50 Jobs für Clinical Documentation Specialist
Stellenangebote Clinical Documentation Specialist Jobs
Job am 03.10.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Jobticket
[. .. ] Order Management Specialist (m/w/d) Frankfurt am Main, Hesse, Germany 3 weeks ago Frankfurt Rhine-Main Metropolitan Area 2 days ago Frankfurt am Main, Hesse, Germany 3 days ago [...]
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[...] Clinical Documentation Specialist (m/w/d) Beauty Consultant (m/w/d) Kosmetik/ Beauty Frankfurt am Main, Hesse, Germany 2 weeks ago Internship Fellow Consultant (f/m/d) Chemicals Life Sciences Junior Relationship Manager Global Corporate Banking Division Frankfurt Rhine-Main Metropolitan Area 2 days ago Frankfurt am Main, Hesse, Germany 3 weeks ago [. .. ]
Job vor 2 Tagen bei Jobware gefunden
Katharinenstift Heilbronn gGmbH
Pflegefachkraft (m/w/d) für den stationären Bereich
• Heilbronn
Teilzeit Abgeschlossene Ausbildung
Betriebliche Altersvorsorge 30+ Urlaubstage Tarifvertrag
[. .. ] Wochenenddienst Arbeit im multiprofessionellen Team Bewohnerorientierte Pflege Dokumentation im digitalen System Umgang mit Pflegehilfsmitteln Hygienevorschriften/ Infektionsschutz Pflegequalität sichern Basale Stimulation Palliativpflege Gerontopsychiatrie Intensivpflege-Erfahrung Schmerzmanagement Praxisanleitung Registered Nurse [...]
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[...] (RN) Nursing Specialist Inpatient Care Residential Care Long-term Care Elderly Care/ Geriatric Care Basic Nursing Care Clinical Nursing Treatment Care Care Planning Nursing Documentation Care Assessment Nursing Process Medication Management Wound Care/ Wound Management Preventive Care/ Prophylaxis Quality Management in Nursing Patient/ Resident Monitoring Empathy Communication Skills Teamwork Reliability Responsibility Stress Resilience Patience Problem-solving skills Time Management Compassion Shift Work Weekend Shifts Working in Interdisciplinary Teams Resident-centered Care Digital Documentation Systems Use [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
Clinical Site Technology
Specialist (Nuclear Medicine) PSI is a leading Contract Research Organization with more than 29 years in the industry offering a perfect balance between stability and innovation to [...]
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[...] both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Site [. .. ] other technologies Determine technical resources needed for project implementation, and communicate needs to department managers Organize technical training for project teams Provide support to the project teams to ensure proper documentation of study-specific assessments related to study technologies Support site initiation preparation and perform technical visits to assist the site team with technical aspects of the study Assist and advise the site monitor in the area of study technologies Provide relevant technology-related information to Business Development for proposals Prepare [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Medtronic
Senior Therapy Specialist (m/w/d)
• AT- 9 Wien
Homeoffice möglich
Join to apply for the Senior Therapy
Specialist (m/w/d) role at Medtronic At Medtronic you can begin a lifelong career of exploration and innovation, while helping champion healthcare access and [...]
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[...] equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Atrial fibrillation affects [. .. ] Senior AFFERA Mapping and Therapy Specialist to join our team to further drive the growth of the business. Reporting to the operating unit this role is critical in providing expert clinical and technical support and training to physicians and EP Lab Staff on the optimal use of the AFFERA Mapping and Ablation System. Bring your talents to a leader in medical technology and healthcare solutions. We support your growth with the training, mentorship, and guidance you need to own your future [. .. ] department, and marketing to ensure system efficiency, provide feedback, and contribute to new product development. Stay updated on product information, IFUs, scientific literature, and compliance with all company trainings and documentation requirements. Actively participate in congresses, symposia, and workshops regionally and internationally to represent Medtronic and share clinical best practices. Required Knowledge and Experience: Bachelors degree in electrical or medical engineering, or related scientific disciplines. A minimum of 3 years of clinical electrophysiology (EP) experience. At least 2 years of proven [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
• AT- 7 Kundl
A technology group specializing in
documentation solutions is seeking an expert to optimize documentation processes. The ideal candidate will have a strong background in medical device regulation, document management, and [...]
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[...] collaboration with cross-functional teams. Responsibilities include improving design control procedures and preparing clinical evidence documentation. The role offers a gross annual salary starting at EUR 69, 000, flexible working conditions, and opportunities for professional growth. J-18808-Ljbffr 71022548 [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Medtronic plc
Senior Therapy Specialist (m/w/d)
• AT- 9 Wien
Homeoffice möglich
Senior Therapy
Specialist (m/w/d) page is loaded # # Senior Therapy Specialist (m/w/d) remote type: Remotelocations: Vienna, Vienna, Austriatime type: Full timeposted on: Posted Todaytime left to apply: End Date: [...]
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[...] December 2, 2025 (4 days left to apply) job requisition id: R25987At Medtronic you can begin a life-long [. .. ] motivated Senior AFFERA Mapping and Therapy Specialist to join our team to further drive the growth of the business. Reporting the operating unit this role is critical in providing expert clinical and technical support and training to physicians and EP Lab Staff on the optimal use of the AFFERA Mapping and Ablation System. Bring your talents to a leader in medical technology and healthcare solutions. We support your growth with the training, mentorship, and guidance you need to own your future [. .. ] ensure system efficiency, provide feedback, and contribute to new product development. Regulatory and Scientific Compliance Stay updated on product information, IFUs, scientific literature, and compliance with all company trainings and documentation requirements. Professional Representation Actively participate in congresses, symposia, and workshops regionally and internationally to represent Medtronic and share clinical best practices. Required Knowledge and Experience: Bachelors degree in electrical or medical engineering, or related scientific disciplines. A minimum of 3 years of clinical electrophysiology (EP) experience. At least 2 years [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
• AT- 7 Kundl
[. .. ] for prestigious clients, aiming to discover and nurture human potential by creating tailored connections between companies and talents. Bring your expertise to our projects and actively shape [...]
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[...] the future. Responsibilities Documentation Excellence: Drive lean, compliant, and scientifically sound documentation processes by optimizing and digitalizing Design History Files (DHF) for efficient knowledge management. Cross-Functional Collaboration: Partner with R D, Quality, and Regulatory teams to streamline technical development processes for faster and more effective product development. Data-Driven Process Improvement: Leverage data [. .. ] functions; coordinate complex, cross-functional changes. Technical Documentation Authoring: Co-author new platform and pioneer project documents with Subject Matter Experts (SMEs) to establish clear, compliant, and innovative technical content. Clinical Evidence Documentation: Prepare and maintain Clinical Evidence Assessment documents that support regulatory and clinical validation requirements. Design Control Optimization: Support the creation and continuous improvement of Design Control procedures, ensuring alignment with global quality and compliance standards. Qualifications Education Experience: Bachelors, Masters, or Ph D in Engineering or Natural Sciences with [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
UEG- United European Gastroenterology
Project Manager-Scientific Programme Implementation (m/f/d) (m/w/d)
• AT- 9 Wien
Homeoffice möglich
[. .. ] Full-time (37, 5 hours/ week) Location : Wickenburggasse 1, 1080 Vienna About UEG UEG, or United European Gastroenterology, is a professional nonprofit organisation combining all the leading [...]
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[...] European medical specialist and national societies focusing on digestive health. The mission of UEG is to improve the prevention and care of digestive diseases in Europe through providing education, supporting research and improving clinical standards. UEGs headquarters is in Vienna, Austria where we coordinate all association, education and congressrelated matters. All other important information regarding our organisation can be found on our website at The open position We are seeking a highly organized and proactive project manager to support the planning and implementation of our scientific and educational programmes. In this role, you will coordinate project timelines, manage administrative workflows, liaise with academic committees and scientific experts, prepare documentation and meeting materials, and ensure smooth delivery of all programmerelated activities for the annual congress UEG Week. If you are motivated, structured, and enjoy supporting scientific work through excellent administration, we look forward to your application. Responsibilities Provide operational and administrative support in planning, coordinating, and delivering the scientific and [. .. ]
Job am 24.07.2025 bei Mindmatch.ai gefunden
Canonical
• AT- 9 Wien
[. .. ] our teams, and in doing so we aim to level up our insights on scalability, performance, resilience and Dev Ops practices. Key areas of interest for us [...]
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[...] are: API design, documentation, and governance Database performance design considerations and skills Multi-region service delivery for resilience and performance Fuzzing and other proactive security analysis techniques Tracing and profiling for distributed systems insights Next-generation Dev Ops practices Location : we have microservices teams with open roles in every time zone. What your [. .. ] Junior Software Engineer-Cross-platform C++-Multipass Outside Sales Engineer-Austria/ Switzerland (m/w/d) Wiener Neudorf, Lower Austria, Austria 3 weeks ago Software Engineer (Python/ Linux/ Packaging) Junior Mapping Clinical Specialist (m/f/d) Python Backend Senior Software Engineer-Remote 4 days a week (Europe) Software Engineering Manager-Sustaining Engineering Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. J-18808-Ljbffr 56107340 [. .. ]
Job gestern bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
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[...] service-capabilities, resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, [. .. ] as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions : Offer expert medical insight into regulatory submissions and 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-[. .. ]
Job am 27.06.2025 bei Jobleads gefunden
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 [...]
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[...] 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, [. .. ] Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Data Analytics Specialist 70/ hr
Clinical Data Analytics
Specialist 70/ hr Join to apply for the Clinical Data Analytics Specialist 70/ hr role at Mercor Overview Mercor connects elite creative and technical talent [...]
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[...] with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam DAngelo, Larry Summers, and Jack Dorsey. Position details Position: Technical Documentation Specialist Type: Part-time Contract Compensation: 5070/ hour Location: Remote Commitment: 1020 hours/ week Role Responsibilities Review clinical reports, technical reviews, and grant proposals for clarity and rigor. Evaluate experimental methodologies and interpret their validity in supporting outcome claims. Draft concise, technical summaries of research methods and results. Provide structured [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Join to apply for the Medical Device Software
Specialist role at BSI Job Title Technical Specialist, Scheme Manager,
Clinical Evaluation Specialist-Sa MD Reports to Technical Team Manager Location [...]
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[...] Home Based Global Purpose of the position To build, manage, develop, control and manage a portfolio of Medical Device CE marking schemes. To deliver technical documentation assessments in support of the CE marking schemes. To provide Medical Device expertise leadership and mentoring in areas of competence to Healthcare personnel. Key Responsibilities Accountabilities Plan and deliver Technical File Assessments, Design Examinations and Unannounced Audits to support EC Certification. Manage client projects, acting as their primary contact and [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Lead (Class II/ III)
Führungs-/ Leitungspositionen
A leading life sciences recruiter is seeking a Medical Device
Clinical Safety
Specialist in Switzerland to oversee clinical safety activities for Class II and III medical devices. The [...]
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[...] ideal candidate will have a degree in a scientific field and experience in clinical safety. Key responsibilities include managing the vigilance process, contributing to study documentation, and conducting benefit-risk assessments. Excellent communication and leadership skills are essential for this role. #J-18808-Ljbffr 70308765 [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Ready to lead
clinical safety and help bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference Proclinical is seeking [...]
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[...] a Medical Device Clinical Safety Specialist to provide expertise and support across all safety-related aspects of Class II and/or III medical devices, with a focus on clinical investigations. This role involves collaborating within cross-functional teams and independently leading the development of safety deliverables. Please note that to be considered for this role you [. .. ] compliance with global regulations and internal standards. Manage the vigilance process, including adverse event intake, processing, assessment, and reporting to regulatory authorities. Review and contribute to core medical device study documentation, such as Clinical Investigation Plans (CIP) , Protocols, and Investigator Brochures (IB) . Develop and maintain Reference Safety Information (RSI) for clinical investigations, ensuring accuracy and timely updates. Conduct or contribute to benefit-risk assessments for medical devices, interpreting clinical safety data to inform decisions. Apply risk management principles in [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Senior QA Specialist-Project Manager 80-100 (f/m/d)
• Visp, Wallis
[. .. ] want to be part of. For our Quality Assurance team in Bioconjugates, Visp we are currently looking for a dedicated person who would like to work as [...]
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[...] a Senior QA Specialist and a Project Manager (f/m/d) in a fast-growing and innovative environment. In this role you will support clinical phase manufacturing and will interact with internal and external stakeholders to represent Quality. Key Responsibilities As a member of the QA team (Bioconjugates) , you will be responsible for ensuring production of APIs is in accordance with Good Manufacturing Practice (GMP) . Support the contract manufacturing and advise members of development, production, and analytical departments on all aspects of GMP. Responsible for checking manufacturing documentation for conformity, processing change controls, and reviewing and approving deviations and OOS results. In addition, you will be the quality contact for our clients, and will present during their GMP audits. Key Requirements University degree in Life Sciences (Microbiology/ Biotechnology/ Chemistry etc) . First experience in the GMP environment required, [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
At Gradientech, innovation meets purpose. Were looking for a passionate Field Application
Specialist DACH region to be the bridge between their revolutionary Quick MIC system and the
clinical [...]
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[...] laboratories that rely on its precise performance of rapid antibiotic susceptibility testing (r AST) every day. In this role, youll primarily support customers within Germany and the DACH-region, while also engaging with laboratories and distributors in nearby markets. If youre driven by science, technology, and making healthcare faster, smarter, and [. .. ] conferences, and trade shows, presenting the Quick MIC technology and the systems capabilities. Give input and collaborate with the marketing team to create and maintain highquality marketing material and clear technical documentation to ensure effective knowledge transfer for various scientific presentations and competitor positioning. About you Degree in microbiology, clinical chemistry, biomedical science or a related field a Ph D degree is preferred. At least 25 years of working experience from clinical diagnostic labs or industry field application support roles. Excellent communication and [. .. ]
Job am 10.11.2025 bei Jobleads gefunden
Contract Specialist-hybrid in Munich
• München, Bayern
Principal Sourcing
Specialist Syneos Health Contract Specialist hybrid in Munich Syneos Health is a leading fully integrated biopharmaceutical solutions organization that accelerates customer success. It translates unique
clinical, [...]
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[...] medical affairs and commercial insights into outcomes to address modern market realities. The companys clinical development model places the customer and the patient at the centre of everything it does, continually simplifying work to make Syneos Health easier to work with and to work for. Whether you join us in [. .. ] members with the active project management of ongoing contract issues; performs followup on all outstanding contract issues. Supports generating amended contract and/or budget documents as necessary, preparing contract management documentation for projects, and streamlining the contract/ proposal or internal processes; and initiates and introduces creative ideas and solutions. Works within the forecasted country/ site contracting timelines, ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time. Collaborates with internal and external legal, [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
• Lähden, Niedersachsen
Clinical Education Nurse South Inizio Engage Competitive Salary + Excellent Benefits Field-based Covering South West, London South East About the Role Are you an experienced nurse educator who enjoys [...]
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[...] combining teaching with handson clinical practice? Were looking for a motivated Clinical Education Nurse to join our dynamic fieldbased team across [. .. ] training programmes (facetoface and virtual) Assess, mentor and maintain nurses competencies in line with clinical standards and best practice Support onboarding, upskilling and ongoing professional development of nursing staff Provide specialist communitybased care to patients when required Act as a clinical role model, promoting excellence and evidencebased practice Conduct audits and reviews to ensure training quality, compliance and clinical governance Maintain accurate documentation in line with SOPs, SEOPs and the NMC Code of Practice Collaborate with regional teams to continuously improve training delivery and patient outcomes About You Were seeking a credible and enthusiastic clinician with a strong background in education and a passion for supporting others. Current NMC registration (RN, RGN or [. .. ]
Job am 05.11.2025 bei Jobleads gefunden
Professorship (W2) in Clinical-Experimental Reproductive Medicine (six years/ tenure track)
• München, Bayern
[. .. ] broad spectrum that covers all areas of knowledge within its 18 Faculties, ranging from the humanities, law, economics and social sciences, to medicine and the natural sciences. [...]
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[...] The Centre for Clinical Veterinary Medicine, Faculty of Veterinary Medicine, invites applications for a Professorship (W2) (six years/ tenure track) in Clinical-Experimental Reproductive Medicine commencing as soon as possible. The successful applicant will be responsible for all aspects within the field of animal reproduction. The successful applicants activities are expected to extend into [. .. ] specific qualification. Candidates are expected to demonstrate their potential for an outstanding academic career with an excellent record in research, teaching and, if applicable, clinical service. National recognition as veterinary specialist or international board certification is expected. The initial appointment will be for six years. After a minimum of three years, it can be converted into a permanent position pending a positive evaluation of the candidates performance in research and teaching as well as his or her personal aptitude and if [. .. ] to enhance the diversity of its faculty members. Furthermore, disabled candidates with essentially equal qualifications will be given preference. Please submit your application in English comprising of a curriculum vitae, documentation of academic degrees and certificates as well as a list of publications, teaching activities, third-party funding and a research concept to the Dean of the Faculty of Veterinary Medicine, Ludwig-Maximilians-Universität München, Veterinärstr. 13, 80539 Munich, Germany, via electronic submission (, one single pdf file with max. 10 [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
Quality Regulatory Dossier Compliance Specialist (m/f/d)
• München, Bayern
[. .. ] Freiburg) . The Courroux site is multifunctional, specialized in manufacturing parenteral products, it employs over 100 employees, and is recognized as a European leader in the manufacture [...]
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[...] and supply of clinical trial medications. Adragos Jura is seeking a Regulatory Dossier Compliance Specialist to support regulatory compliance and contribute to the submission and maintenance of national and international authorizations for our customers. The role will operate under the guidance of a Quality Compliance Systems Team Leader and will involve collaboration with crossfunctional teams both internally and with customers to ensure timely and accurate [. .. ] internal teams and our customers, support the preparation, submission, and maintenance of product registrations across global markets (EU, Switzerland, FDA, and Rest of World) . Independently and critically review regulatory documentation for marketing authorization applications (MAAs) , to support variations, renewals, and other regulatory activities. Coordinate with internal departments, local partners, Marketing Authorization Holders (MAHs) , ensure high-quality submissions. Compare product manufacturing and testing particulars against regulatory filings to ensure comfortable compliance. Evaluate impact of Change Controls and CAPAs on [. .. ]
Job am 26.10.2025 bei Jobleads gefunden
Field Service Engineer
• Kaarst, Nordrhein- Westfalen
Join to apply for the Field Customer Support
Specialist role at Charles River Laboratories 4 days ago Be among the first 25 applicants Join to apply for the Field [...]
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[...] Customer Support Specialist role at Charles River Laboratories Get AI-powered advice on this job and more exclusive features. For 75 years, Charles River employees have worked together to assist [. .. ] installation, qualification, routine preventive maintenance and product performance analysis Provide technical support and problem resolution to customers via phone, email or on-site Complete all required field service activities and documentation as assigned based on specific product, customer and/or standard operating procedures Assist sales representatives with product demonstrations, new customer training and product validations Responsible for completing all service and compliance documentation in accordance with company policies-c GMP and FDA Responsible for resolving service issues with customer test lab equipment [. .. ] Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20, 000 employees within 110 facilities in over 20 [. .. ]
Job am 26.10.2025 bei Jobleads gefunden
Special Operations Physical Therapist (Baumholder, Germany)
• Stuttgart, Baden- Württemberg
[. .. ] for HP staff as directed by governing credentialing bodies and local medical oversight processes. Assist in developing and updating criteriabased job descriptions and performance standards. Assist in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] developing and maintaining clinical practice guidelines across HP Training Centers and associated facilities. Assist with short and longterm fiscal planning and submit input to the HP Program Manager/ Coordinator. Attend and participate in meetings with other POTFF staff and medical providers as required. Ensure safe and effective operation of patientcare equipment and contribute to [. .. ] or SOF Operator settings. Fluent oral and written communication skills in English. Current Basic Cardiac Life Support (BCLS) certification by the American Heart Association; must provide proof of training and documentation. Desired Education, Experience, Skills or Training Doctoral degree in Physical Therapy. Prior military and/or SOF experience. Additional credentials such as Certified Strength and Conditioning Specialist (CSCS) through NSCA. Standard Company Requirements Compliance with Safety, Health and Environmental plan, policies and procedures. Compliance with the Quality Assurance plan, policies and procedures. Maintain regular and acceptable attendance. Complete all required training. Perform other assignments and duties as required. KBR Benefits KBR offers a selection of competitive lifestyle [. .. ]
Job am 23.10.2025 bei Jobleads gefunden
QA Manager Medical Device Development (m/f/d) , R D Quality
• Frankfurt, Hesse
[. .. ] like to become part of our success story? Then join Merz Aesthetics You lead R D project teams through Design Control requirements, ensuring compliance across development phases, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supporting preclinical and clinical planning, contributing to regulatory submissions, and facilitating smooth transfer to manufacturing. You manage risk and usability processes, guiding activities, documentation, and cross-functional input throughout all stages of the product development lifecycle, including maintaining the risk management plan, risk file, and usability strategies. You support audits and inspections, preparing for and participating in inter nal and external audits, and addressing findings in collaboration with relevant stakeholders. You ensure R D [. .. ] Ongoing training Your personal and professional development is the key to success for us. To foster this, we conduct regular development discussions and facilitate a wide range of management and specialist training courses, soft skills courses, e-learning courses, language courses and coaching sessions. #J-18808-Ljbffr 66992654 [. .. ]
Job am 19.10.2025 bei Jobleads gefunden
Clinical Specialist, South Germany
• Frankfurt, Hesse
[. .. ] of non-invasive patient monitoring at the customers site Development and implementation of individual overall solutions for the customer together with the sales staff and subsequent continued support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Training of clinical and nursing staff in the companys own training center or in hospitals Product presentation in workshops, at trade fairs and congresses Documentation and forwarding of customer feedback in the CRM system Collaboration with national and international teams such as Customer Service, Marketing and Technical Service Traveling in the assigned region at least 60 of the working time Requirements: High school diploma with subsequent medical training, e. g. as a cardio technician, nurse [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Documentation Specialist pro Jahr?
Als Clinical Documentation Specialist verdient man zwischen EUR 50.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Documentation Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 50 offene Stellenanzeigen für Clinical Documentation Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Documentation Specialist Jobs?
Aktuell suchen 15 Unternehmen nach Bewerbern für Clinical Documentation Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Documentation Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Documentation Specialist Stellenangebote:
- Planet Pharma (11 Jobs)
- Katharinenstift Heilbronn gGmbH (2 Jobs)
- Teccon GmbH Co. KG (2 Jobs)
- S3 Science Recruitment (2 Jobs)
- PSI CRO (1 Job)
- Medtronic (1 Job)
In welchen Bundesländern werden die meisten Clinical Documentation Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Documentation Specialist Jobs werden derzeit in Nordrhein-Westfalen (8 Jobs), Bayern (5 Jobs) und Baden-Württemberg (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Documentation Specialist Jobs?
Clinical Documentation Specialist Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
