13 Jobs für Clinical Drug Consultant
Stellenangebote Clinical Drug Consultant Jobs
Job am 26.01.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] of Network Strategy and Post-Merger Integration. Adragos Pharma is a reliable Contract Development and Manufacturing Organization (CDMO) headquartered in Munich, Germany. We provide comprehensive development and manufacturing [...]
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[...] services for drug products, including sterile and non-sterile liquids, solids, and semi-solids. Our expertise also covers biologicals, orphan 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 [. .. ] 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
Discovery Life Sciences is a global market leader in biospecimen solutions and laboratory services, offering an extensive range of products and services to support
drug discovery and development. With a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] network of laboratories and offices across the United States and internationally, we are committed to advancing scientific research and improving health care outcomes. We are dedicated to accelerating the discovery and development of new therapies and diagnostics by providing the highest quality biospecimens, in vitro [. .. ] 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 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 [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Veeva Systems
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] and consulting working together. We expect significant growth in Business Consulting as we look towards 2030, and are looking for great people to make it happen. The [...]
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[...] Role As a Consultant in our R D Business Consulting practice, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI. You will focus on reshaping operating models, driving organizational change, and measuring tangible business value. R D Business Consulting supports biopharma, medtech, animal and consumer health customers with solving business problems across the R D value chain but also specifically within Clinical, Pharmacovigilance and Regulatory domains. You will be part of a global team delivering meaningful and high-impact projects with a variety of organisations from Top 20 Pharma to small/ mid-sized organisations. What Youll Do Lead project workstreams from end-to-end, ensuring the high-quality design and delivery of [. .. ] business development and internal IP creation Requirements Experience: 3+ years in Life Sciences Consulting (Business or Management Consulting preferred) Domain Knowledge: Proven expertise in Clinical Data/ Operations, Regulatory or Pharmacovigilance/ Drug Safety Analytical Rigor: A strong mindset for both quantitative and qualitative reasoning Communication: Ability to articulate complex ideas clearly to senior stakeholders Education: Bachelors degree or higher Not a perfect match yet? If you have 35 years of life sciences experience, a recent advanced degree, or a military background, Master [. .. ]
Job am 08.04.2026 bei Jooble gefunden
KBR
• Region Stuttgart, Württemberg; Regierungsbezirk Stuttgart; Württemberg Stuttgart, DE
Title: Special Operations Licensed
Clinical Social Worker (Stuttgart, Germany) THIS POSITION OFFERS RELOCATION. Belong. Connect. Grow. with KBR KBR is a company of innovators, thinkers, creators, explorers, volunteers, and dreamers; [...]
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[...] but we all share one goal: to improve the world responsibly and safely. We maintain a highly qualified workforce to help care for service people [. .. ] assessment, and evidenced-based therapies, in the evaluation, diagnosis, and treatment of psychological and neuropsychological disorders using the following skills: individual, family and group psychotherapy, couple s therapy, alcohol and drug treatment evaluations. Essential Duties Responsibilities: Engage all quality improvement and staff meetings, conferences Conduct applied research and clinical investigations in clinical/ behavioral health/ organizational social work. Consult with medical personnel, legal authorities, military commanders and school districts as required. Maintain accurate medical records of all patients seen and produces reports [. .. ] maintain accurate and current notes in the electronic medical records of all patients contacted for review by the managing physician; Routinely staffs difficult cases with the referring provider, behavioral health consultant and/or psychiatry consultant; and Performs case management functions. Required Education/ Experience/ Skills/ Training: Position requires U. S. Citizenship. All POTFF positions require a Do D Secret or Top Secret Clearance or the ability to obtain one. Master of Social Work (M. S. W. ) or equivalent (MSSW, MSSA) degree from [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Infosys Consulting- Europe
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Beratungs-/ Consultingtätigkeiten
[. .. ] and agile delivery experienced Role Summary, Core Expectations In depth knowledge of Pharma Regulatory Operations and Regulatory IT Systems aligned to core Functional and Technical competencies Expert [...]
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[...] in Regulatory and Clinical area with ability to drive futuristic IT solutions and experience in client facing and agency thought leadership. Understanding and knowledge of processes related to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific regulatory requirements keenly aware of industry trends, needs and business requirements [. .. ] outcomes Technical Credentials: Should have masters degree in a Life Science, Medical or Related discipline. Masters in Business Administration would be an added advantage. Minimum 12-15 years experience in Drug development, Regulatory, Clinical Operation and Medical Devices. Deep understanding of RIM systems i. e. , Veeva Vault, PARAXEL/ LIQUENT In Sight, CSC Regulatory Tracker, Aris Global Register, Open Text, Share Point, Documentum, First Doc/ First Point, Next Docs, CARA, Extedo e CTD Manager, Trackwise, or other regulatory information management systems Submission [. .. ]
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: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 statistical analyses for projects involving COA/ PRO data. You will contribute across analysis planning, execution, interpretation, reporting, and client communication, helping deliver evidence that is scientifically sound, regulatory-relevant, and clearly communicated. Key Responsibilities Lead the quantitative analysis [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Are you an experienced Senior Regulatory CMC
Consultant? Do you have hands-on CMC development experience in the pre-approval phase? Do you have IMPd/IND authoring experience? If so, this could [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] be the role for you We are recruiting for a Senior Regulatory CMC Consultant to join a leading Regulatory Consultancy business based in Munich on a [. .. ] workload within a professional and friendly working environment that is truly unique. The successful candidate will become the quality expert in our clients team, providing knowledge on broad range of drug substances from small molecules to synthetic oligonucleotides to biologicals, and drug products from solid orals to sterile solutions to nanoparticulate formulations. Responsibilities Provide advice to clients on quality aspects of drug development and regulatory requirements, in close collaboration with cross-functional experts from the team. Ensure that the content of [. .. ] IMPD, BLA/ NDA/ MAA) . Excellent communication and negotiation skills in English. German language skills are a plus. Experience with CMC and regulatory requirements for all development stages, from pre-clinical to Phase III or commercial. Highly motivated team player with strong interpersonal abilities. Sound knowledge of Microsoft Office applications. Willingness to travel moderately (Meetings with clients, agencies or CMOs) . #J-18808-Ljbffr 90654491 [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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, [. .. ] Role: Responsible for developing strategy and plans for Phase 1-3 clinical studies while working with a multidisciplinary team (R D project teams, clinical project managers, statisticians, data management, regulatory, drug safety) . As needed, 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 Phase 1-3 Clinical Trials for the clinical development in accordance with Neurocrine SOPs and GCP guidance [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 5 years of experience. Strong experience with Oncology TA. Strong oral and written communications 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 [. .. ]
Job am 05.04.2026 bei Jobleads gefunden
• Mannheim, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] development of pen and autoinjectors, pre-filled syringes, and other innovative delivery devices. Drive End-to-End (E2E) Collaboration: Build and maintain influential relationships across Industrialization, Regulatory, Quality, Operations, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical teams to ensure seamless device integration from early-stage to commercial launch. Architect Robust Product Platforms: Design and deliver diverse drug delivery technologies, including on body wearables, intraocular systems and smart devices, while exploring emerging areas like pulmonary delivery. Optimize Industrialization and Delivery: Oversee design verification and ensuring designs are optimized for large-scale manufacturing and robust industrial performance. Cultivate Strategic Partnerships: Manage and guide CDMOs and external suppliers, ensuring they [. .. ] in a diverse global environment. Effective Communicator: You possess exceptional interpersonal and presentation skills in English (German proficiency is a plus) , with the ability to serve as a primary consultant to top-level leadership. Ready to bring your unique qualities to Roche and make an impact? Apply now and join us in our mission to shape the future of healthcare. Qui nous sommes Un avenir plus sain nous pousse innover. Ensemble, plus de 100 000 employs travers le monde sont [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
Biopharma Strategy Consultant (PhD-entry level position)
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] and Consultants in an open team environment, primarily by conducting qualitative and quantitative analyses to help shape the final recommendation for our clients. This is usually focused [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] around scientific and clinical data but often includes business, industry and market landscape analyses. In addition, you will contribute in preparing the final presentation material and will gain direct exposure to our clients through involvement from Day 1 in working team as well as executive meetings. Requirements Ph D degree in a relevant biomedical or [. .. ] now button. Further questions? Feel free to reach out to About us Our work is focused on various aspects of R D strategy, sciencedriven screens to identify the most suitable drug inlicensing opportunities to fit every individual clients capabilities and goals, as well as reviewing scientific and clinical data, experiments, statistical assumptions, and thus power, estimating its probability of success. All this put into context generates key insights for our clients. #J-18808-Ljbffr 82191132 [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
National Market Access Lead (m/w/d)
• München, Bayern
Führungs-/ Leitungspositionen
Sabbaticals
[. .. ] will work cross-functionally and globally to embed sustainable access approaches across the product lifecycle. You will shape national HTA submissions, develop evidence-driven payer value propositions, and translate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] complex clinical and economic data into strategic outcomes. This role will also offer exciting proximity to Modernas digital ambitions, with opportunities to work closely with real-world data and explore synergies with generative AI tools in evidence generation and access storytelling. Heres What Youll Do Your key responsibilities will be: Lead the [. .. ] real-world datasets into compelling payer value stories and clear evidence frameworks. Coordinate cross-functional teams (Market Access, HEOR, Medical, Commercial, external experts) for strategy execution. Act as an internal consultant to align local market insights with global product and platform plans. The key Moderna Mindsets youll need to succeed in the role: We digitize everywhere possible using the power of code to maximize our impact on patients. In this role, the ability to interface with large datasets, claims-based systems, [. .. ] join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work #J-18808-Ljbffr 72357105 [. .. ]
Neu Job vor 3 Std. bei Job-Consult gefunden
PhD- Jobs. NET
Specialist Adult Psychiatry
• Schweden/ sonstiges/ Europa
[. .. ] supervision of younger colleagues is included as a natural part of the work and participation in the units medical development specialists perform the most physician specific tasks [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] such as diagnostics drug treatment and the establishment of a care treatment plan together with the team on the other hand psychotherapies are conducted by psychotherapists with other basic professionals dutywork is included in the service both daily and evening night duties you also need knowledge to replace your staff when vacation illness etc [. .. ] participating in the development of this we also wish you to have an interest in adhd treatment and substitution treatment for opiate addiction number of vacancies education specialist education psychiatry clinical experience what kind of treatments patients do you expect the doctor to have experience with years of experience all of the vacancies involve working with most of the psychiatric diagnoses why a broad background is a plus special knowledge and skills or special interests that are important to the job [. .. ] as a specialist your role will be to back up the residents when you get a delegation to deal with emergency care issues which usually happens when you get a consultant employment your duty will instead be a backup doctor to apply please send your cv mentioning reference lr at info phd jobs net contact person vitaly pryadka tel web http www phd jobs net gesundheits sozialwesen sonstiges europa medizin pharma sozialwesen vollzeit 91235084 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Consultant pro Jahr?
Als Clinical Drug Consultant verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 13 offene Stellenanzeigen für Clinical Drug Consultant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Consultant Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Clinical Drug Consultant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Drug Consultant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Drug Consultant Stellenangebote:
- Veeva Systems (1 Job)
- KBR (1 Job)
- Infosys Consulting- Europe (1 Job)
- PhD- Jobs. NET (1 Job)
In welchen Bundesländern werden die meisten Clinical Drug Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Consultant Jobs werden derzeit in Bayern (4 Jobs), Baden-Württemberg (2 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Consultant Jobs?
Clinical Drug Consultant Jobs gehören zum Berufsfeld Pharmazie.
