13 Jobs für Clinical Trials Consultant
Stellenangebote Clinical Trials Consultant Jobs
Job am 23.03.2026 bei Jobleads gefunden
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit Was Sie tun werden What Youll Do Oversees the direction, planning, execution [...]
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[...] and interpretation of clinical trials/ research and data collection activities along with regulatory compliance, patient safety and emerging patient risks. May establish and approve scientific methods for design and implementation of clinical protocols, data collection systems and final reports. Provides input on clinical study design, execution, and data analysis. Leads the adverse event reporting and [. .. ] and develops information for reports submitted to regulatory agencies. Monitors adherence to protocols and determines study completion. May recruit clinical investigators and negotiate study design and costs. May act as consultant/ liaison with other corporations when working under licensing agreements. Establishes strategic plans and objectives. Participates in development of methods, techniques and evaluation criteria for programs and individuals. Decisions have a serious impact on the overall success of functional, business unit or company objectives. Directs functional area through department Managers and/[. .. ]
Job am 26.01.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] in Munich, Germany. We provide comprehensive development and manufacturing services for drug products, including sterile and non-sterile liquids, solids, and semi-solids. Our expertise also covers biologicals, orphan [...]
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[...] drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply. With production sites in Germany, France, Greece, Norway, Japan, and Switzerland, we ensure high-quality manufacturing across all stages of the drug development process. Founded in 2020, Adragos Pharma has rapidly grown through an [. .. ] to the Group COO, with close collaboration with the CEO and founder. It requires leadership, structure, and a strong bias for execution. We are seeking a former top-tier strategy consultant or operational transformation leader with solid experience in pharmaceutical manufacturing or CDMO environments. You must have worked on complex post-merger integrations or site transformations. You combine analytical strength with a pragmatic, entrepreneurial approach. Your mission Lead the integration of newly acquired manufacturing sites into the Adragos network; manage the [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
• Kassel, Hessen
Führungs-/ Leitungspositionen
[. .. ] teams in assay development and validation which includes semiquantitative as well as quantitative assays Support/ consult our project management and business development team as well as our [...]
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[...] clients Evaluation of clinical trial specimens Act as a trainer for external pathologists within our post approval services for the interpretation/ scoring of novel biomarkers Preparation of publications/ posters in collaboration with our customers Position Qualifications (Education, Skills, Experience) : Board certification (German board certification preferred) Additional training in Cytology Experience in hematopathology and/[. .. ] on oncology and immunology Excellent knowledge in IHC, m IF, FISH, RNA in situ hybridization to support the assay development team as well as to act as an experienced reader and consultant for customers in clinical trials. Experience in digital imaging applications and the evaluation of biomarkers via digital image analysis software Teamplayer Willingness to work in a GCLP environment Compensation and Benefits: Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Hays Professional Solutions GmbH
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Angebote von Zeitarbeitsunternehmen
Ihre Aufgaben: Quality Oversight Systems Management: Monitor compliance with quality guidelines in
clinical business areas and implement regional quality plans Identify potential gaps, recommend solutions, and escalate relevant issues Assist [...]
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[...] in maintaining and improving quality documents and processes Audit Inspection: Lead and support audit and inspection preparations, including document management and response coordination Ensure trial sites and teams are inspection-ready Consultation Collaboration:Serve as the primary quality consultant, providing guidance on regulatory requirements and risk management Support root cause analysis, CAPA processes, and audit planning Collaborate with quality teams to strengthen quality culture and resolve issues Process Improvement Metrics: Drive continuous improvement and process optimization Analyze quality metrics to identify gaps and recommend corrective actions to enhance compliance and efficiency Ihre Qualifikationen: Education Experience: Bachelor s degree in science, technology, or healthcare; experience in quality systems within clinical trials is required Project Management: Strong ability to prioritize and effectively manage multiple tasks Communication: Excellent communication skills and ability to influence various stakeholders Analytical Skills: Problem-solving abilities and attention to detail for risk assessment and process optimization Teamwork Flexibility: Independent yet collaborative work style within global teams Preferred: Experience [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
Senior
Consultant and Statistician (Patient Centered Research) m/w/d page is loaded # # Senior Consultant and Statistician (Patient Centered Research) m/w/dlocations: Frankfurt, Hesse, Germany: Reading, Berkshire, United Kingdom: Amsterdam, Netherlands: [...]
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[...] London, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 1, 2026 (27 [. .. ] left to apply) job requisition id: R1542495Senior Consultant and Statistician, Patient-Centered Research Overview At IQVIA, the Patient Centered Solutions team helps clients generate robust evidence on the patient experience across clinical development, regulatory submissions, and scientific dissemination. Our Statistics Psychometrics team specializes in the analysis of clinical outcome assessment (COA) and patient-reported outcomes (PRO) data, combining scientific rigor with strategic consulting to support high-impact decisions in drug development. The Role As a Senior Consultant, you will lead or support [. .. ] related quantitative field. 5+ years of relevant experience in the pharmaceutical, biotech, CRO, healthcare, or consulting environment. Advanced knowledge of complex statistical methods that apply to Phase I-IV clinical trials (multivariate analysis, regression analysis, logistic analysis, survival analysis, mixed models repeated measures, etc. ) Familiarity with SAS and/or R. Excellent written and verbal communication skills, strong attention to detail, and the ability to work effectively in a collaborative, matrixed environment. Why Join Us This role offers the opportunity to [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Essen, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
What Youll Do Qserve is seeking a
Consultant Clinical Affairs with strong medical writing skills and expertise in systematic literature searching and clinical evaluation of medical devices. In this role, [...]
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[...] you will support clients in navigating complex regulatory landscapes for devices of different risk classes. You will work closely with global experts to ensure compliance and market access for [. .. ] clinical outcome parameters and acceptance criteria to support the clinical claims of the devices. Perform design and appraisal of systematic literature searches on multiple databases (Pub Med, Science Direct, Clinical Trials and others) , including adverse event ones, such as MAUDE, FDA Medical Device Recalls and similar. Elaborate, update and peer review Clinical Evaluation Plans (CEPs) , Clinical Evaluation Reports (CERs) and Literature Search Reports (LSRs) . Write stateoftheart (SOTA) text based on selected data. Ensure that peer review of any [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] for tardive dyskinesia, chorea associated with Huntingtons disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid-to [...]
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[...] late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, [. .. ] and Business Development to assess new product opportunities, develop clinical research strategy and product development plans. Your Contributions (include, but are not limited to) : Directs Phase 1-3 Clinical Trials for the clinical development in accordance with Neurocrine SOPs and GCP guidance Develops and implement study protocols consistent with the Development Team direction Assists in the identification and selection of clinical investigators for clinical trials Maintains appropriate communication and professional relationship with NBI Clinical Investigators Conducts assessment and disposition of [. .. ] able to effectively operate in a multi-level matrix corporate environment, requiring interaction with, and/or direction of, internal and external personnel, including physicians, scientists, monitors, administrative, regulatory, commercial, and consultant personnel Expertise in the areas of drug development, operations and strategic planning Expertise in submissions from investigational new drug through new drug application filings and managing a product from pre-clinical through all clinical phases and product launch Neurocrine Biosciences is an EEO/ Disability/ Vets employer. We are committed to [. .. ]
Job am 07.04.2026 bei Jobleads gefunden
• Uetze, Niedersachsen
Beratungs-/ Consultingtätigkeiten
[. .. ] security and additional career opportunities that working for a global CRO can bring? Our team says its the best of both worlds. Clin Choice is searching for [...]
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[...] a Senior Biostatistician Consultant to join one of our clients. Clin Choice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the [. .. ] skills, with ability to effectively communicate internally and with clients. Demonstrated understanding and insight in statistics, drug development process and relevant FDA regulations. Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications [. .. ]
Job am 07.04.2026 bei Jobleads gefunden
• Uetze, Niedersachsen
Beratungs-/ Consultingtätigkeiten
[. .. ] additional career opportunities that working for a global CRO can bring? Our team says its the best of both worlds Clin Choice is currently recruiting for a [...]
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[...] Manager, Statistical Programming Consultant to join our clients team an exciting opportunity to lead impactful statistical strategy in a dynamic environment. Role Overview We are seeking an experienced and motivated Manager, Statistical Programming to lead programming activities within the Biometrics group. This role will oversee clinical programming deliverables, drive quality and compliance, support regulatory submissions, and mentor a team of programmers. The ideal candidate will have strong expertise in SAS (and/or R ) , deep knowledge of CDISC standards, experience with oncology clinical trials, and excellent leadership skills. Key Responsibilities: Leadership Strategy Lead and mentor a team of statistical programmers, fostering development and high performance. Oversee internal and vendor/ CRO programming deliverables, ensuring timelines and quality expectations are met. Establish and maintain programming standards, documentation, and best practices. Support planning, resourcing, and prioritization for [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Beratungs-/ Consultingtätigkeiten
Consultant-Clinical Operations (Remote-Europe) Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. We surpassed 2B in revenue in our [...]
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[...] last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right [. .. ] the office, so you can thrive in your ideal environment. The Role Veeva Systems is looking for Consultants and Senior Consultants who have some content management expertise and/or clinical trials expertise and/or software implementation expertise. As a member of our Professional Services team, you will be responsible for understanding our customers challenges and clinical needs, translating requirements into solution design, delivering training, and supporting customers during application validation. If you are a Senior Consultant, you will also be leading [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Development Director DE
• München, Bayern
Führungs-/ Leitungspositionen
Position: Brand Ambassador/ Cryptocurrency Analytics
Consultant Location: Your City Germany (On-site) About the Company: Assetara Limited is a global leader in AI-powered financial analytics and trading solutions. We are [...]
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[...] committed to innovation excellence and expanding our presence across Asia Europe and the USA through a dynamic and client-focused team. Job Brief We are [. .. ] your city of residence in the USA. How to Apply Submit your resume and a brief cover letter through our career page or email. Key Skills Fundraising Management Experience Biotechnology Clinical Development Clinical Trials Research Development Training Development Grant Writing Economic Development Leadership Experience Public Speaking Product Development Employment Type Full Time Experience years Vacancy 1 Monthly Salary Salary 1000-10000 #J-18808-Ljbffr 83216836 [. .. ]
Job am 13.01.2026 bei Jobleads gefunden
Consultant Clinical Affairs
• Dortmund, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
What Youll Do Qserve is seeking a
Consultant Clinical Affairs with strong medical writing skills and expertise in systematic literature searching and clinical evaluation of medical devices. In this role, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will support clients in navigating complex regulatory landscapes for devices of different risk classes. You will work closely with global experts to ensure compliance and market access for [. .. ] clinical outcome parameters and acceptance criteria to support the clinical claims of the devices. Perform design and appraisal of systematic literature searches on multiple databases (Pub Med, Science Direct, Clinical Trials and others) , including adverse event ones, such as MAUDE, FDA Medical Device Recalls and similar. Elaborate, update and peer review Clinical Evaluation Plans (CEPs) , Clinical Evaluation Reports (CERs) and Literature Search Reports (LSRs) . Write stateoftheart (SOTA) text based on selected data. Ensure that peer review of any [. .. ]
Job am 13.01.2026 bei Jobleads gefunden
Consultant Clinical Affairs
• Köln, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
What Youll Do Qserve is seeking a
Consultant Clinical Affairs with strong medical writing skills and expertise in systematic literature searching and clinical evaluation of medical devices. In this role, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will support clients in navigating complex regulatory landscapes for devices of different risk classes. You will work closely with global experts to ensure compliance and market access for [. .. ] clinical outcome parameters and acceptance criteria to support the clinical claims of the devices. Perform design and appraisal of systematic literature searches on multiple databases (Pub Med, Science Direct, Clinical Trials and others) , including adverse event ones, such as MAUDE, FDA Medical Device Recalls and similar. Elaborate, update and peer review Clinical Evaluation Plans (CEPs) , Clinical Evaluation Reports (CERs) and Literature Search Reports (LSRs) . Write stateoftheart (SOTA) text based on selected data. Ensure that peer review of any [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Consultant pro Jahr?
Als Clinical Trials Consultant verdient man zwischen EUR 50.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 13 offene Stellenanzeigen für Clinical Trials Consultant Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Consultant Jobs werden derzeit in Niedersachsen (4 Jobs), Nordrhein-Westfalen (3 Jobs) und Hessen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Consultant Jobs?
Clinical Trials Consultant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
