30 Jobs für Clinical Trial Specialist
Stellenangebote Clinical Trial Specialist Jobs
Job am 18.04.2026 bei StepStone gefunden
Edwards Lifesciences GmbH
• Bielefeld, Münster, Hannover
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
[. .. ] life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with [...]
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[...] cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Its our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. The goal will be to help make each site independent on procedures, product preparation and support. Field Clinical [. .. ] reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. Territory: Germany (Bielefeld, Münster, Hannover) How you will make an impact: Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical [. .. ] physicians and staff to reach expert proficiency in the THV procedure to deliver positive patient outcomes Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP Responsible for certification of the centers, physicians and other related staff, as well as EW personnel and as outlined within EW SOP Validate software and hardware updates in the field as applicable Regularly reviews clinical support activities, changes in the market and assigned accounts, as [. .. ]
Job am 02.04.2026 bei StepStone gefunden
Edwards Lifesciences GmbH
Field Clinical Specialist TMTT, Bonn/ Siegen
• Bonn, Siegen
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
[. .. ] more productive lives, our Field teams embrace Edwards Lifesciences values to build trusting, lasting relationships with medical professionals and industry partners. Your insight and dedication will help [...]
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[...] deepen and broaden clinical knowledge of our companys innovative technologies, while creating connections between providers and teams across our businesses to ensure patients receive the highest quality of care. Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit [. .. ] reviews clinical support activities and changes in the market assigned accounts Interact with KOL and proctors. Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP. Plan and implement growth strategies within focused accounts in partnership with the Sales and Sales Management. Learns the product (s) , physiology, anatomy, applications of the market and Edwards Lifesciences. Other incidental duties. What youll need (Required) : Bachelors Degree in related field (Biomedical Engineering [. .. ] full details regarding the entitlement and conditions for the benefits. Benefit policy and components may vary by location. . Edwards Lifesciences Gmb H sucht in Bonn, Siegen eine/n Field Clinical Specialist TMTT, Bonn/ Siegen (ID-Nummer: 13849179) 86138801 [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA LLC
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech
• AT- 9 Wien
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech page is loaded # # Clinical Associate Regulatory Submissions, Austria, IQVIA Biotechlocations: Vienna, Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1522611 [...]
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[...] Clinical Associate Submissions Regulatory Homebased Austria IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across [. .. ] accordance with applicable local and/or international regulations, standard operating procedures (SOPs) , project requirements and contractual/ budgetary guidelines. May also include maintenance activities. Essential Functions As Regulatory Start-Up Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. You will also ensure adherence to standard operating procedures (SOPs) , Work Instructions, quality of designated deliverables [. .. ] skills. Ability to work independently and to effectively prioritize tasks. Ability to manage multiple projects. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Understanding of regulated clinical trial environment and knowledge of drug development process. 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 treatments to help improve patient outcomes and population [. .. ]
Job am 28.03.2026 bei Mindmatch.ai gefunden
Fortrea
• AT- 9 Wien
A
clinical research organization is seeking a Clinical Start Up Contract Finance
Specialist in Vienna, Austria. This role focuses on overseeing clinical
trial submissions, managing country-level deliverables, and negotiating budgets. [...]
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[...] Ideal candidates will have a university degree, relevant experience in clinical research, and strong skills in budget negotiation. The position offers a hybrid work model and opportunities for professional development, contributing to impactful clinical research initiatives. J-18808-Ljbffr 85791597 [. .. ]
Job am 26.03.2026 bei Mindmatch.ai gefunden
Fortrea
FSP Start Up Contract Finance Specialist based in Vienna
• AT- 9 Wien
We are looking for a
Clinical Start Up Contract Finance
Specialist to support clinical
trial startup activities across Austria. This role is an excellent opportunity for professionals with experience in [...]
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[...] clinical startup operations, budget/ contract negotiations, and regulatory processes even if they have not previously worked in a Lead position. The successful candidate will receive development and support to grow into full leadership responsibilities while [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
PSI CRO
Site Identification Specialist
• AT- 9 Wien
[. .. ] committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Vienna, Austria This is the main responsibility of a site ID specialist. Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement. Project Responsibilities Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials. Define the main study objectives and the optimal site profile. Create initial list of potential sites. Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up [. .. ]
Job am 25.02.2026 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 [. .. ] or clinical research organization clinical 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 [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] on medical issuesproviding clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical [. .. ] safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with [. .. ]
Job gestern bei Jooble gefunden
Working Student (f/m/d) Clinical Marketing-Image Guided Surgery Robotics
• Landkreis Forchheim; Region Oberfranken- West, Bayern; Regierungsbezirk Oberfranken; Bayern
Werkstudenten
[. .. ] comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as W orking Student (w/m/d) to help us in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Clinical Marketing department (Image Guided Surgery and Robotics) . Choose the best place for your work Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60 of the respective working hours. Your tasks and responsibilities: [. .. ] portfolio in the fields of orthopaedics, traumatology, spinal surgery and vascular surgery You will help translate clinical findings into accessible language, explain study design, endpoints and key findings to non-specialist colleagues, and assist in the creation of training materials with a strong clinical focus You will contribute to the creation of professional Power Point presentations for internal and external audiences You will assist in the design and creation of internal training materials that help sales teams understand and communicate clinical [. .. ] (at least in your 4th semester) You are for a longer-term available (at least one year) You are confident using Power Point You have a sound understanding of clinical trial methodology (RCTs, endpoints, statistical significance) Some experience with video editing software would be an advantage Your attributes and skills: You have very good English skills; knowledge of German would be an advantage You are known for your independent, structured and results-oriented approach to work You impress with your ability [. .. ]
Job vor 3 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
Senior Site Activation
Specialist Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug [...]
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[...] 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. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] past 5 years, we have worked with 94 of all Novel FDA Approved Drugs, 95 of EMA Authorized Products and over 200 Studies across 73, 000 Sites and 675, 000+ Trial patients. No matter what your role is, youll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its [. .. ]
Job am 15.04.2026 bei Jooble gefunden
GSK
Clinical Operations Specialist Contracts (m/f/d)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] die Krankheitsmechanismen zu entwickeln und die medizinische Entdeckung zu transformieren. Wir revolutionieren unsere R D. Wir vereinen Wissenschaft, Technologie und Talente, um gemeinsam der Krankheit einen Schritt [...]
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[...] voraus zu sein. Clinical Operations Specialist (Contracts) (m/w/d) Als Clinical Operations Specialist führen und koordinieren Sie Aktivitäten im Zusammenhang mit Einreichungen gemäß ICH GCP, internationalen und lokalen Vorschriften sowie relevanten GSK-Standards. In dieser zentralen Rolle innerhalb unseres lokalen klinischen Studienteams sind Sie maßgeblich an der Planung, Durchführung und Überwachung klinischer Studien im Land [. .. ] Konsistenz, Kostenoptimierung und Risikominimierung sicherzustellen. Budgetaktualisierungen in Verträgen aufgrund von Protokolländerungen und Beratung bei der Anpassung des Studienbudgets sowie Identifikation von Kostenabweichungen und Möglichkeiten zur Kostenvermeidung. Sicherstellung der Vollständigkeit der Trial Master File (TMF) für alle Budget- und Vertragsaktivitäten und Unterstützung bei weiteren Aufgaben im Studienverlauf gemäß absolviertem Training. Qualifikationen Fähigkeiten Bachelor-Abschluss oder gleichwertiger Abschluss in einem wissenschaftlichen Bereich wie Biowissenschaften, Medizin, klinische Forschung, Pharmazie oder einem verwandten Fachgebiet. Relevante Erfahrung in der klinischen Forschung Fundierte Kenntnisse im Erstellen und [. .. ]
Job am 15.04.2026 bei Jooble gefunden
Clinical Operations Specialist with focus on finance
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Operations
Specialist with focus on finance Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs [...]
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[...] and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything [. .. ] as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits Maintains, updates, and inputs clinical tracking information into databases Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client R esponsibility in financial tracking and administration Manages shared mailbox, processes site [. .. ]
Job am 08.04.2026 bei Jooble gefunden
ICON
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Work-Life-Balance
CRA II/ Senior CRA-sponsor dedicated ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we [...]
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[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of in Nvative treatments and therapies What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelors degree in a scientific or healthcare-related [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Manager Clinical Trial Supply Management IMPM
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Drive
Clinical Supply Excellence Across Global Trials. Play a pivotal role in ensuring investigational medicines reach patients on time and in full compliance. Shape processes that accelerate innovative therapies [...]
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[...] worldwide. Manage and co-define initiatives of all Clinical Trial Supply Management IMPM activities in global Phase I-III clinical trials (R D Programs) . Your Contribution: Lead the coordination and execution of assigned clinical programs/ trials, acting as the primary interface between CTSM internal functions and trial teams. Serve as the point of contact for other departments (e. g. [. .. ] kit demand/patient units. Prepare IMP and IRT sections for investigator meetings, liaise with GCP Compliance for CRO trainings, and ensure adherence to ethical and regulatory standards. Manage and coach Specialist CTSM IMPM team members, fostering a culture of collaboration, innovation, and accountability. A Good Match: A relevant university degree in Supply Chain Management, Pharmacy, Chemistry, Biotechnology, Biochemistry, or a related discipline. At least 3 years of experience in Clinical Trial Supply Management or Project Management within the pharmaceutical or biotech [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Clinical Support Specialist-DACH Region
• Deutschland Deutschland, DE
[. .. ] magnetisch levitiertes LVAD-System für die langfristige mechanische Kreislaufunterstützung entwickelt. Als europäische Drehscheibe für ein global agierendes Technologieunternehmen vereint es klinische, regulatorische und ingenieurwissenschaftliche Expertise. Aktuell wird ein [...]
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[...] mehrzentrierter klinischer Trial durchgeführt, während parallel Aufbau, Schulung und Betreuung implantierender Kliniken in Europa vorangetrieben werden. Die Unternehmenskultur ist international, innovativ und geprägt von enger Zusammenarbeit mit Herzchirurgen, Perfusionisten und Intensivteams. Aufgabengebiet Vor-Ort-Betreuung während Implantationen sowie Unterstützung in der postoperativen Versorgung Beratung und Troubleshooting im OP und auf Intensivstationen zur optimalen [. .. ] ICU oder Perfusion Alternativ Erfahrung in einer klinischen oder feldnahen Rolle innerhalb der MCS oder kardiovaskulären Med Tech Industrie 1-5 Jahre relevante Berufserfahrung und Interesse an einer Weiterentwicklung zum Clinical Field Specialist Souveränität im Hochrisiko Umfeld (OP/ ICU) sowie technische Neugier und hohe Lösungsorientierung Fähigkeit, eigenständig im Feld zu arbeiten und sicher zu entscheiden, wann Eskalationen notwendig sind Hohe Reisebereitschaft und Flexibilität innerhalb Deutschlands, Österreichs und der Niederlande Professionelles Auftreten, Belastbarkeit und ausgezeichnete Kommunikationsfähigkeiten Sehr gute Deutschkenntnisse sowie sichere Englischkenntnisse Vergütungspaket Einstieg [. .. ]
Job gestern bei Jobleads gefunden
Contract Negotiator 2-FSP-German speaker
• Frankfurt, Hesse
[. .. ] 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 [. .. ] or clinical research organization clinical 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 [. .. ]
Job gestern bei Jobleads gefunden
Clinical Sample Specialist
• Köln, Nordrhein- Westfalen Koeln
Overview Lab Connect improves lives by partnering with pharmaceutical and biotech companies, and
clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are [...]
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[...] an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailormade, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service [. .. ] extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. Job Summary The Clinical Sample Specialist is responsible for sample management activities for samples arriving at Lab Connect Cleveland facility. The role will perform tasks in support of receiving specimens for storage, onsite processing, or shipments to partner laboratories or other facilities. The role will also communicate with other departments such as Client Services (CS) , Sample Tracking Solutions (STS) , and Clinical Trial Materials (CTM) to ensure the timely and accurate handling of samples. Essential Duties and Responsibilities Ensure tasks and data are completed with accuracy and attention to detail. Sample shipment receipt, inbound tracking documentation, and breakdown of kits received. Specimen transport to different areas within the facility. Order requisition registration and [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Global Change Management Lead Clinical Trials
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Proclinical Group in Basel-Stadt is seeking a dedicated
specialist to lead transformative change initiatives within
clinical trial oversight. The ideal candidate will have expertise in enterprise-scale change management, strong [...]
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[...] stakeholder engagement skills, and strategic thinking abilities. Responsibilities include overseeing change management plans, advising leaders, and measuring initiative effectiveness. This role requires a post-graduate degree, proficiency in structured change methodologies, and fluency in English. #J-[. .. ]
Job am 17.04.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Are you ready to lead transformative change that reshapes how
clinical trials are monitored and quality is delivered worldwide? Proclinical is recruiting for a dedicated
specialist to oversee [...]
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[...] the change management workstream and drive transformative change initiatives within clinical trial oversight. This role focuses on implementing central monitoring, adaptive monitoring, and innovative quality management approaches globally. You will play a pivotal role in ensuring the successful adoption of these strategies across functions and studies. Please note that to be considered for this role you must have the right to work [. .. ]
Job am 30.03.2026 bei Jobleads gefunden
Senior GMP QA Specialist (12-month FTC Maternity Cover) Senior GMP QA Specialist (12-month FTC. . .
• Hannover, Niedersachsen
[. .. ] The Company was founded with initial series A financing, led by Syncona Ltd who committed 83M with a further 1M contributed by UCL Technology Fund. THE ROLE [...]
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[...] The Senior QA Specialist (12-month FTC maternity cover) is responsible for the GMP oversight of clinical phase, gene-modified cell therapy product manufacturing and testing. This includes the execution and reporting of GSTT GMP PQS systems, the design, improvement, execution and reporting of Quell PQS systems, and oversight of outsourced GMP activities. This is an office-based role at Quells London Bridge office. MAIN RESPONSIBILITIES Day [. .. ] metrics driving right-first-time manufacturing and testing Draft, review and approve GMP documentation in accordance with Quells PQS requirements, GMP and other applicable regulatory standards, appropriate to the clinical trial phase and data criticality Provide support and advice for other functions within the business, for example, process and analytical research and development, internal and external manufacturing teams, patient supply operations and clinical operations. Design and deliver PQS related training as required Maintain oversight of PQS processes and provide guidance to [. .. ]
Job am 09.03.2026 bei Jobleads gefunden
Site Identification Specialist
• Wien
[. .. ] committed to delivering high-quality, timely services across a wide range of therapeutic areas. Job Description We are in search of an experienced professional dedicated to developing strategic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. Hybrid role in Vienna, Austria This is the main responsibility of a site ID specialist. Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement. Project Responsibilities Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials. Define the main study objectives and the optimal site profile. Create initial list of potential sites. Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
• Plan- les- Ouates, Genf
Do you want to work for an innovative
specialist spinal implant company and play a pivotal role in helping us in new market opportunities and optimizing pricing strategies? If [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] yes, join our financial team as Financial Planning Analysis Business Partner And become the key link between Finance and our Global Sales Marketing teams. Your main responsibilities will be: Commercial [. .. ] You are their go-to for financial clarity. Ensure alignment between commercial objectives and financial performance targets. Business Case: Build robust financial models for new product launches, market expansions, and clinical trial investments. Perform scenario and sensitivity analysis, evaluate ROI and payback, and provide structured recommendations to support capital allocation. Profitability Management: Analyse gross margins and net profitability by region, product line, and distributor. Identify leakage and suggest corrective actions. Recommend and follow corrective actions to improve contribution margins and overall financial [. .. ]
Job am 07.03.2026 bei Jobleads gefunden
Director Regulatory Affairs Oncology (m/f/d)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] for patients, their families, and society. Purpose of the function To serve as European Lead providing regulatory strategy support for assigned projects, products and nonproject work. Act [...]
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[...] as a regulatory specialist in the therapeutic area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of multidisciplinary global product teams, providing expertise on regulatory matters. Represent Regulatory Affairs in external interactions (e. g. authorities, affiliates, partners, CROs) , providing expertise for regulatory strategy to achieve regional and global company goals. Roles and Responsibilities Act as European regulatory lead supporting assigned projects in different stages of clinical development (early Phase 1-Phase 3) covering product development plans, clinical trial and marketing authorization applications (MAA) as well as product life cycle management. Develop and lead regulatory strategies for drugs and biologics, including orphan drug designation (ODD) , paediatric development plans (PIP) , clinical trial applications, submission dossiers for MAAs, and interactions with national European Health Authorities and EMA. Represent European [. .. ]
Job am 05.03.2026 bei Jobleads gefunden
Field Clinical Specialist Münster-Hannover
[. .. ] innovative, lifechanging solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Its our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. The goal will be to help make each site independent on procedures, product preparation and support. Field Clinical [. .. ] reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. Territory: Germany (Bielefeld, Münster, Hannover) How you will make an impact: Working independently in the areas of valve crimping, case management, precase planning, postcase management, 3 Mensio management, Therapy Awareness program management and clinical education programs [. .. ] physicians and staff to reach expert proficiency in the THV procedure to deliver positive patient outcomes Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP Responsible for certification of the centers, physicians and other related staff, as well as EW personnel and as outlined within EW SOP Validate software and hardware updates in the field as applicable Regularly reviews clinical support activities, changes in the market and assigned accounts, as [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
Contract Negotiator 2-FSP-German speaker
• 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 [. .. ] or clinical research organization clinical 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 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Specialist pro Jahr?
Als Clinical Trial Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 30 offene Stellenanzeigen für Clinical Trial Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Clinical Trial Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Specialist Stellenangebote:
- Edwards Lifesciences GmbH (2 Jobs)
- Fortrea (2 Jobs)
- IQVIA LLC (1 Job)
- PSI CRO (1 Job)
- IQVIA (1 Job)
- GSK (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Specialist Jobs werden derzeit in Bayern (6 Jobs), Nordrhein-Westfalen (4 Jobs) und Niedersachsen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Specialist Jobs?
Clinical Trial Specialist Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
