107 Jobs für Clinical Documentation Specialist
Stellenangebote Clinical Documentation Specialist Jobs
Job am 17.01.2026 bei StepStone gefunden
Medicaroid Europe GmbH
• Düsseldorf
Homeoffice möglich
[. .. ] to join our Medicaroid Europe Gmb H headquarter in Düsseldorf, Germany, founded in 2020, to help drive the adoption and advancement of robotic-assisted surgery across Europe. As [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Robotic Implementation Specialist at Medicaroid Europe Gmb H, you will play a pivotal role in driving the implementation and adoption of the hinotori robotic surgery system in the hospital. you will engage and collaborate with internal external stakeholders to deliver comprehensive technical support, enabling confident and efficient use of the hinotori in the OR. [. .. ] Europe Gmb H and the customer site. Model: On field-Hybrid Travel: minimum 6 Experience in the OR setting or understanding of the OR setting and dynamics Min. 2 years of clinical experience or commercial experience in similar role Personal hands-on technical aptitudes, with willingness to learn complex and advanced medical equipment. Excellent interpersonal communication skills Ability to work under pressure and strict deadlines Ability to work alone and in multidisciplinary teams to achieve the KPIs of the company Ability to [. .. ] of the role High organizational and time management skills, prioritizing appropriately the task and the support provided Ability to escalate situations appropriately in a timely fashion Proficiency in information gathering, documentation and report writing Ability to lead and work on projects B2 verbal and written English required C2 verbal and written German Required Flexibility to travel also during unsocial hours On field support for a minimum of 60 of the time Personal motivation and striving for improvement and development The position [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
Skills Trainer m/w/d
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787736 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787735 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
eppdata GmbH
Information Security Manager (m/f/d)
• Hamburg
Work-Life-Balance
What do you do at Eppdata Improve and maintain an information security management system and
documentation Information security risk management Network security appliance configuration and management (Firewall, IDS/ IPS, antivirus) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Identify security vulnerabilities and gaps and support and follow-up on remediation implementation Support and facilitation of external information security audits Support data protection management tasks Support preparation of ISO 27001 certification process What you bring along A completed apprenticeship as an IT specialist, a degree in computer science or comparable experience At least 3 years of related professional experience in an IT discipline Experience with information security and data privacy management (theoretical and practical, please provide existing certifications) Good understanding of networking Experience with Linux and Docker You communicate proactively and enjoy teamwork [. .. ] company bicycles, and more. Were committed to meeting individual needs and continuously expanding our benefits. About us Eppdata Gmb H is a growing service company offering information technology services for supporting clinical studies in the field of Neuroradiology with more than twenty internal employees. We are simplifying imaging data collection and use advanced data analytics and AI, accelerating patient access to new therapies and supporting the clinical study lifecycle. We welcome individuals of all genders, nationalities, and backgrounds to join our team. [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for training [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787737 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
Recruitment Training Manager:in
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787732 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
• Homeoffice
To support safe, consistent, high-quality adoption across
clinical and commercial environments, we are recruiting a Surgical Training Manager. You will be the go-to expert for surgical technique, responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the highest surgical and compliance standards. Location: United Kingdom or Germany (Remote) [. .. ] and ensure consistent training across clinical sites. Ensure compliance with GCP, SOPs, regulatory requirements, and reporting obligations (AEs, complaints) . Support wet labs and represent Ciliatech at congresses. Clinical Application Specialist, surgical nurse, clinical support) . Fluent in written and spoken English. Full compliance mindset (GCP, SOPs, documentation) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, French) . 77787733 [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Ciliatech
Surgical Training Manager-Europe
• Homeoffice
Ciliatech is expanding its European footprint with the launch of Intercil, a next-generation uveal spacer for glaucoma surgery. To support safe, consistent, high-quality adoption across
clinical and commercial environments, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] we are recruiting a Surgical Training Manager. This role is central to elevating surgical expertise internally and externally. You will be the go-to expert for surgical technique, responsible for training field teams, supporting surgeons during live cases, and ensuring that all clinical sites operate with the [. .. ] congresses. Maintain awareness of industry developments and share insights with senior management PROFILE Required Skills Experience Minimum 5 years of experience in ophthalmic operating rooms (e. g. , Clinical Application Specialist, surgical nurse, clinical support) . Prior experience in a training, coaching, or educational function. Fluent in written and spoken English. Strong communication skills and high emotional intelligence. Ability to coach, influence, and lead without formal authority. Strong organization skills with high attention to detail. Full compliance mindset (GCP, SOPs, documentation) . Ability to adapt to fast-changing environments and operate autonomously. Preferred Skills Experience Experience in Glaucoma or MIGS (Minimally Invasive Glaucoma Surgery) . Experience supporting clinical trials (training, monitoring, SIV support) . Experience in a medical device company. Ability to deliver training in another European language (Italian, Spanish, German, [. .. ]
Job am 20.01.2026 bei Jooble gefunden
KBR
• Stuttgart
[. .. ] following services in support of POTFFs HP program for SOF personnel, with the priority on SOF Operators and Direct Combat Support personnel: Provide neuro-musculoskeletal injury care, utilizing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] approved supplemental clinical privileges including the ordering of images, laboratory tests, pharmaceuticals, dry needling, acupuncture, joint injections and aspirations, and referrals to specialty providers. If directed by HP Program Manager and/or Coordinator, directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer (ATC) within their scope of practice. Participate in [. .. ] English. Must maintain current certification in Basic Cardiac L ife Support ( BCLS ) by the American Heart Association; m ust provide front and back proof of all training/ certs/ documentation. Desired Education, Experience, Skills or Training: Doctoral degree in Physical Therapy. Prior military and/or SOF experience. Additional credentials such as a Certified Strength and Conditioning Specialist (CSCS) through the National Strength and Conditioning Association ( NSCA ) . Standard Company Requirements: Must comply with Safety, Health and Environmental plan, policies and procedures. Must comply with the Quality Assurance plan, policies and procedures. Must maintain regular and acceptable attendance. Responsible for completing all required training. Perform other [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Hire Resolve. com
Mid-Senior Healthcare Professional
• Düsseldorf
[. .. ] healthcare organisations in hiring experienced healthcare professionals for a portfolio of midsenior level opportunities across hospital, outpatient, rehabilitation, and community care settings. This is a multi-role opportunity [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] covering several clinical functions, including senior nursing practice, allied health delivery, specialist patient management, and clinical/ team leadership. These roles offer clear progression toward senior clinician, team lead, and service leadership positions within regulated healthcare environments. Key Responsibilities Deliver safe, evidence-based, patient-centred care aligned with professional standards, clinical guidelines, and local protocols Conduct patient assessments, develop care plans, deliver interventions, [. .. ] service delivery within wards, clinics, therapy services, or community settings (role dependent) Collaborate within multidisciplinary teams to support care coordination, escalation, discharge planning, and continuity of care Maintain accurate clinical documentation and handovers using approved documentation standards and clinical systems Uphold infection prevention and control (IPC) , medication safety (where applicable) , and clinical risk management practices Participate in quality assurance and continuous improvement activities, including audits, incident reporting, and corrective actions Ensure compliance with applicable German healthcare quality and safety [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
• Berlin
Clinical Research Associate (CRA) Location: Germany (Remote ) Job Description: We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] monitoring and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, [. .. ] visits, follow-up, site contact, and report writing. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Attend study meetings and collaborate with cross-functional teams and study sites throughout all study phases. Ensure monitoring of informed consents and site study files, including documentation for patients experiencing serious adverse events (SAEs) . Report non-compliance of investigators with their Clinical Study Agreements (CSAs) to the [. .. ] in Poland since 1996 and later expanded to the Czech Republic and Hungary. Across the CEE region, we employ around 150 professionals who deliver a full range of services from specialist and executive recruitment, employee outsourcing and HR consulting, to employer branding and market research. Our division-based structure combines deep industry expertise with functional specialisation, enabling us to provide tailored solutions for companies in every sector. We act as a trusted partner for both employers and candidates, sharing our knowledge [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
Klinischer Monitor/ Clinical Research Associate
• Berlin
Clinical Research Associate (CRA) Location: Germany (Remote ) We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Report non-compliance of investigators with their Clinical Study Agreements (CSAs) to the Client. Support audit preparation and responses. Perform additional services or projects only upon written approval from the Client. Proven experience as a Clinical Research Associate (CRA) or equivalent role. Strong organizational, communication, and report-writing skills. Fluency in English; additional language skills (e. g. german) advantageous. Across the CEE region, we employ around 150 professionals who deliver a full range of services from specialist and executive recruitment, employee outsourcing and HR consulting, to employer branding and market research. Follow us on Linked In: 75125156 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
• Berlin
Clinical Research Associate (CRA) Location: Germany (Remote ) We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Report non-compliance of investigators with their Clinical Study Agreements (CSAs) to the Client. Support audit preparation and responses. Perform additional services or projects only upon written approval from the Client. Proven experience as a Clinical Research Associate (CRA) or equivalent role. Strong organizational, communication, and report-writing skills. Fluency in English; additional language skills (e. g. german) advantageous. Across the CEE region, we employ around 150 professionals who deliver a full range of services from specialist and executive recruitment, employee outsourcing and HR consulting, to employer branding and market research. Follow us on Linked In: 75125153 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
CRA II-Sponsor dedicated
• Frankfurt am Main
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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, [. .. ] 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 field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth k Nwledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability [. .. ]
Job vor 6 Tagen bei Neuvoo.com gefunden
UNIVERSITÄTSMEDIZIN der Johannes Gutenberg- Universität Mainz
• Rhineland- Palatinate Mainz
Jobticket
HIS Application Manager (f/m/d-IT Division,
Clinical Systems Department The IT division is looking for the Clinical Systems department at the earliest possible date HIS application administrator (f/m/d) The University [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Center of Johannes Gutenberg University Mainz is the only supramaximal care medical institution in Rhineland-Palatinate and an internationally recognized scientific location. Our more [. .. ] well as active participation in the introduction of a successor system Advising and supporting employees from the clinics in matters relating to patient administration and billing as well as clinical documentation Conducting training courses and workshops for users on how best to use the clinical systems Analysis, documentation and participation in the optimization of clinical IT processes and interfaces Your profile Successfully completed studies in (medical) computer science, completion of IT specialist training or a comparable qualification (e. g. medical/ nursing training with a high affinity for IT) Ideally experience in the support, administration or application of clinical information and application systems, preferably SAP IS-H/ i. s. h. med Very good understanding of clinical and administrative patient care processes desirable Team [. .. ]
Neu Job vor 5 Std. bei Jooble gefunden
Abb Vie
Project Manager Clinical Supplies Systems (all genders) (full-time, limited for 24 months)
• Ludwigshafen am Rhein
Work-Life-Balance
[. .. ] through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place Moving mountains together [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Project Manager Clinical Supplies Systems (all genders) As a Project Manager Clinical Supplies Systems you work on automation, digitalization and optimization requests to increase efficiency within CSM. You are responsible for day to day systems activities, like training and Master Data Management. You resolve system questions and interface issues directly communicating with users [. .. ] and collection of statistics and KPIS, as well as implementation of ad hoc views, dashboards, unvalidated reports. Development of IT solutions for new processes and process optimizations with the respective specialist area, from idea to testing to implementation with the support of supervisors. Processing primarily local inquiries about the functionality of CSM IT systems of various complexity and urgency. Involving global IT support and external system providers. Communication with global users of CSM IT systems, to discuss specific inquiries and problem [. .. ] master data management into the CSM IT system, as per requests and information from various source systems. Influence on all relevant system functionalities must be considered. Support system lifecycle activities, documentation, UAT approvals, system access approvals and coordination of upgrade and system change activities with respective business and IT partners. Definition of new local processes within CSM from the perspective of system functionalities, as well as when writing user requirement specifications. Preparation and update of global SOPs, work instructions and training [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Universitätsklinikum Hamburg- Eppendorf
• Hamburg
[. .. ] participation in the design and introduction of innovative degree programmes at the UKE, as well as in the stronger integration of digital teaching formats Close cooperation with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] other preclinical and clinical subjects in the area of teaching Teaching commitments Teaching load according to the Teaching Obligation Regulation for Hamburg Institutions of Higher Education LVVO in its currently valid version. A reduction in the teaching load is gov-erned according to Sections 15 et seq. LVVO. Your Profile In accordance with Section [. .. ] of 18 July 2001, as amended, including proof of a postdoctoral lecturing qualification or an equivalent scientific qualification in pharmacology Completed degree in medicine or a biomedical science and doctorate Specialist qualification in Pharmacology and Toxicology or recognition as a pharmacologist by the German Society of Pharmacology (DGP) Outstanding publications and high international visibility in the field of experimental pharmacology Recognised research achievements, in particular through the successful acquisition of public third-party funding (e. g. DFG, BMBF, EU) Experience in [. .. ] teaching formats is desirable Immunity status Please note that employment is contingent upon proof of immunization or immunity against the measles virus, in accordance with applicable legal and medical requirements. Documentation (e. g. , vaccination certificate) must be provided before employment begins. Our Offer An innovative and family-friendly working environment in the heart of Hamburg (collaboration with childcare providers, free childcare during school/ kindergarten holidays) Opportunity to participate in extensive training and continuing education programs at our UKE Academy for [. .. ]
Job vor 6 Tagen bei JobMESH gefunden
UNIVERSITÄTSMEDIZIN der Johannes Gutenberg- Universität Mainz
HIS Application Manager (f/m/d) - IT Division, Clinical Systems Department
• Rheinland- Pfalz Mainz
Jobticket
HIS Application Manager (f/m/d-IT Division,
Clinical Systems Department The IT division is looking for the Clinical Systems department at the earliest possible date HIS application administrator (f/m/d) The University [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Medical Center of Johannes Gutenberg University Mainz is the only supramaximal care medical institution in Rhineland-Palatinate and an internationally recognized scientific location. Our more [. .. ] well as active participation in the introduction of a successor system Advising and supporting employees from the clinics in matters relating to patient administration and billing as well as clinical documentation Conducting training courses and workshops for users on how best to use the clinical systems Analysis, documentation and participation in the optimization of clinical IT processes and interfaces Your profile Successfully completed studies in (medical) computer science, completion of IT specialist training or a comparable qualification (e. g. medical/ nursing training with a high affinity for IT) Ideally experience in the support, administration or application of clinical information and application systems, preferably SAP IS-H/ i. s. h. med Very good understanding of clinical and administrative patient care processes desirable Team [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Stryker
• Augsburg
Clinical Specialist, Joint Replacement Insert Location Overview As a Clinical Specialist at Stryker, you will help improve orthopedic surgeries around the world and play a direct role in our mission [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of making healthcare better. In this role, you will build deep clinical and technical expertise across both robotic (Mako Smart Robotics) and [. .. ] programs, and customer training events. Build and maintain strong, trust-based relationships with surgeons, OR staff, and cross-functional partners. Manage administrative tasks related to accounts, system updates, and case documentation. Collaborate with sales partners to ensure seamless execution and a unified customer experience. Complete required trainings, competencies, and certifications. Provide on-call coverage during evenings, weekends, and holidays. What You Need Minimum Required: Bachelors degree OR Associate degree with 4 years of professional and/or related experience OR High school [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Hire Resolve. com
Mid-Senior Healthcare Professional
• Frankfurt am Main
[. .. ] healthcare organisations in hiring experienced healthcare professionals for a portfolio of midsenior level opportunities across hospital, outpatient, rehabilitation, and community care settings. This is a multi-role opportunity [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] covering several clinical functions, including senior nursing practice, allied health delivery, specialist patient management, and clinical/ team leadership. These roles offer clear progression toward senior clinician, team lead, and service leadership positions within regulated healthcare environments. Key Responsibilities Deliver safe, evidence-based, patient-centred care aligned with professional standards, clinical guidelines, and local protocols Conduct patient assessments, develop care plans, deliver interventions, [. .. ] service delivery within wards, clinics, therapy services, or community settings (role dependent) Collaborate within multidisciplinary teams to support care coordination, escalation, discharge planning, and continuity of care Maintain accurate clinical documentation and handovers using approved documentation standards and clinical systems Uphold infection prevention and control (IPC) , medication safety (where applicable) , and clinical risk management practices Participate in quality assurance and continuous improvement activities, including audits, incident reporting, and corrective actions Ensure compliance with applicable German healthcare quality and safety [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
CRA II/ Senior CRA
• Frankfurt am Main
Work-Life-Balance
CRA II/ Senior CRA-Germany-office or remote ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] we 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 innovative treatments and therapies What You Will Be Doing: Conducting site qualification, [. .. ] 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 field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Biocair
Logistics Coordinator (Customer Care Coordinator)
• Hamburg
[. .. ] orders and enquiries and ensure that customer interactions are handled in a pro-active and professional manner at all times. Manage the end to end shipment process for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] research samples, clinical trials medicines and other pharmaceutical and healthcare related products, on a worldwide basis Ensure correct and timely completion of all after shipment tasks Develop and maintain a close relationship with existing and potential clients by understanding needs, providing high levels of accurate and timely communication, ensuring complete satisfaction with the service provided and identifying service level improvements. Liaise with suppliers to confirm documentation requirements, plan appropriate route solutions and obtain timely updates on live shipments. Develop a thorough knowledge of the Biocair supplier network and supplier capabilities to effectively plan routes that meet customer requirements. Ensure all Dangerous Goods shipments are correctly classified, have the correct documentation and that the route solution is [. .. ] and guide all that we do each day. The successful candidate will be expected to operate in line with them as we strive to be the provider of choice for specialist logistics solutions to the global scientific community; based on the highest levels of care, expertise and precision; enabling our customers to retain absolute focus on research and development. In return we offer: Between 45, 000-50, 000 per annum, depending on experience Pension Life Assurance (as part of a pension) [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Cordis
Professional Education (Prof Ed) Specialist Germany
• Hamburg
[. .. ] country based on Cordis educational strategy Coordinates faculty, center of references, participants, logistics, and on-site execution in collaboration with local support team. Ensures full compliance and complete, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] audit-ready documentation. Responsibilities Educational needs and planning Assess country training needs to educate HCPs and improve patient outcomes. Build and maintain a country Prof Ed calendar aligned to educational priorities. Prepare activity briefs, agenda, objectives, and expected clinical outcomes for each event. Manage the local Prof Ed budget within approved limits and reconcile on time. Faculty, centers of reference, and content Map and maintain a list of key opinion leaders (KOLs) , speakers, and reference centers by specialty. Propose faculty and Co Es per activity. Adapt approved regional [. .. ]
Neu Job vor 5 Std. bei Mindmatch.ai gefunden
Medical University of Vienna
PhD-Position (m/f/x)
• AT- 9 Wien
Jobticket Work-Life-Balance
[. .. ] Ph D-Position (m/f/x) (with immediate effect) . This is a contract for a duration until 31.8. 2028. The Pulmonology Laboratory at the Medical University of Vienna conducts [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical and basic research focusing on purinergic signaling in common lung diseases. Purinergic signaling influences all aspects of inflammatory processes and immune defense. Our research focuses on the pulmonary immune system to achieve reliable and lasting immune control in inflammatory lung diseases and successful anti-tumor immunity. Further information can be [. .. ] cell lines using CRISPR-Cas9 and episomal vectors In vitro and ex vivo assays to understand disease mechanisms Isolate and cultivate primary cells from tissue biopsies Processing tissue samples Precise documentation of experiments Your Profile A masters degree in a relevant field such as genetics, microbiology, molecular biology, or biotechnology is required Experience with mouse models and FELASA certification are advantageous Experience with cell culture, ELISA, cloning, PCR, q RT-PCR, Western blot, immunohistochemistry, and/or flow cytometry is required Well-organized, [. .. ] nursery or holiday activities Comprehensive training and development program Counselling services as required Health measures for prevention and health promotion Employee events (events for networking and celebrating as well as specialist presentations) Accessibility and commitment to diversity and inclusion The minimum monthly salary for this position (Uni-KV, Verw Gr. B1) is currently Euro 2.832, --gross (14x per year) on a part-time basis and may be increased by taking into account relevant previous experience and other salary components [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
Documentation Design Control Specialist (m/w/d) Medical Devices
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
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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 107 offene Stellenanzeigen für Clinical Documentation Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Documentation Specialist Jobs?
Aktuell suchen 33 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:
- Ciliatech (6 Jobs)
- GULP experts united (6 Jobs)
- Hire Resolve. com (4 Jobs)
- Antal Sp. z o. o. (3 Jobs)
- Novanta (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Documentation Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Documentation Specialist Jobs werden derzeit in Bayern (12 Jobs), Nordrhein-Westfalen (8 Jobs) und Berlin (8 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Documentation Specialist Jobs?
Clinical Documentation Specialist Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
