20 Jobs für Clinical Drug Consultant
Stellenangebote Clinical Drug Consultant Jobs
Job vor 5 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job [...]
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[...] Description Summary Principal Consultant Regulatory Strategist brings scientific depth and regulatory foresight to product and business strategy anticipating regulatory and policy trends, shaping development paths, and enabling commercial advantage. This role is defined by influence: partnering with the rest of the regulatory strategy team, CMC, clinical strategy, clinical operations, quality, legal and commercial leaders to design pathways to market and lifecycle value, not merely to follow them. The Principal Consultant Regulatory Strategist is a senior scientific leader within the Regulatory Strategy team, reporting directly to the SVP Regulatory Strategy. The Principal Consultant Regulatory Strategy will contribute [. .. ] and scenario planning) to identify emerging regulatory, policy and scientific trends and translate these into actionable recommendations for clients and internal teams. Develop and lead global regulatory strategies for client drug development programs. Co-create integrated development strategies and regulatory roadmaps that align scientific design, clinical strategy, CMC and commercial when appropriate to support clients objectives. Explore alternative pathways that optimize use of Agency tools, programs to enhance the development journey and lifecycle value in particular for early development projects. Advise [. .. ]
Job am 26.01.2026 bei Jobleads gefunden
Head of Network Strategy and Post-Merger Integration (m/f/d)
• 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 [...]
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[...] 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 gestern bei Jobleads gefunden
Director, Clinical Development
• 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, [. .. ] The Role Responsible for developing strategy and plans for Phase 13 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 Phase13 Clinical Trials for the clinical development in accordance with Neurocrine SOPs and GCP guidance Develops and implements [. .. ] 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 3 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Are you an experienced CMC
Consultant? Do you have experience covering all quality related topics from pre-
clinical development to approved commercial products? If so, this could be the perfect opportunity [...]
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[...] for you We are recruiting for a CMC Consultant to join a leading Regulatory Consultancy business based in Munich on a permanent basis. Our client offers full flexibility to manage your own 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 [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Senior Product Manager, Germany (contract)
• Frankfurt, München, Berlin, Hesse, Bayern
[. .. ] problems, with a focus on allergy/ inflammation and oncology/ hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core [...]
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[...] focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success, 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 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 [. .. ] 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 28.02.2026 bei Jobleads gefunden
• Hamburg
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
Clinical Consultant (all genders) page is loaded # # Clinical Consultant (all genders) locations: Hamburgtime type: Full timeposted on: Posted Todayjob requisition id: 567514 # # # Job Title Clinical [...]
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[...] Consultant (all genders) # # # Job Description CVI Solutions Service Delivery ist Teil der Businessgroup Enterprise Informatics (EI) und als Service-[. .. ] require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/ Vets and maintains a drug-free workplace. #J-18808-Ljbffr 82181672 [. .. ]
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 [...]
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[...] 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 22.02.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Director, Pharmacometrics Overview: About Certara Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional
drug discovery and [...]
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[...] development. Our clients include more than 2, 400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries. Our goal is to enable the life sciences industrys use of data, modeling, and analytics to make better decisions across the various phases of discovery and drug development. Our software [. .. ] 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 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 [. .. ]
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 [...]
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[...] 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 [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
Advanced Resource Managers
Regulatory CMC Consultant
• München, Bayern
Beratungs-/ Consultingtätigkeiten
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 [...]
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[...] CMC work-packages and documentation are phase appropriate, meet regulatory expectations and enable approval of regulatory submissions. Preparation of quality sections for MAA and BLA/ NDA as well as for IMPD [. .. ] 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) . Disclaimer This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource [. .. ]
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 [...]
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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 [. .. ] 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 Strong analytical and problem-solving skills Excellent communication skills (written and verbal) Leadership and mentoring capabilities Nice to Have Experience leading small teams or study teams Exposure to global client environments [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Tech Biz Global GmbH
• 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 [. .. ] 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 Strong analytical and problem-solving skills Excellent communication skills (written and verbal) Leadership and mentoring capabilities Nice to Have Experience leading small teams or study teams Exposure to global client environments [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Infosys Consulting- Europe
Sr. Principal Consultant, Regulatory Strategy and Advisory
• Munich, Bavaria Muenchen
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 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 [. .. ] experience within the life-science industry Expert in a broad range of complex statistical methods that apply to Phase 2-3 clinical trials Expert in strategically collaborating with clinical and drug development experts Experience in serving as statistical lead for regulatory submissions, including preparation of submission datasets, e CTD support, meeting with regulatory teams, and responding to regulatory queries In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong working knowledge [. .. ]
Job am 10.03.2026 bei Neuvoo gefunden
KBR
Special Operations Licensed Clinical Social Worker (Stuttgart, Germany)
• Stuttgart, Baden- Württemberg
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 [...]
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[...] dreamers; 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 [. .. ] behavioral 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, couples 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 08.03.2026 bei Neuvoo gefunden
Immunic AG
• Gräfelfing, Bavaria
Beratungs-/ Consultingtätigkeiten
Your mission We are looking for a
Consultant (m/f/x) to support our Medical Writing activities in connection with a NDA submission. This assignment can be done remotely from the [...]
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[...] EU, UK or US (preferably East Coast) , and includes: Collaboration with our internal team members on our NDA preparation by writing clinical modules (AMDE, DDI, FE/ FA, BE, TQT, COC) Support our clinical pharmacology experts as lead medical writer Provide project management for clinical pharmacology modules Interact with non-clinical pharmacology experts, internal and external reviewers Time commitment: 32h/ week Project duration: appr. 12 months Your profile Solid experience in writing NDA/ [. .. ] modules and clinical pharmacology/ Phase 1 study strictly required Medical or science degree with substantial medical/ regulatory writing experience in Biotech or Pharma Native-level English proficiency Strong understanding of drug development processes, regulatory interactions, and applicable global regulations (especially US FDA) Proficient with relevant software tools, style guides, and document formatting standards Excellent project management incl. leading cross-functional, international teams Collaborative and proactive approach, and solution-focused mindset About us Immunic Therapeutics is a dynamic biotechnology company with a [. .. ]
Job am 07.03.2026 bei Neuvoo gefunden
Immunic AG
Senior Consultant (m/f/x) - Medical Writing, Clinical NDA modules
• Gräfelfing, Bavaria
Beratungs-/ Consultingtätigkeiten
Your mission We are looking for a
Consultant (m/f/x) to support our Medical Writing activities in connection with a NDA submission. This assignment can be done remotely from the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] EU, UK or US (preferably East Coast) , and includes: Collaboration with our internal team members on our NDA preparation by writing clinical modules (efficacy and safety) Support our medical experts as lead medical writer Provide project management for NDA submission modules 5 and 2 (clinical sections) Interact with internal and external reviewers Time commitment: 40 h/ week Project duration: appr. 12 months, extension possible Your profile Solid experience in writing NDA/ MAA/ e CTD clinical modules strictly required Medical or science degree with substantial medical/ regulatory writing experience in Biotech or Pharma Native-level English proficiency Strong understanding of drug development processes, regulatory interactions, and applicable global regulations (especially US FDA) Proficient with relevant software tools, style guides, and document formatting standards Excellent project management incl. leading cross-functional, international teams Collaborative and proactive approach, and solution-focused mindset About us Immunic Therapeutics is a dynamic biotechnology company with a [. .. ]
Job am 02.03.2026 bei Neuvoo gefunden
KBR
• Stuttgart, Baden- Württemberg
Title: Special Operations Licensed
Clinical Social Worker (SOCAFRICA, Kelley Barracks-Stuttgart, Germany) THIS POSITION OFFERS RELOCATION. Belong. Connect. Grow. with KBR KBR is a company of innovators, thinkers, creators, explorers, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] volunteers, and dreamers; but we all share one goal: to improve the world responsibly and safely. We maintain a highly qualified workforce to help care [. .. ] behavioral 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, couples 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 20.10.2025 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 [...]
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[...] 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 66556414 [. .. ]
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 20 offene Stellenanzeigen für Clinical Drug Consultant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Consultant Jobs?
Aktuell suchen 8 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:
- Tech Biz Global GmbH (2 Jobs)
- KBR (2 Jobs)
- Immunic AG (2 Jobs)
- Advanced Resource Managers (1 Job)
- Infosys Consulting- Europe (1 Job)
- IQVIA (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 (8 Jobs), Berlin (2 Jobs) und Hessen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Consultant Jobs?
Clinical Drug Consultant Jobs gehören zum Berufsfeld Pharmazie.
