15 Jobs für Clinical Trials Consultant
Stellenangebote Clinical Trials Consultant Jobs
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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 [...]
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 gestern bei Jobleads gefunden
• 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, [. .. ] German and English is essential. An advanced ability to speak and read Polish is also preferred. Responsibilities Negotiate and maintain Clinical Trials Agreements (CTA) , site budgets, Confidential Disclosure Agreements, Consultant Agreements and other applicable contracts. 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. Ensure compliance of contracts with Fair Market Value (FMV) principles and guidelines. Track contract progress, complete required followups [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA
Consultant to support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality processes for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
GCP QA Consultant
Beratungs-/ Consultingtätigkeiten
[. .. ] message the job poster from Proclinical Staffing Connecting top-tier QA talent with groundbreaking life sciences opportunities Champion compliance and precisionhelp deliver lifechanging therapies. Proclinical is seeking a [...]
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[...] GCP QA Consultant to support quality assurance activities for oncologyfocused clinical trials. This role involves overseeing quality processes for phase 23 studies, ensuring compliance with ICHGCP and regulatory requirements, and managing riskbased quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote position, open to [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Wien
Freiberuflich
Get AI-powered advice on this job and more exclusive features. Direct message the job poster from EPM Scientific Vice President-Recruiting in the
Clinical Operations, Clinical Development and Medical Affairs space [...]
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[...] across Europe EPM Scientific is currently partnered with a CRO client running a project in Austria. They are urgently seeking an experienced Freelance CRA to support their expanding clinical operations team. Contract Conditions Start date: ASAP/ January Location: Remote, Austria Contract Type: Freelance/ Consultant-0.2 FTE Duration: 12 Months Language: German English preferred Project: Dermatology/ Paediatric Rare Disease Key Responsibilities Perform monitoring activities for clinical trials in compliance with ICH-GCP and local regulations. Ensure proper site management and maintain strong relationships with investigators and site staff. Review source documents and verify CRF data accuracy. Track study progress and ensure timely resolution of queries. Collaborate with project managers and clinical teams to ensure high-quality deliverables. [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Beratungs-/ Consultingtätigkeiten
[. .. ] among the first 25 applicants Direct message the job poster from R D Partners Empowering consultancies, biotech, and pharma companies to scale highperforming HTA/ RWE teams with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategic recruitment solutions. Consultant Shape the future of clinical trials by driving Patient Reported Outcomes strategies that meet global standards and deliver realworld impact. R D Partners is seeking a skilled PRO Consultant to provide expertise in Patient Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment with [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• 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 am 08.12.2025 bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Executive Director, Oncology Early
Clinical Development Lead Join to apply for the Executive Director, Oncology Early Clinical Development Lead role at GSK. GSK aims to positively impact the health of [...]
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[...] 2.5billion people by the end of the decade, focusing on vaccines and medicines that address patients needs with the highest probability of success. Position [. .. ] or Stevenage) , Switzerland (Zug) or Poland (Warsaw) . Responsibilities Accountable for the clinical development plans (CDPs) for a portfolio of earlyphase (Phase I/ II) clinical study protocols, including firstinhuman (FIH) trials, doseescalation studies, and proofofconcept (POC) studies. Steer the clinical benefitrisk balance of programs, delegating to and interfacing closely with appropriate physicians when needed. Drive endtoend clinical development strategy and alignment to target medicine profiles (TMP) and integrated evidence plans (IEP) , spanning trial design, execution, interpretation, and delivery of results. [. .. ] presentations, and manuscripts for accuracy and compliance. Lead preparation of clinical sections of regulatory filings (IND, study reports, NDA, annual reports, etc. ) . Provide clinical support for investigator and consultant meetings (e. g. , investigator meetings, advisory boards) . Present study results and translational insights to senior management, scientific advisory boards, regulatory agencies, and other stakeholders. Integrate input from research, clinical, medical, scientific, commercial, regulatory, and manufacturing disciplines to ensure alignment and execution of translational research initiatives. Build and maintain [. .. ]
Job am 05.12.2025 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 04.12.2025 bei Jobleads gefunden
Global Head of Pharmacovigilance
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 am 27.11.2025 bei Jobleads gefunden
Senior Research Consultant DACH (mfd)
• Wien
Beratungs-/ Consultingtätigkeiten
[. .. ] transparency in our recruitment process and weve created a blog to share what to expect during each step of our journey together : here Your mission as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Senior Research Consultant We are looking for a Senior Research Consultant (m/f/d) to join our Research Consulting this role you will be in charge of advising and coaching our clients throughout the entire market research process from finding the right methodology to interpreting the results for a multitude of different projects. [. .. ] read our privacy policy here. Learn more about us : Linked In Xing Kununu Instagram Required Experience : Senior IC Key Skills Spss, FDA Regulations, Data Collection, R, Regression Analysis, Clinical Trials, Research Experience, Statistical Software, Market Research, SAS, Data Analysis Skills, Wiki Systems Employment Type : Full Time Experience : years Vacancy : 1 #J-18808-Ljbffr 70719174 [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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, [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
Proclinical
GCP QA Consultant
• Berlin
Beratungs-/ Consultingtätigkeiten
Champion compliance and precision-help deliver life-changing therapies. Proclinical is seeking a GCP QA
Consultant to support quality assurance activities for oncology-focused
clinical trials. This role involves overseeing quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] processes for phase 2-3 studies, ensuring compliance with ICH-GCP and regulatory requirements, and managing risk-based quality plans. You will collaborate with internal teams and external partners to maintain high standards of clinical trial execution and inspection readiness. This is a fully remote [. .. ]
Job vor 5 Tagen bei Neuvoo.com gefunden
R D Partners
PRO Consultant
• Stuttgart
Beratungs-/ Consultingtätigkeiten
Shape the future of
clinical trials by driving Patient-Reported Outcomes strategies that meet global standards and deliver real-world impact. R D Partners is seeking a skilled PRO
Consultant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to provide expertise in Patient-Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment with strategic objectives and regulatory requirements. Please note that to be considered for this role you must have the right to work in this [. .. ]
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 15 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 Berlin (3 Jobs), Baden-Württemberg (2 Jobs) und Bayern (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Consultant Jobs?
Clinical Trials Consultant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
