135 Jobs für Clinical Data Associate
Stellenangebote Clinical Data Associate Jobs
Job vor 4 Tagen bei Aktuelle TopJobs gefunden
Deutsche Rentenversicherung Baden- Württemberg
Sachbearbeiter/in Projektbüro (m/w/d)
• Karlsruhe oder Stuttgart
Sachbearbeiter/in Projektbüro (m/w/d) Deutsche Rentenversicherung Baden-Württemberg Karlsruhe oder Stuttgart Die Deutsche Rentenversicherung (DRV) Baden Württemberg ist einer der größten Regionalträger der gesetzlichen Rentenversicherung mit rund 3.600 Mitarbeitenden. Unsere Digitalisierungsabteilung stellt [...]
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[...] Anwenderinnen und Anwendern ein breit [. .. ]
Job vor 8 Tagen bei jobanzeigen.de gefunden
Universität Wien
Scientific project assistant postdoc
• 1010, Wien, Österreich
[. .. ] Statistics. About the project SUSTECH investigates how technological trajectories in chemistry and pharmaceuticals evolve, with a particular focus on the selection of hazardous versus sustainable innovations. The [...]
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[...] project combines large-scale data on chemical compounds and patents with computational chemistry and machine learning to generate novel insights into innovation processes and policy design. The Theory Testing Lab at the University of Vienna focuses on empirical analyses of pharmaceutical innovation, developing and leveraging large-scale datasets (e. g. , patents, clinical trials, molecular data) to study how innovation trajectories emerge and are shaped. The position offers the opportunity to contribute to internationally visible, frontier research. You will have the chance to help build and shape a high-impact interdisciplinary research group while working on your own research. The group is led by Prof. Stefan Wagner, who publishes in leading international journals and serves as Associate Editor at Management Science. Your responsibilities:As a Postdoctoral Research you will:Conduct independent and collaborative empirical research on pharmaceutical innovation and technological trajectories Build, manage, and analyse large-scale datasets (e. g. , patent data, clinical trials, molecular and firm-level data) Apply advanced econometric methods to study innovation processes and [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Homeoffice möglich
Join IQVIA as a
Clinical Research
Associate I or II (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. Youll enjoy the stability [...]
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[...] and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether youre just starting out or [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Collaborating with experts at study sites and with client representatives Depending on client model there might be remotemonitoring, involvement in study startup processes, specialization on therapeutic area (pharmaceutical product or medical devices) Mentoring of less experienced team members, support as subject matter expert for specific topics or additional [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Universität Wien
Scientific project assistant postdoc
• AT- 9 Innere Stadt
[. .. ] Statistics. About the project SUSTECH investigates how technological trajectories in chemistry and pharmaceuticals evolve, with a particular focus on the selection of hazardous versus sustainable innovations. The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] project combines large-scale data on chemical compounds and patents with computational chemistry and machine learning to generate novel insights into innovation processes and policy design. The Theory Testing Lab at the University of Vienna focuses on empirical analyses of pharmaceutical innovation, developing and leveraging large-scale datasets (e. g. , patents, clinical trials, molecular data) to study how innovation trajectories emerge and are shaped. The position offers the opportunity to contribute to internationally visible, frontier research. You will have the chance to help build and shape a high-impact interdisciplinary research group while working on your own research. The group is led by Prof. Stefan Wagner, who publishes in leading international journals and serves as Associate Editor at Management Science. Your responsibilities:As a Postdoctoral Research you will:Conduct independent and collaborative empirical research on pharmaceutical innovation and technological trajectories Build, manage, and analyse large-scale datasets (e. g. , patent data, clinical trials, molecular and firm-level data) Apply advanced econometric methods to study innovation processes and [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novamed
• AT- 6 Hengsberg
Teilzeit
[. .. ] is seeking an experienced Facilities Maintenance Manager to join our amazing team Job Title Facilities Maintenance Manager General Purpose of the Job Under the supervision of the [...]
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[...] Practice Administrator and Clinical Director the Facilities Maintenance Manager is responsible for the operation and maintenance of the Ambulatory Surgery Center (ASC) facilities, equipment and property. Oversees all buildingrelated activities. Performs overall housekeeping, building, grounds, safety, maintenance, custodial support, organization of events, ensuring that ASC operates efficiently by planning and directing building related services. [. .. ] meetings and educational trainings and activities as needed. Know, understand, and follow all HVSC policies and procedures. Performs any other duties as assigned. Qualifications High School Diploma or equivalent required. Associate degree (A. A. ) or equivalent from a twoyear college or technical school; or six months to one year related experience and/or training; or an equivalent combination of education and experience. Ability to perform duties under pressure and meet deadlines in a timely manner. Ability to effectively communicate with [. .. ] work as a team, interact with others in a professional/ pleasant manner and exercise problemsolving skills. Must be able to apply principles of logical thinking or define problems, collect pertinent data, establish facts, draw valid conclusions and initiate appropriate course of action. Advanced computer skills and proficiency in MS Word, Excel, and email required. Equal Employment Opportunity Work Force Diversity Our organization is an equal opportunity employer and will not discriminate against any employee or applicant for employment based on race, [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
oeh
(Associate) Principal Scientist (m/f/d) Bioinformatics Infrastructure Engineer, Agentic AI
• AT- 9 Wien
Homeoffice möglich
The position Computational Innovation (computationalinnovation) is a global organization with sites in Vienna, Biberach, London, and Ridgefield, focused on advancing AI and
data-driven scientific discovery. At our Vienna location, we [...]
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[...] are growing the Data Excellence team and are recruiting a Bioinformatics Infrastructure Engineer to design and operate robust, scalable bioinformatics data platforms while driving the enablement of agentic AI systems in scientific workflows. The role sits at the intersection of large-scale [. .. ] acted upon by autonomous AI agents. You will work closely with computational biologists, data scientists, and AI/ ML teams to support complex end-to-end workflows across large-scale omics, clinical, imaging, and phenotypic data domains. Tasks responsibilities Design, implement, and maintain scalable bioinformatics data infrastructure, including data models, storage, and compute environments, supporting the full data lifecycle from ingestion through downstream analytics. Engineer end-to-end data processing and integration pipelines for large and complex internal and external biomedical datasets [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
Biogen, Inc.
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] compliant with industry regulations and internal guidelines. Develop and maintain a comprehensive library of scientific and medical content, including presentations and slide decks, for field medical teams. [...]
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[...] Analyze and interpret clinical data and published real-world evidence to integrate into the scientific narrative. Stay current with the latest medical and scientific advancements in therapeutic areas and translate complex data into engaging content for field teams. Assess content impact and effectiveness; identify opportunities for improvement and optimization. Collaborate with I-Co E partners in [. .. ] genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. About This Role: As the ICOE FA Associate Director Field Content Creation, you will play a pivotal role within Biogens International Center of Excellence (ICOE) team, focusing on the development and delivery of essential medical content for country medical teams. You will be integral in executing medical launch readiness and advancing priorities in key European and Intercontinental markets [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
ICON
Clinical Research Associate
• AT- 9 Wien
Work-Life-Balance
Clinical Research
Associate-Remote-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. As a CRA I at ICON, you [. .. ] compliance with ICONs procedures, protocols, and regulatory requirements. Your Profile: University degree in medicine, science, or equivalent Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data Excellent written and verbal communication in English Good social skills enabling you to deal with queries in a timely manner Willingness to travel as required (approximately 60) What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
• AT- 9 Wien
Job Description
Clinical Research
Associate (CRA) at GOUYA INSIGHTS Are you an experienced Clinical Research Associate (CRA) looking to further strengthen your expertise in clinical trial execution? Gouya [...]
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[...] Insights is seeking a motivated and handson CRA to join our growing clinical operations team. In this role, you will be responsible for onsite and remote monitoring activities, ensuring protocol adherence, data integrity, and subject safety. You will work closely with investigational sites and internal teams to oversee regulatory documentation, ethics committee and hospital submissions at site level, and trial conduct in accordance with SOPs, ICHGCP, and applicable regulatory requirements. All activities are performed with a strong focus on quality, inspection readiness, [. .. ]
Job am 16.04.2026 bei Mindmatch.ai gefunden
Alimentiv
Clinical Research Associate I/ II Eastern Europe
• AT- 9 Wien
A
clinical research organization in Wien is hiring Clinical Research Associates (CRA I/ II and Senior) to support site management and ensure compliance with regulations. Responsibilities include conducting remote [...]
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[...] data reviews and providing operational support to Senior CRAs. Candidates must have an Honours Bachelor Degree and relevant experience, ranging from 1 to 3 years depending on the role. Offering a base salary and eligibility for performance-based bonuses, benefits include health and dental plans. J-18808-Ljbffr 88805762 [. .. ]
Job am 16.04.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
A leading healthcare company in Austria seeks a
Clinical Research
Associate (CRA) to conduct on-site and remote monitoring visits while ensuring compliance with regulatory standards. The ideal candidate [...]
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[...] will have a Bachelors or Graduate degree in life sciences and at least two years of relevant monitoring experience. Responsibilities include scheduling visits, evaluating data integrity, and preparing thorough Monitoring Visit Reports. Fluency in both German and English is required. The role offers a gross monthly salary starting at 3, 437. J-18808-Ljbffr 88805704 [. .. ]
Job am 26.03.2026 bei Mindmatch.ai gefunden
IQVIA
Clinical Research Associate 2 (m/w/d) , IQVIA Biotech, based in Austria
• AT- 9 Wien
Homeoffice möglich
Join IQVIA Biotech as a
Clinical Research
Associate 2/ CRA 2 (m/w/d) to work home-based throughout Germany, and preferably in the Munich or Hamburg area. You will enjoy [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the stability and resources of a leading, global contract research organization while gaining direct experience with our clients. This role promises to offer intentional career growth and [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts at study sites and with client representatives. Mentoring less experienced team members, support as subject matter expert for specific topics or additional tasks might be included. Qualifications University Degree in life science or other scientific discipline or apprenticeship in the health care field. Minimum of [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research
Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance [...]
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[...] with applicable regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate data accuracy and subject safety required by review of regulatory documents, medical records, reported data and device storage, if applicable. The CRA must be able to identify issues, present findings to the site staff, provide retraining if needed, provide problemsolving strategies and communicate findings to the study team and department management [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
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[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on our side-[. .. ] Research Associate I/ II Support/ conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance with SOPs, protocol, and GCP. Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
A leading
clinical research organization in Austria is seeking candidates for Clinical Research
Associate positions at various levels. The roles involve supporting site management through monitoring and initiation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] visits while ensuring data quality and compliance. Ideal candidates must hold an Honours Bachelors Degree with relevant experience ranging from 1 to 3 years depending on the level. The organization offers competitive compensation, including a base salary and performance bonuses, along with a comprehensive benefits package. J-18808-Ljbffr 83093352 [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Octapharma Austria
Senior Scientist (m/w/d) - Scientific Operations Services-R D Plasma
• AT- 9 Wien
[. .. ] requests, submissions and inquiries from internal and external stakeholders Manage, coordinate, perform and continuously improve multiple complex lab operations and analytical tasks Critically coach others in laboratory [...]
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[...] excellence, review experimental data and ensure highquality scientific interpretations and conclusions Prepare, review and present reports, presentations, and scientific insights in accordance with internal standards to both internal and external stakeholders Coach, mentor, and supervise Scientists, Associate Scientists, and technical staff, supporting their growth and development Your expertise and ideal skill set University degree (MSc or Ph D) in biotechnology, biochemical engineering, biochemistry, biology, pharmaceutical sciences, or a related discipline Minimum 58 years of relevant experience in biopharmaceutical R D, including industrial exposure in Gx P regulated setting Expertise [. .. ] with a proactive, resultdriven and collaborative mindset Proficient in German and English (oral + written) Your department-where you make an impact We, the Research Development department, conduct preclinical and clinical research to develop new products and ensure their safe and effective use throughout their overall lifecycle. Our ultimate focus in our daily work is on increasing patient health and safety. Thrive with us Company restaurant meal subsidy Training further education Health promotion Parking spaces and good public transport connections Company [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Calyx
• Berlin
We re on a mission to change the future of
clinical research. At Perceptive, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is [...]
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[...] to change the world but to do this, we need people like you. Key Responsibilities Project Management Owns resolution and decision-making for medium to complex studies, applying senior judgement to navigate [. .. ] cross-functional stakeholders to align on project scope, priorities, timelines, and dependencies, driving actions to keep delivery on track. People Management Where applicable manages and mentors a small number of Associate Project Managers and/or Project Managers by setting clear performance expectations and objectives, providing regular coaching and feedback and ensuring priorities and workload are balanced to meet project timelines and quality standards. Change Management Leads in the assessment, development, documentation and implementation of changes based on requests for change. Contribute [. .. ] may include status of site qualification, image processing, result reporting, and query management across all supported projects, and follow up with the applicable internal groups or imaging centres as needed. Data Management Provides oversight and coordination to resolve data reconciliation findings, partnering with Data Management, Sci Med and Operations to drive timely, compliant resolution. Drives proactive data quality monitoring and governance, ensuring outlier and trend reports are reviewed, actions are assigned, and follow-up is completed. Relationship Management Leads stakeholder engagement [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Senior CRA Germany Oncology
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Veeva Systems
• Berlin
Beratungs-/ Consultingtätigkeiten
Veeva is building the industry cloud for Life Sciences through software,
data, AI, and Business Consulting working together. Learn more about our products, vision and values, and status as [...]
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[...] a public benefit corporation on our website. Consulting is changing, and were not like other firms. Veeva Business Consulting was launched in 2019 and has grown quickly and organically to a global organization [. .. ] measuring tangible business value. R D Business Consulting supports biopharma, medtech, animal and consumer health customers with solving business problems across the R D value chain but also specifically within Clinical, Pharmacovigilance and Regulatory domains. You will be part of a global team delivering meaningful and high-impact projects with a variety of organisations from Top 20 Pharma to small/ mid-sized organisations. What Youll Do Lead project workstreams from end-to-end, ensuring the high-quality design and delivery of customer solutions Solve complex problems for Life Sciences leaders, leveraging Veevas unique data and software insights Mentor and manage Associate Consultants, overseeing their work and professional development within your workstream Drive practice growth by contributing to business development and internal IP creation Requirements Experience: 3+ years in Life Sciences Consulting (Business or Management Consulting preferred) Domain Knowledge: Proven expertise in Clinical Data/ Operations, Regulatory or Pharmacovigilance/ Drug Safety Analytical Rigor: [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Abb Vie
Project Data Manager/ Associate Scientist II (all genders) (full-or parttime, temporary for 18 months)
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Ludwigshafen am Rhein, DE
Teilzeit
Work-Life-Balance
[. .. ] life 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] together as Project Data Manager/ Associate Scientist II (all genders) Your tasks and responsibilities: Support cross-functional laboratory sample and data operations in all stages of Abb Vie clinical trials and in compliance with GCP/ GLP requirements Initiate, coordinate and revise documents for setting up projects/ services with vendors, for example on the external storage of clinical trial samples Support sample data curation, intake, reconciliation and transfer using bioanalytical LIMS and ELN software Support internal and external sample storage [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Indero
Project Manager II (Germany)
• Unstrut- Hainich- Kreis; Thüringen Thueringen
Description The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned
clinical trials. The project manager II oversees and [...]
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[...] coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs) , good clinical practices, regulatory and study-specific requirements. Project Manager II acts as the main line of communication to [. .. ] up timelines, and site contracting and budgeting. Collaborate with Regulatory Affairs to ensure timely submissions and completeness of essential documents prior to site initiation and throughout the study. Partner with Data Management to ensure CRF alignment with protocol and sponsor requirements, and that data review, query resolution, and database lock timelines are met. Quality and risk management Ensure assigned studies are audit ready at all times. Monitor the quality of study deliverables, (including vendor and Sub CRO deliverables) and address issues as [. .. ] functional departments, and senior management. Manage and report on recruitment status and highlight initiatives needed to meet recruitment timelines. Project team leadership Lead the core project team which may include: Associate Project Managers, Project Coordinators, Project Assistants. Ensure all team members have adequate training on the project. Work closely with vendors and the following internal teams to ensure all tasks and deliverables are completed on time, according to plans and according to applicable standards: Site Selection, Regulatory Affairs, Data Management, Clinical [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Allucent
Sr. Clinical Research Associate (Germany)
• Regierungsbezirk Köln; Westfalen Koeln
[. .. ] a last impact on patients worldwide. Together we. Find more information about our values. The role Bring your monitoring expertise to the forefront of innovation. We are [...]
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[...] looking for a Clinical Research Associate (CRA) to join our A-team. As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. [. .. ] and close-out visits. Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements. Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection. Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety. Activities around regulatory affairs, site activation and study-startup. Requirements To be successful you will possess: Youre an experienced CRA ready to take the next step with a company that truly values your expertise [. .. ]
Job vor 5 Tagen bei Jooble gefunden
CRA II Germany-eastern Germany (Leipzig, Halle, Berlin)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Biontech
Associate Director Translational Sciences (Infectious Diseases)
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
Jobticket
[. .. ] cross-functional Translational sub-team you will collaborate with a Translational Lead on the development and implementation of program-specific, integrated biomarker strategies from Ph1 to licensure, in alignment with [...]
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[...] clinical development objectives through contributing to the translation of preclinical results and approaches to clinical biomarker strategies supporting efficient clinical development of the assigned infectious disease assets. Your main responsibilities are: Contributing to the translation of preclinical results and approaches to clinical biomarker strategies supporting efficient clinical development of the assigned infectious disease assets through data-driven decision making and regulatory compliance Partnering with clinical, technical, and scientific colleagues to contribute to the overall biomarker strategy and assist in its execution Provides biomarker and translational contributions to the integrated development plan, clinical development plan, and to regulatory study-or program-related documents such as clinical trial [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
Clinical Research Associate-Germany
• Deutschland Deutschland, DE
The
Clinical Research
Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical data associate pro Jahr?
Als Clinical data associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 135 offene Stellenanzeigen für Clinical Data Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Associate Jobs?
Aktuell suchen 26 Unternehmen nach Bewerbern für Clinical Data Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Associate Stellenangebote:
- Biontech (5 Jobs)
- IQVIA (4 Jobs)
- ICON (4 Jobs)
- Optimapharm d. o. o. (4 Jobs)
- Alimentiv (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Data Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Associate Jobs werden derzeit in Bayern (25 Jobs), Berlin (14 Jobs) und Niedersachsen (12 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Associate Jobs?
Clinical Data Associate Jobs gehören zum Berufsfeld Medizintechnik.
