57 Jobs für Clinical Drug Specialist
Stellenangebote Clinical Drug Specialist Jobs
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
25108671 Global Senior Project
Specialist (Sponsor Dedicated) Germany Syneos Health is a leading fullyintegrated life sciences services organization built to accelerate customer success. We partner with innovators at every point [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Job Responsibilities Setup, maintain and/or close out project files and study information (e. g. , regulatory documents, Trial Master [. .. ]
Job am 31.05.2026 bei Mindmatch.ai gefunden
IQVIA
Global Clinical Contracts Lead
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] training and experience. Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and then communicate these with study [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] training and experience. Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and then communicate these with study [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
Contract Negotiator
• AT- 9 Wien
[. .. ] stakeholders, and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] negotiator. Good negotiating and communication skills with the ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of the drug development process. Knowledge of and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and the companys Corporate Standards. Strong understanding of particular sponsor or stakeholder needs and the ability to share this knowledge effectively with others. Ability to utilize metrics and communicate these [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report contracting performance metrics and out of scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and [. .. ] site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Good understanding of clinical trial contract management. Fluent in English and German language IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical [. .. ]
Job am 25.05.2026 bei Jobleads gefunden
Medico Capoclinica/ Senior Staff Physician
• Bellinzona, Tessin
[. .. ] caring for more than 41, 000 patients a year and providing more than 600, 000 ambulatory consultations. To complete the team at the Oncological Institute of Southern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Switzerland (IOSI) Bellinzona, Clinical Research Unit and Phase 1 Program, we are looking for a Senior Staff Physician (80100) . Medico Capoclinica/ Senior Staff Physician (80100) The Oncology Institute of Southern Switzerland is one of the largest clinical research centers in Switzerland. Our three main areas of clinical research comprise new drug development, lymphoproliferative diseases and prostate cancer. Other important areas of development include gynecological, breast, lung, skin and gastrointestinal cancer. The IOSI has a dedicated Phase 1 Unit where early phase clinical trials, including firstinhuman, are conducted. We have an excellent history of collaborating with nonforprofit academic organizations and the pharmaceutical [. .. ] innovative translational and clinical research programs. Clinical activities within a selected disease group can also be considered, aligned with the candidates areas of expertise. Essential Requirements Medical degree and completed specialist training in Medical Oncology. For candidates holding foreign qualifications, recognition by the Swiss Federal Commission for Medical Professions (MEBEKO) is mandatory. The qualification must be equivalent to the Swiss standard; recognition may be obtained after acceptance of the position. Registration in Med Reg is also required, including proof of proficiency [. .. ]
Job am 24.05.2026 bei Jobleads gefunden
• Bellinzona, Tessin
EOC-Ente Ospedaliero Cantonale in Bellinzona, Switzerland seeks a Senior Staff Physician specializing in
drug development and early-phase
clinical trials in oncology. The candidate will engage in clinical activities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aligned with their expertise and support the educational efforts of the institute. Qualifications include a medical degree, specialist training in Medical Oncology, and experience in early-phase clinical trials. Proficiency in both Italian and English is essential. An entry date is flexible, with the position expected to start from September 2026. #J-18808-Ljbffr 92485437 [. .. ]
Job am 24.05.2026 bei Jobleads gefunden
Medico Capoclinica/ Senior Staff Physician
• Bellinzona, Tessin
About the IOSI The Oncology Institute of Southern Switzerland (IOSI) is one of the largest
clinical research centers in Switzerland. Our three main areas of clinical research comprise new [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] drug development, lymphoproliferative diseases and prostate cancer. The IOSI has a dedicated Phase 1 Unit where early phase clinical trials, including firstinhuman, are conducted. We collaborate with academic organisations and the pharmaceutical industry, including the Institute of Oncology Research, the Institute of Biochemical Research and the Swiss Cancer Institute. Position Overview [. .. ] phase clinical trials in oncology. Key Responsibilities Clinical activities within a selected disease group can also be considered, aligned with the candidates areas of expertise. Qualifications Medical degree and completed specialist training in Medical Oncology. For candidates holding foreign qualifications, recognition by the Swiss Federal Commission for Medical Professions (MEBEKO) is mandatory. The qualification must be equivalent to the Swiss standard; however, recognition may be obtained after acceptance of the position. Registration in Med Reg is also required, including proof of [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Global Senior Project Specialist (Sponsor Dedicated) Germany
• Wien
25108671 Global Senior Project
Specialist (Sponsor Dedicated) Germany Syneos Health is a leading fullyintegrated life sciences services organization built to accelerate customer success. We partner with innovators at every [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Job Responsibilities Setup, maintain and/or close out project files and study information (e. g. , regulatory documents, Trial Master [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Clinical Supplies Quality Auditor (GMP Release)
• Luzern
nemensis ag in Luzern, Switzerland, is seeking a dedicated
Specialist Clinical Supplies Quality to ensure GMP-compliant processes in clinical
drug supply. The ideal candidate holds a relevant university degree [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and has 2-3 years of experience in a GMP-regulated setting. Responsibilities include batch record review, inspection of packaging components, and regulatory review, all while maintaining rigorous quality standards. This role offers an opportunity to work in a dynamic team [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Ingelheim am Rhein, Rheinland- Pfalz
[. .. ] at the forefront of scientific storytelling and insights integration, translating deep scientific knowledge into strategic actions that resonate across internal teams and external experts. Collaborating closely with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the innovation and clinical development teams, focus markets, regional teams, and crossfunctional global stakeholders, you will ensure alignment, impact, and excellence in medical affairs. Tasks Responsibilities Lead the development and execution of globally aligned medical strategies for the Obesity and Liver Health pipeline, ensuring adaptation to evolving scientific, regulatory, and market dynamics Cocreate integrated [. .. ] integrate actionable insights into strategic decisions Build globallocal Medical Affairs collaborations to ensure knowledge transfer, launch readiness, and regional alignment Requirements Medical Doctor (e. g. , endocrinologist, internal medicine, obesity specialist, primary care physician) with a specialty in obesity medicine and experience in Obesity and Liver Health Longterm experience in the pharmaceutical industry, including several years in Medical Affairs as a Medical Advisor or Medical Manager in a global or international role Deep understanding of drug development, clinical trial design, data analysis, and interpretation, with expertise in introducing new medicines or expanding indications at a global level (e. g. , Obesity, Liver, or Cardiometabolic Health) Strategic thinker with strong crossfunctional collaboration skills, a clear understanding of medicomarketing processes, and the ability to lead impactful crossregional medical [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Quality Auditor (a) 100
• Luzern
Assignment Period 03.08.2026 31.07.2027, with option for extension About Our Client For our client, a globally active pharmaceutical company with a strong focus on
clinical research and
drug [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, we are looking for a dedicated Specialist Clinical Supplies Quality (f/m/d) . The organisation is renowned for its rigorous quality standards, innovative pipeline, and a collaborative culture that places patient safety at the heart of every decision. Responsibilities GM Pcompliant batch record review and formal release of clinical finished goods Incoming inspection and release of [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] Regional Director, Enterprise Client Success (RDECS) role manages our customers adoption and success utilizing the Synapse software application portfolio. This role requires an extensive background in enterprise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] imaging and firsthand clinical and or operational experience working in imaging departments. The RDECS will be responsible for the post implementation optimization strategy for our largest and most strategic enterprise imaging customers within a specific region. Additionally, this role requires strong executive engagement skills with demonstrated ability to effectively communicate complex technical concepts, strategy, [. .. ] collaboration with product management. This role will participate in all Synapse customer user group activity. Sales Business Development This role will work closely with regional sales leadership and regional product specialist to drive the expansion of Synapse products within their client sites. Support major trade shows, and contribute to industry panels, blogs, and publications. Work closely to develop customer thought leadership and Synapse product support in each market segment, i. e. , Academic, Pediatric, Mammography and Outpatient. Marketing Sponsor and guide [. .. ] trade shows, and contribute to industry panels, blogs, and publications. Support organizational transition and the near elimination of private data centers. Other Comply with all applicable U. S. Food and Drug Administration (U. S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. Qualifications Education Experience Radiology or Cardiology technologist degree, bachelors degree, or equivalent work experience. 10+ years of progressive leadership experience in radiology and or cardiology business operations, informatics system [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Clinical Pharmacist-Yanbu-
• Gössendorf, Steiermark
[. .. ] Part Time/ Full Time: Full Time About the Role To be responsible for the pharmaceutical care management for assigned clinic (s) by ensuring excellence in service delivery [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] according to Diaverum clinical governance five core practices (clinical standards, medical standards, performance measurement, education, and scientific research) . To plan, coordinate, deliver, and evaluate the pharmaceutical care service, be responsible provision of drug therapy for purpose of achieving definite therapeutic outcome that improve the patient quality of life, wellbeing and health promotion (educational activities) , Pharmaceutical supply management, scientific research and preventive care services to provide life enhancing renal care. Key Responsibilities Definition of Reporting Lines The pharmacist is accountable to the Direct [. .. ] of pharmaceutical team as applicable. Participate in self and others education, training and development including assigned pharmacist interns as applicable. Qualifications Education Bachelors degree in Doctor of Pharmacy Certified Pharmacist Specialist by the Saudi Commission for Health Specialties (SCFHS) Experience Fresh Graduate, 1-2 years clinical dietetics experience in a clinical setting or hospital is favorable. Experience in clinical specialty favorable (renal, diabetes, hypertension) Languages Fluent in Arabic and English (spoken and written) IT Skills Computer operating experience and MS Office [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
[. .. ] and University Hospital are part of the University of Excellence Tübingen. They provide medical services at the highest level and cover the entire spectrum of modern medicine, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] research, teaching and clinical care. The Faculty of Medicine at the University of Tübingen invites applications for a position at the University Clinic for Medicine, Internal Medicine VIII: Medical Oncology and Pneumology and with integration into the Cluster of Excellence Image Guided and Functionally Instructed Tumor Therapies (i FIT) as a Professor (W3) in Functional [. .. ] or similar methods. In collaboration with research groups within the i FIT Cluster of Excellence, particularly the Professorship for Cellular Immunotherapies in Cancer as well as Tü CAD2 (Tübingen Center for Academic Drug Discovery and Development) , the successful candidate will also coordinate translational projects aimed at developing new molecular therapeutics against identified targets. The successful candidate is moreover expected to translate therapeutic concepts developed preclinically within the context of the i FIT Cluster of Excellence into clinical practice through investigatorinitiated trials (IITs) . [. .. ] of and for the duration of funding by the Cluster of Excellence, the teaching load may be reduced appropriately. Prerequisites for employment are a license to practice medicine and the specialist qualification in internal medicine or an international equivalent which is recognized as equivalent by the Baden Württemberg Medical Association (Landesärztekammer) . The specialist qualification in internal medicine and hematology/ oncology or internal medicine and pneumology is desirable. Also required are postdoctoral qualifications and teaching experience equivalent to the requirements of [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Principal/ Senior Scientist, Biological Process Development
• München, Bayern
The Senior Scientist, Biological Process Development is a highly skilled and collaborative team member responsible for designing, executing, and interpreting experiments that advance
drug substance process development for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] companys live biotherapeutic product (LBP) pipeline. This role spans both upstream and downstream processing activities for drug substance-from fermentation optimization and scale-up through harvest, concentration, lyophilization, and preparation for drug product manufacturing. In addition to strong bench science capabilities, the Senior Scientist will play an active role in coordinating technical activities with external contract development and manufacturing organizations (CDMOs) and specialist vendors, serving as an informed day-to-day liaison between internal development programs and the external partner network. KEY RESPONSIBILITIES Process Development Design and execute fermentation development experiments using bench-top and pilot-scale bioreactors, including operation of anaerobic culture systems appropriate for LBP organisms. Optimize culture media, seed train [. .. ] audiences including non-technical stakeholders. Provide day-to-day technical guidance and mentorship to scientists and research associates within the process development group. Collaborate closely with Analytical Development, CMC, Quality, Clinical, and Regulatory to ensure internal and external development activities are aligned and on schedule. Contribute to a culture of scientific rigor, continuous improvement, and open knowledge sharing across the company. QUALIFICATIONS Required Ph. D. in Microbiology, Biochemical Engineering, Bioprocess Engineering, Pharmaceutical Sciences, or a closely related discipline with 3+ years [. .. ]
Job am 05.06.2026 bei Jobleads gefunden
Position Overview The Associate
Clinical Specialist independently provides customer support of Fujifilms ES equipment in the Endoscopy department and/or specified departments. This role manages all relevant equipment and uses its [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] own judgement and decision-making skills to provide troubleshooting and training for the proper handling of our equipment. This position provides on-site, hands-on [. .. ] integration into a future database application. Attend local, regional, and national trade shows as requested. Adhere to all safety policies and procedures. Comply with all applicable U. S. Food and Drug Administration (U. S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. Qualifications High School Diploma or equivalent is required. Bachelors degree in business, marketing or related quantitative disciplines preferred. Minimum of 2 years of field sales or clinical experience desired. [. .. ]
Job am 03.06.2026 bei Jobleads gefunden
Director, Computational Pathology Biomarker Lead (Oncology/ Bio Pharma) (m/f/d)
• München, Bayern
Führungs-/ Leitungspositionen
Director, Computational Pathology Biomarker Lead (Oncology/ Bio Pharma) (m/f/d) Do you thrive at the intersection of AI innovation and
clinical translation? Do you have expertise in, and a passion [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for leading cross functional teams to drive innovation? Would you like to apply your expertise to impact the Oncology and/or Bio Pharma strategic vision in a company that follows the science and turns ideas into life changing medicines? Then Astra [. .. ] In this position you will work with a multi-disciplinary team to pioneer AI-enabled computational pathology and multi-modal biomarkers that fundamentally change how we approach patient selection and drug development, aiming to improve clinical outcomes. You will have the opportunity to impact an industry-leading portfolio of targeted therapy programs from inception through to life cycle management for marketed drugs. This role is based at our Munch, Germany office. ABOUT ASTRAZENECA Astra Zeneca is a global, science-led, patient-[. .. ] pathways across Oncology and/or Bio Pharmaceuticals programs. Proven communication, presentation, and influencing skills at senior leadership levels with ability to articulate AI value proposition and implementation strategies to both specialist and non-specialist audiences. Outstanding analytical, research, and organizational skills with excellent problem-solving capabilities, clear understanding of the balance between innovation, smart risk-taking, fit-for-purpose solutions, and timely project delivery, and track record of consistent delivery and impact on drug development programs through AI innovation and successful [. .. ]
Job am 02.06.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
Director, Team Lead, Computational Pathology Biomarker Development (Oncology/ Bio Pharmaceuticals) (m/f/d) Do you thrive at the intersection of AI innovation and
clinical translation? Do you have expertise in, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a passion for leading cross functional teams to drive innovation? Would you like to apply your expertise to impact the Oncology and/or Bio Pharma strategic vision in a company that follows the science and turns ideas into life changing medicines? Then Astra [. .. ] In this position you will work with a multi-disciplinary team to pioneer AI-enabled computational pathology and multi-modal biomarkers that fundamentally change how we approach patient selection and drug development, aiming to improve clinical. You will have the opportunity to impact an industry-leading portfolio of diverse therapeutic programs from inception through to life cycle management for marketed drugs. This role is based at our Munch, Germany office. ABOUT ASTRAZENECA Astra Zeneca is a global, science-led, patient-focused [. .. ] pathways across Oncology and/or Bio Pharmaceuticals programs. Proven communication, presentation, and influencing skills at senior leadership levels with ability to articulate AI value proposition and implementation strategies to both specialist and non-specialist audiences. Outstanding analytical, research, and organizational skills with excellent problem-solving capabilities, clear understanding of the balance between innovation, smart risk-taking, fit-for-purpose solutions, and timely project delivery, and track record of consistent delivery and impact on drug development programs through AI innovation and successful [. .. ]
Job am 02.06.2026 bei Jobleads gefunden
Senior Scientist (m/f/d) , Computational Pathology Biomarker Lead (Oncology)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] team operates in a demanding, fast-paced environment where excellent collaboration, clear communication and precise organization are critical. BUSINESS AREA Astra Zenecas Enterprise AI organization is shaping the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] future of drug development with an integrated AI engine that connects data, technology, and expertise to accelerate breakthroughs. In Computational Pathology and Biomarkers, we deliver AI-driven solutions for patient selection, biomarker development, and clinical decisions on a scale. We collaborate across the organization to reuse capabilities and scale innovation globally measuring success by adoption, impact, and measurable outcomes across therapeutic areas and regions. Do you thrive at the intersection of AI innovation and clinical translation? Do you bring expertise in leading cross-functional teams [. .. ] collaboration and influencing skills, with the ability to work effectively in cross-functional, fast-paced environments. Excellent scientific communication skills, with the ability to present complex data clearly to both specialist and non-specialist audiences. Outstanding analytical, organizational, and problem-solving capabilities. Ability to prioritize effectively, remain highly productive, and balance innovation with timely project delivery in a dynamic environment. Demonstrated success contributing to interdisciplinary, cross-functional projects. Desirable Experience in the pharmaceutical or biotechnology industry, particularly in translational medicine or [. .. ]
Job am 31.05.2026 bei Jobleads gefunden
Global Clinical Contracts Lead
• Wien
Führungs-/ Leitungspositionen
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] training and experience. Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and then communicate these with study [. .. ]
Job am 29.05.2026 bei Jobleads gefunden
Senior Scientist (m/f/d) , Computational Pathology Biomarker Lead (Oncology)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] team operates in a demanding, fast-paced environment where excellent collaboration, clear communication and precise organization are critical. BUSINESS AREA Astra Zenecas Enterprise AI organization is shaping the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] future of drug development with an integrated AI engine that connects data, technology, and expertise to accelerate breakthroughs. In Computational Pathology and Biomarkers, we deliver AI-driven solutions for patient selection, biomarker development, and clinical decisions on a scale. We collaborate across the organization to reuse capabilities and scale innovation globally measuring success by adoption, impact, and measurable outcomes across therapeutic areas and regions. Do you thrive at the intersection of AI innovation and clinical translation? Do you bring expertise in leading cross-functional teams [. .. ] collaboration and influencing skills, with the ability to work effectively in cross-functional, fast-paced environments. Excellent scientific communication skills, with the ability to present complex data clearly to both specialist and non-specialist audiences. Outstanding analytical, organizational, and problem-solving capabilities. Ability to prioritize effectively, remain highly productive, and balance innovation with timely project delivery in a dynamic environment. Demonstrated success contributing to interdisciplinary, cross-functional projects. Desirable Experience in the pharmaceutical or biotechnology industry, particularly in translational medicine or [. .. ]
Job am 29.05.2026 bei Jobleads gefunden
Contract Negotiator
• Wien
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] training and experience. Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and then communicate these with study [. .. ]
Job am 29.05.2026 bei Jobleads gefunden
Clinical Pharmacist-Medicare
Position Summary The
Clinical Pharmacist performs retrospective
drug utilization reviews. They distribute clinical drug information and educate providers and staff regarding appropriate use of pharmaceutical treatment regimens. Responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Performing pharmacy review and making evidencebased recommendations regarding Medicare members. Identifying opportunities within the health plan for integration of quality measures in current case management or other clinical programs. Communicating [. .. ] practice guidelines to identify gaps in care and create/ communicate a recommendation plan to providers. Preferred Qualifications Board Certified Ambulatory Care Pharmacist, Board Certified Geriatric Pharmacist, or Board Certified Pharmacotherapy Specialist. Certified in MTM. Bilingual. Experience with Medicare STARS and Part D formulary benefit. Education BS in Pharmacy or Pharm D. Anticipated Weekly Hours 40 Time Type Full time Pay Range The typical pay range for this role is: 106, 200.00-225, 000.00 This pay range represents the base hourly [. .. ]
Job am 27.05.2026 bei Jobleads gefunden
Endoscopy Associate Clinical Specialist (Upstate NY-Buffalo/ Rochester)
Position Overview The Associate
Clinical Specialist independently provides customer support of Fujifilms ES equipment in the Endoscopy department and/or specified departments. This role manages all relevant equipment and uses its [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] own judgement and decision-making skills to provide troubleshooting and training for the proper handling of our equipment. This position provides on-site, handson client [. .. ] integration into a future database application. Attend local, regional, and national trade shows as requested. Adhere to all safety policies and procedures. Comply with all applicable U. S. Food and Drug Administration (U. S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. Qualifications High School Diploma or equivalent is required. Bachelors degree in business, marketing or related quantitative disciplines preferred. Minimum of 2 years of field sales or clinical experience desired. [. .. ]
1 von 3Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Specialist pro Jahr?
Als Clinical Drug Specialist verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 57 offene Stellenanzeigen für Clinical Drug Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Specialist Jobs?
Aktuell suchen 17 Unternehmen nach Bewerbern für Clinical Drug Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Drug Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Drug Specialist Stellenangebote:
- IQVIA (4 Jobs)
- Astra Zeneca (3 Jobs)
- Charles River (2 Jobs)
- Siegfried (2 Jobs)
- Syneos Health (1 Job)
In welchen Bundesländern werden die meisten Clinical Drug Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Specialist Jobs werden derzeit in Bayern (11 Jobs), Baden-Württemberg (7 Jobs) und Niedersachsen (6 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Specialist Jobs?
Clinical Drug Specialist Jobs gehören zum Berufsfeld Pharmazie.
