Clinical Trials Analyst Stellenangebote


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14 Jobs für Clinical Trials Analyst


Stellenangebote Clinical Trials Analyst Jobs


Job am 17.11.2025 bei Jobleads gefunden

Medical Science Liaison-South Germany and Austria

• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

Data Analyst (f/m/d)

• Berlin Clariness is looking for a Data Analyst (f/m/d) based in Berlin or Hamburg. -Full-time; unlimited-About the role This role focuses on transforming data into meaningful insights that help teams make [...]
MEHR INFOS ZUM STELLENANGEBOT[...] confident, informed decisions. Youll contribute to business impact by building intuitive dashboards, conducting thoughtful analyses, and working closely with stakeholders to ensure data [. .. ] and challenging projects. A supportive and open company culture, providing the opportunity to collaborate with a diverse and professional team. Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster. Application Process Apply via link (CV only; no cover letter required) . Introductory call (30 min) Technical interview Take Home Test Demo Day Decision. We aim to move promptly and keep you updated at every step. At Clariness, we are proud to be [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden

Senior Analyst, Site Contracts and Budgets Germany, Poland, Portugal or UK FSP

• Berlin When our values align theres no limit to what we can achieve. At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT[...] consulting and market access every clinical development solution we provide is underpinned by a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and are committed to making a difference. Parexel is currently seeking a Senior Analyst Site Contracts Budgets to join us in either Germany, Poland, Portugal or the UK dedicated to a single 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, [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden

Principal Scientist as Biomarker Lead for Neuroscience and Mental Health

• Biberach an der Riß, Baden- Württemberg Führungs-/ Leitungspositionen Principal Scientist as Biomarker Lead for Neuroscience and Mental Health Were looking for a motivated Principal Scientist to help shape the future of clinical development in the field of neurodegeneration, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] psychiatry, and mental health. As a Principal Scientist, you will play a key role in driving innovative translational strategies across the entire clinical development pipeline, with the ultimate goal of being firsttopatients. In this strategic position, you will support the clinical drug research and [. .. ] analyses for decision making throughout clinical drug development and registration, including all necessary processes and documentation. Act as representative in trial and project teams and regulatory meetings. Lead clinical development trials and project overarching topics in Experimental Medicine, and represent the respective area of responsibility in internal and external initiatives/ working groups. Implement collaborations and strategic partnerships with external bodies, and organize and manage projects with external organizations such as CROs and AROs. Continuously develop and refine functional processes and infrastructure. [. .. ] guaranteed to be considered. Step 2: Virtual meeting mid/end of January2026. Step 3: Onsite interviews beginning/ mid February2026. Seniority level Mid Senior level Employment type Parttime Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 73203770 [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden

CRA Germany or Austria-single-client

• München, Bayern Beratungs-/ Consultingtätigkeiten [. .. ] job and more exclusive features. Description CRA Germany or Austria-single-client Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate [...]
MEHR INFOS ZUM STELLENANGEBOT[...] unique 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 we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work [. .. ] 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. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ] or 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 Fulltime Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at Syneos Health by 2x #J-18808-Ljbffr 72511034 [. .. ]

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Job am 08.12.2025 bei Jobleads gefunden

Senior Statistical Programmer (Remote-Permanent Homebased)

• 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 Collaborate with 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. Ensure the quality and accuracy thus submission readiness of clinical data [. .. ] 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 [. .. ] medical treatments to help improve patient outcomes and population health worldwide. Learn more at https:/ / jobs. iqvia. com Seniority level Mid Senior level Employment type Fulltime Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care #J-18808-Ljbffr 71992279 [. .. ]

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Job am 04.12.2025 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 [. .. ]

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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 [. .. ]

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Job am 18.11.2025 bei Jobleads gefunden Medical Science Liaison-North Germany • 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [. .. ] 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 [. .. ]

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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 [. .. ] 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 [. .. ]

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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 [. .. ]

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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, [...]
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 [. .. ] 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, [. .. ]

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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 14 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 (3 Jobs), Berlin (2 Jobs) und Baden-Württemberg (2 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Trials Analyst Jobs?

Clinical Trials Analyst Jobs gehören zum Berufsfeld Biotechnologie.


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Dauer: 0.042 s., Vers. V.2025-d-2007-Ind-141