ Northern Bavaria Were unlocking community knowledge in a new way. Experts add insights directly [. .. ]
Job am 19.12.2025 bei Jobleads gefunden
• Bonn, Nordrhein- Westfalen
Homeoffice möglich
[. .. ] function Other Industries IT Services and IT Consulting Referrals increase your chances of interviewing at adesso SE by 2x Sign in to set job alerts for Summer [...]
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[...] Staff roles. Freelance Clinical Trial Site Coordinator Cologne, North Rhine-Westphalia, Germany 1 week ago Trainee-Programm Financial Consultant (BWL, Finanzen, VWL) (w/m/d) Cologne, North Rhine-Westphalia, Germany 5 days ago Pedagogical specialist-elementary school child care Cologne, North Rhine-Westphalia, Germany 1 day ago Working Student Finance Procurement (m/f/x) Cologne, [. .. ] day ago Sankt Augustin, North Rhine-Westphalia, Germany 4 days ago Cologne, North Rhine-Westphalia, Germany 3 days ago Cologne, North Rhine-Westphalia, Germany 6 days ago UN Women: Coordination Analyst, UNTF to EVAW, Bonn, P-2 (Temporary Appointment) Bonn, North Rhine-Westphalia, Germany 5 days ago Cologne, North Rhine-Westphalia, Germany 3 days ago Bonn, North Rhine-Westphalia, Germany 3 days ago Overath, North Rhine-Westphalia, Germany 6 days ago Cologne, North Rhine-Westphalia, Germany 3 weeks ago Cologne, North [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Bremen
[. .. ] will be pivotal in establishing and nurturing relationships with key medical experts in North Germany. Youll work closely with KOLs, physicians, and healthcare professionals (HCPs) to lead [...]
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[...] scientific discussions, support trial enrollment, and deliver educational programs and training. As the primary medical point of contact, you will leverage your scientific expertise to strengthen collaboration with the Key Account Management team and drive impactful customer engagement. You Will Mostly Work On Building and maintaining strong peer-to-peer relationships with KOLs Leading [. .. ] 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, 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 [. .. ] 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 09.10.2025 bei Jobleads gefunden
• Holzkirchen, Bayern
Führungs-/ Leitungspositionen
Global Head of
Clinical Development Patient Safety Solutions Join to apply for the Global Head of Clinical Development Patient Safety Solutions role at Sandoz in Deutschland Global Head of Clinical [...]
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[...] Development Patient Safety Solutions 1 day ago Be among the first 25 applicants Join to apply for the Global Head of Clinical Development Patient [. .. ] provide regular updates and feedback to stakeholders. Minimum Requirements What youll bring to the role: Experience 10-15 years experience in a Clinical Development Patient Safety stakeholder engagement or business analyst role. Proven track record in project management and stakeholder satisfaction related to Clinical Development Patient Safety. Tenure in a management role overseeing complex projects. Proven track record of developing and implementing Clinical Development Patient Safety technology strategies. Demonstrated ability to lead and mentor a dispersed technology team. Experience in regulatory [. .. ] stakeholder engagement and relationship management. Skills Expert knowledge of Clinical Development Patient Safety business processes and complexities Strong experience implementing and managing IT technologies supporting key business capabilities, incl. Clinical Trial Management Systems (CTMS) , Electronic Data Capture (EDC) , Safety Databases (e. g. , Argus, Aris Global) , and Signal Detection, etc. Deep understanding of clinical trial processes, regulatory requirements (e. g. , Gx P, ICH guidelines) , and safety data management. A proven track record of implementing digital solutions to [. .. ]
Job am 29.08.2025 bei Jobleads gefunden
• 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] output (tables, figures and listings) when not provided by CRO. Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADa M format. Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables. Additional tasks: Collaborates with [. .. ] 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, [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical trial analyst pro Jahr?
Als Clinical trial analyst verdient man zwischen EUR 40.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Analyst Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Clinical Trial Analyst Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Analyst Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Analyst Jobs werden derzeit in Bayern (3 Jobs), Nordrhein-Westfalen (1 Jobs) und Bremen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Analyst Jobs?
Clinical Trial Analyst Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
