19 Jobs für Clinical Trials Consultant
Stellenangebote Clinical Trials Consultant Jobs
Job vor 3 Tagen 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 gestern bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] FDA-approved treatments 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 [...]
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[...] in midtolatephase 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, [. .. ] interfaces with Research 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 Phase13 Clinical Trials for the clinical development in accordance with Neurocrine SOPs and GCP guidance Develops and implements 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 [. .. ] be able to effectively operate in a multilevel 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 preclinical through all clinical phases and product launch Neurocrine Biosciences is an EEO/ Disability/ Vets employer. We are committed to building [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Kaiseraugst, Aargau
[. .. ] with your statistical know-how. This includes optimizing decision-making in all discovery and development phases of our nutrition and care products by designing robust experiments and analyzing data [...]
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[...] from clinical trials or consumer studies. Integrate and analyze data from diverse sources (e. g. combining evidence from observational studies and randomized trials) to perform meta-analyses and develop a comprehensive evidence base for product development and marketing claims in nutrition and care. Collaborate closely with bioinformaticians in the team who analyze related [. .. ] oriented manner with colleagues across disciplines bioinformaticians, study directors, nutritionists, project managers, data managers, marketing teams, etc. either as a core project team member or as an ad-hoc statistical consultant, to ensure data-driven decision making. Participate in external collaborations on a global scale (with universities, research institutes, industry partners, CROs, etc. ) to stay at the forefront of nutritional research and statistical methodologies and to drive innovation in how we use data in nutrition and personal care research, e. [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Kaiseraugst, Aargau
[. .. ] with your statistical know-how. This includes optimizing decision-making in all discovery and development phases of our nutrition and care products by designing robust experiments and analyzing data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] from clinical trials or consumer studies. Integrate and analyze data from diverse sources (e. g. combining evidence from observational studies and randomized trials) to perform meta-analyses and develop a comprehensive evidence base for product development and marketing claims in nutrition and care. Collaborate closely with bioinformaticians in the team who analyze related [. .. ] oriented manner with colleagues across disciplines bioinformaticians, study directors, nutritionists, project managers, data managers, marketing teams, etc. either as a core project team member or as an ad-hoc statistical consultant, to ensure data-driven decision making. Participate in external collaborations on a global scale (with universities, research institutes, industry partners, CROs, etc. ) to stay at the forefront of nutritional research and statistical methodologies and to drive innovation in how we use data in nutrition and personal care research, e. [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Frankfurt, München, Berlin, Hesse, Bayern
[. .. ] leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early [...]
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[...] science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit and follow us on X (formerly Twitter; Blueprint Meds) and Linked In. Blueflex is our operating model which optimizes culture, productivity, flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility. Blueflex allows [. .. ] will be performed? Select. . . Are you currently providing or have you ever provided services to any Blueprint Medicines entity, whether as an employee, a temporary worker or a consultant? Select. . . I agree to receive updates about new job opportunities matching my applicant profile and marketing communications. Select. . . Privacy Policy Acknowledgement Select. . . Please read the Privacy Policy to understand how Blueprint Medicines may collect and process personal data associated with your application. #J-[. .. ]
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
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 22.02.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] end platform with biosimulation, regulatory science, and market access solutions combined with our strong team of scientists and subject matter experts enable our clients to have: Informed [...]
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[...] decision-making reduced clinical trial burden Higher R D productivity Improved patient outcomes increased patient access to medicines Accelerated regulatory approval Responsibilities: Our Pharmacometricians are responsible for supporting quantitative decision-making in drug development through the development and application of population PK, PK/ PD, exposure-response and other models. Qualified candidates will have the [. .. ] interests. Support projects for Certaras clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications: Ph D, MD, Pharm D in [. .. ] meta-analysis, dose-response and exposure-response analyses, dataset creation, disease modeling, trial simulation, optimal study designs, strategic decision analyses, economic modeling) . Experience in moving compounds through the clinical trials process and experience with various elements of clinical development and trial design and management and filings preferred. Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, [. .. ]
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 [. .. ]
Job am 12.01.2026 bei Jobleads gefunden
Consultant Clinical Affairs
• 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, [...]
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 16.12.2025 bei Jobleads gefunden
(Senior) Consultant, Qualified Person
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Position title (Senior)
Consultant, Qualified Person Description Granzer Pharmaceutical Services Gmb H was founded in 2022 as a spin-off of Granzer Regulatory Consulting Services Gmb H. We are a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Pharmaceutical Service Provider and Consultancy for the Development, Manufacturing and Quality Assurance of Medicinal Products. Our focus is the EU Import, Storage, Distribution and EU-Release of Investigational Medicinal Products, supporting the Clinical Trials of our Clients. For our team in Munich, we are looking for a (Senior) Consultant, Qualified Person Responsibilities Act as (deputy) Qualified Person under Granzers manufacturing authorisation Provide expertise and consulting on GMP-related items to our clients Support the import and batch release processes for client products Perform GMP/ [. .. ]
Job vor 5 Tagen bei Neuvoo gefunden
Enovis
Director, Medical Affairs
• Freiburg, Baden- Wurttemberg
Führungs-/ Leitungspositionen
Wer wir sind ÜBER ENOVIS Who We Are ABOUT ENOVIS Was Sie tun werden What Youll Do Oversees the direction, planning, execution and interpretation of
clinical trials/ research and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 7 Tagen bei Neuvoo gefunden
Tech Biz Global GmbH
Principal Statistical Programming Consultant (EU)
• Aachen, North Rhine- Westphalia
Beratungs-/ Consultingtätigkeiten
At Tech Biz Global, we are providing recruitment service to our TOP clients from our portfolio. We are currently seeking a Principal Statistical Programming
Consultant (EU) to join one [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of our clients teams. If youre looking for an exciting opportunity to grow in a innovative environment, this could be the perfect fit for you. In this role, you will work under the direction of the Team Lead or Project Manager and be responsible for delivering high-quality statistical programming outputs for clinical trials, including early-phase studies, publications, and regulatory submissions. Key Responsibilities Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications Lead at least one study team, providing technical and domain expertise Manage and mentor a small team of 24 programmers (if required) Develop and validate SAS [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Tech Biz Global GmbH
Principal Statistical Programming Consultant (EU)
• Greifswald, Mecklenburg- Vorpommern
Beratungs-/ Consultingtätigkeiten
At Tech Biz Global, we are providing recruitment service to our TOP clients from our portfolio. We are currently seeking a Principal Statistical Programming
Consultant (EU) to join one [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of our clients teams. If youre looking for an exciting opportunity to grow in a innovative environment, this could be the perfect fit for you. In this role, you will work under the direction of the Team Lead or Project Manager and be responsible for delivering high-quality statistical programming outputs for clinical trials, including early-phase studies, publications, and regulatory submissions. Key Responsibilities Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications Lead at least one study team, providing technical and domain expertise Manage and mentor a small team of 24 programmers (if required) Develop and validate SAS [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
IQVIA
Principal Biostatistician, Medical Affairs (FSP-Permanent Homebased)
• Frankfurt, Hessen
[. .. ] and reporting in support of pharmaceutical development and regulatory submissions. Serve as a resource for the department, ensuring scientific integrity and regulatory compliance in the application of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] statistical methodology to clinical trials. Participate as lead statistician on major projects, including contributing to clinical development plans, developing/ reviewing protocols, preparing/ reviewing analysis plans, overseeing the conduct of analyses, preparing/ reviewing integrated clinical and statistical reports, and responding to regulatory queries. Key Responsibilities: Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee Participate in independent research activities, teaching opportunities, presentations, and preparation of [. .. ]
Job am 10.03.2026 bei Neuvoo gefunden
Hays
Clinical Trial Associate für den Bereich Quality Assurance (m/f/d)
• Frankfurt, Hessen
Angebote von Zeitarbeitsunternehmen
Clinical Trial Associate für den Bereich Quality Assurance (m/f/d) Arbeitnehmerüberlassung Greater Frankfurt area Start date: asap Reference number: 821921/ 1 Diesen Job teilen oder drucken Responsibilities Quality Oversight Systems Management:Monitor [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance with quality guidelines in clinical business areas and implement regional quality plans Identify potential gaps, recommend solutions, and [. .. ] 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 Profile Education Experience: Bachelors 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 [. .. ]
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 19 offene Stellenanzeigen für Clinical Trials Consultant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Consultant Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Clinical Trials Consultant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Consultant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Consultant Stellenangebote:
- Tech Biz Global GmbH (2 Jobs)
- Enovis (1 Job)
- IQVIA (1 Job)
- Hays (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Consultant Jobs werden derzeit in Nordrhein-Westfalen (4 Jobs), Bayern (4 Jobs) und Hessen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Consultant Jobs?
Clinical Trials Consultant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
