9 Jobs für Clinical Trial Consultant
Stellenangebote Clinical Trial Consultant Jobs
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/or [. .. ] 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 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Stenoly is a fast-growing Norwegian health-tech company building AI-powered ambient
clinical documentation. Our platform listens to patient consultations and automatically generates structured clinical notes saving clinicians hours of administrative work [...]
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[...] every day. We serve hundreds of paying customers across Scandinavia, and were now expanding into the Austrian market. The Role Were hiring 4 Sales Development Representatives (Consultants) to spearhead our launch in Austria. Youll be the first point of contact for clinics and healthcare providers across the country responsible for generating interest, nurturing prospects through trial, and converting them into long-term customers. This is a consultant engagement, ideal for someone who thrives in an entrepreneurial, high-autonomy environment and wants to be part of building something from the ground up in a new market. What Youll Do Conduct targeted outreach to clinics, general practitioners, and healthcare providers across Austria Qualify inbound leads and manage follow-up [. .. ]
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 [. .. ] 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. g. regarding causal inference and target trial emulation. Oversee the outsourcing of data analyses to external partners and ensure that all analyses meet our quality standards and adhere to relevant guidelines and regulations. Work on a broad variety of projects and questions and handle competing priorities in a dynamic environment. We offer: A broad variety of projects, [. .. ]
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 [. .. ] 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. g. regarding causal inference and target trial emulation. Oversee the outsourcing of data analyses to external partners and ensure that all analyses meet our quality standards and adhere to relevant guidelines and regulations. Work on a broad variety of projects and questions and handle competing priorities in a dynamic environment. We offer A broad variety of projects, [. .. ]
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 ability [. .. ] 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 [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Tech Biz Global GmbH
• 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 [...]
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[...] 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 [. .. ] Science Statistics Biostatistics Life Sciences or related field Experience Minimum 5+ years of SAS programming experience in clinical trials Mandatory experience in Oncology Therapeutic Area (TA) Experience working with clinical trial data and regulatory submissions Technical Skills Strong proficiency in SAS programming Hands-on experience with: CDISC standards (SDTM, ADa M) Data migration and transformation TLF generation (Tables, Listings, Figures) Understanding of: Drug development lifecycle Regulatory requirements (e. g. , FDA, EMA) Soft Skills Ability to work independently and manage multiple priorities [. .. ]
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 [...]
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[...] 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 [. .. ] Science Statistics Biostatistics Life Sciences or related field Experience Minimum 5+ years of SAS programming experience in clinical trials Mandatory experience in Oncology Therapeutic Area (TA) Experience working with clinical trial data and regulatory submissions Technical Skills Strong proficiency in SAS programming Hands-on experience with: CDISC standards (SDTM, ADa M) Data migration and transformation TLF generation (Tables, Listings, Figures) Understanding of: Drug development lifecycle Regulatory requirements (e. g. , FDA, EMA) Soft Skills Ability to work independently and manage multiple priorities [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
IQVIA
• 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 [...]
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[...] 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 [. .. ] and initiate methodology development work with regards to statistical standards and validation procedures Consult onoperational/ statistical/ therapeuticarea topics Knowledge Sharing: Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses Performs as subject matter expert (SME) Risk Management: Identifies risks to project delivery and/or quality, leads in a way to minimize risks Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions Lock and Unblinding [. .. ]
Job am 10.03.2026 bei Neuvoo gefunden
Hays
• 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 [...]
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[...] compliance with quality guidelines in clinical business areas and implement regional quality plans Identify potential gaps, recommend solutions, and escalate [. .. ] 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 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Consultant pro Jahr?
Als Clinical Trial Consultant verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Clinical Trial Consultant Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Consultant Jobs werden derzeit in Hessen (3 Jobs), Sachsen-Anhalt (3 Jobs) und Mecklenburg-Vorpommern (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Consultant Jobs?
Clinical Trial Consultant Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
