13 Jobs für Clinical Trials Consultant
Stellenangebote Clinical Trials Consultant Jobs
Job vor 3 Tagen bei Jobleads gefunden
• Baden- Württemberg
Consultant Medical Devices QARA United States Europe Quality Regulatory Affairs Manager Class III Cardiovascular Devices Company Type:
Clinical-stage medical device developer focused on structural heart therapies Were partnering with an [...]
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[...] emerging German Med Tech company developing a catheterbased Class III implant for structural heart repair. The device targets a major unmet need in minimally invasive heart valve therapy and is on track for pivotal trials. The company is now hiring a QA/ RA Manager to take ownership of its Quality and Regulatory function. This is a hightrust role, reporting directly to the Managing Director, and acting as the Quality Management Representative and Person Responsible for Regulatory Compliance. Quality Management Lead daytoday QMS operations (ISO13485:2016, 21CFR [. .. ]
Job am 06.11.2025 bei Jobleads gefunden
• Basel, Basel- Stadt
What you will be doing Participate in patient recruitment for international multicentre
trials, contribute to outpatient clinics, and gain increasing responsibility in the cath lab during valve procedures (TAVI, TEER, [...]
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[...] TMVR, etc. ) , based on technical competence Spend one day per week in the cath lab, gaining direct involvement in structural heart interventions. Fellows will learn advanced techniques such as preprocedural CT analysis using dedicated software Join Heart Team meetings three times per week, participate in clinical rounds and journal clubs, and contribute to patient management decisions at a consultant level. Engage in clinical research within the Cardiovascular Research Institute Basel (CRIB) . Fellows will receive mentorship in study design, data collection, analysis, manuscript preparation, and publication While not mandatory, fellows may opt to participate in oncall duties to gain additional experience in emergency situations Your profile Completion of core [. .. ]
Job am 08.10.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] präsentierst wissenschaftliche Daten, Studienergebnisse und medizinisches Hintergrundwissen. Du entwickelst Kommunikationsformate für den Austausch mit KOL und nimmst an relevanten nationalen und internationalen Kongressen teil. Du bist die [...]
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[...] Schnittstelle zwischen Fachabteilungen Clinical Trials, Produktmanagement und Außendienst und schulst wissenschaftliche Inhalte nach innen und außen. Du hast ein erfolgreich abgeschlossenes medizinisches oder naturwissenschaftliches Studium. Du hast bereits 3 Jahre Berufserfahrung im Bereich Medical Affairs oder in vergleichbaren Themenfeldern gesammelt. Du zeichnest Dich durch eine selbstständige und strukturierte Arbeitsweise aus, regelmäßige berufliche Reisen siehst Du [. .. ] Menschen ein neues Leben Aus Gründen der besseren Lesbarkeit wird in dieser Anzeige die männliche Form verwendet. Sie bezieht sich ausdrücklich auf alle Geschlechter (w/m/d) . IT (Senior) Consultant für Regulatory Affairs, Medical Affairs oder Drug Safety-Life Science (w m d) Medical Science Liaison Hämatologie (all genders) für die Region Bayern Medical Science Liaison Hematology (München/ Nürnberg) (Sr) Medical Science Liaison Rare Diseases/ Friedreich Ataxie (FA) (f/m/d) Medical Science Liaison (m/w/d) Onkologie-Gastrointestinale Tumore [. .. ]
Job am 03.07.2025 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Zürich Zuerich
Homeoffice möglich
For our customer located in Zurich/ Switzerland we are currently looking for a : Manager Regulatory Affairs (remote) (m/f/x) Remote:
Consultant needs to be based in Switzerland, but the HM [...]
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[...] is flexible when it comes to home office, there might be just a few days needed onsite. Travel: Requires approximately 10 travel Tasks Responsibilities Objectives: Responsible for supporting the regulatory activities related to the development, registration and life cycle management of [. .. ] and life cycle management for vaccine candidates in the region Ensures that all necessary applications are filed and maintained in compliance with applicable regulations. Responsible for regulatory oversight of assigned clinical trials conducted in the region. Provides regulatory oversight for assigned projects, focused on non-clinical and clinical aspects of drug development/ approval and associated regulations. Collaborates with all regulatory counterparts to ensure alignment and execution of the global regulatory strategy for the assigned projects. Passion for quality in all areas of [. .. ]
Job gestern bei Jobleads gefunden
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 and increased patient access to medicines, and accelerated regulatory approval. Informed decision-making reduced clinical trial burden Higher R D productivity Improved patient outcomes increased patient access to medicines Accelerated regulatory approval Certara is a global team that nurtures a diverse [. .. ] Responsibilities 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. Independent performance of analysis and modeling and development of reports with limited supervision. Comfortable in a client environment able to communicate with and collaborate with peer scientists. Developing ability to identify new business [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Senior Principal
Consultant (Medical) at Bio Talent, part of The IN Group Bio Talent are delighted to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, [...]
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[...] currently hiring for a Global Head of Pharmacovigilance. This is a strategic leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. The role will direct safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. It is central to ensuring safe, compliant, and successful oncology drug development and maximising patient safety from clinical trials to postmarketing surveillance. This position will report to the Chief Medical Officer and may work on a hybrid basis from the company office in Germany or remotely. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Frankfurt (Oder) , Brandenburg
Führungs-/ Leitungspositionen
[. .. ] clients and other internal departments, and applying advanced statistical methods to project work. Serve as a resource for the department, ensuring scientific integrity in the application of [...]
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[...] statistical methodology to clinical trials. Assist the Director in strategic planning and resource allocation for the department. Participate as senior statistician on major projects, including developing/ reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports. Assist the Director in proposal development, project allocations, budget projections, and client [. .. ] more at Essential Functions Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Oversees team with same expectations. Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company. Maintains knowledge and awareness of developments in Biostatistics and clinical trial methodology, and regulatory requirements that impact analyses. Represent clients at meetings with regulatory agencies or other regulatory meetings, may participate as a member [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
[. .. ] professionally. We recognize and value the importance of all people, the way we work, our drive for innovation and, most importantly, our patients. We are looking for [...]
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[...] a Senior Analyst Clinical Site Contracts, German Polish speaker to work 100 remotely in EU. The job is dedicated to one 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, maintenance, [. .. ] Pharma top 50. And we have an incredible pipeline of work. Expect exciting professional challenges in inspiring studies, but with time for your outside life. Responsibilities Negotiate and maintain Clinical Trials Agreements (CTA) , site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable contracts. As required, oversee CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols. Ensures compliance of contracts with Fair Market Value (FMV) principles and guidelines. Track contract progress, complete [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
• München, Bayern
Principal Sourcing Specialist Syneos Health Contract Specialist hybrid in Munich Syneos Health is a leading fully integrated biopharmaceutical solutions organization that accelerates customer success. It translates unique
clinical, medical [...]
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[...] affairs and commercial insights into outcomes to address modern market realities. The companys clinical development model places the customer and the patient at the centre of everything it does, continually simplifying work to make Syneos Health easier to work with and to work for. Whether you join us in [. .. ] to accelerate the delivery of therapies because we are passionate about changing lives. Job Responsibilities Administers all contract management processes, including coordination with relevant protocol, informed consent, institution, investigator, vendor, consultant, and customer agreement documents at a project level. May lead (with supervision) multicountry projects including negotiating and preparing contracts, budgets, and related documents for participation in industrysponsored clinical trials. Provides support to SSUL to agree on country template contract and budget. Produces sitespecific contracts from country template. Provides support in submissions for proposed contract and budget for site. Provides support in negotiating budget and contract with site via Site Contracts Service Centre and SSUL with Sponsor until resolution of [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
Expert Innovative Statistics Consultant
Beratungs-/ Consultingtätigkeiten
Job Description We are currently seeking an Expert Innovative Statistics
Consultant to join our Strategic Consulting Practice. This is an exceptional opportunity for a seasoned Biostatistician or strategic expert [...]
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[...] in clinical development to make a real-world impact by advising clients, shaping regulatory and market access strategies, and contributing to thought leadership in the industry. Lead high-value consulting engagements for pharmaceutical, biotech, and medical device clients. Provide strategic guidance on clinical development, regulatory pathways, and market access. Serve as a [. .. ] leaders. Qualifications Advanced degree (Masters required, Ph D preferred) in Biostatistics, Mathematics, or a related field; MBA, MD, or other advanced degrees are highly desirable. 1015+ years of experience in clinical trials, biostatistics, or health research. Deep understanding of biopharmaceutical R D processes and business strategy. Proven experience with regulatory strategy and engagement (FDA, EMA) . Strong leadership and clientfacing consulting experience. Entrepreneurial mindset, strategic thinker, and excellent communicator. Willingness to travel and engage directly with clients and stakeholders. Why Join Cytel? [. .. ]
Job am 31.08.2025 bei Jobleads gefunden
VP Pathology (m/f/d)
• Kassel, Hessen
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 27.08.2025 bei Jobleads gefunden
Director, Pharmacometrics
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] and the people that need them most. Innovation and creativity are highly valued, and everyone is given the opportunity for training and continuous development. Our portfolio spans [...]
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[...] the discovery, preclinical, clinical and post-marketing phases of drug development, working with 1, 200 commercial companies, 250 academic institutions, and numerous regulatory agencies. In the past 6 years, over 90 of companies that received new drug approvals by the FDA used our software or services. Our integrated and proprietary end-to-end platform [. .. ] 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, [. .. ]
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 Bayern (2 Jobs), Sachsen-Anhalt (2 Jobs) und Hessen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Consultant Jobs?
Clinical Trials Consultant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
