129 Jobs für Clinical Quality Associate
Stellenangebote Clinical Quality 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
[. .. ] 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. [...]
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[...] , 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 [. .. ] project-related activities and administrative tasks within the ERC project You may contribute to teaching activities depending on interest and availability, in which case you participate in evaluation measures and in quality assurance. Your profile:Completed Ph D in economics, management, data science, or a closely related field Strong background in econometrics and empirical research methods Experience with large-scale data work and data integration Programming skills in Python, R, Stata, and SQL Interest in pharmaceutical innovation, patents, and the science of science Experience [. .. ]
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 [. .. ] help you gain experience in a wide variety of therapeutic areas. Responsibilities Performing site selection, initiation, monitoring and closeout visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance 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 [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Universität Wien
Scientific project assistant postdoc
• AT- 9 Innere Stadt
[. .. ] 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. [...]
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[...] , 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 [. .. ] project-related activities and administrative tasks within the ERC project You may contribute to teaching activities depending on interest and availability, in which case you participate in evaluation measures and in quality assurance. Your profile:Completed Ph D in economics, management, data science, or a closely related field Strong background in econometrics and empirical research methods Experience with large-scale data work and data integration Programming skills in Python, R, Stata, and SQL Interest in pharmaceutical innovation, patents, and the science of science Experience [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
IQVIA LLC
• AT- 9 Wien
Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech page is loaded # # Clinical Associate Regulatory Submissions, Austria, IQVIA Biotechlocations: Vienna, Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1522611 [...]
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[...] Clinical Associate Submissions Regulatory Homebased Austria IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all [. .. ] in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. You will also ensure adherence to standard operating procedures (SOPs) , Work Instructions, quality of designated deliverables and project timelines. You will prepare submission documents and submit to regulatory bodies. You will perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions, along with distributing completed documents to sites and internal project team members. You will [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
Biogen, Inc.
ICOE FA Associate Director Field Content Creation
• 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 [. .. ] 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 [. .. ] a unified medical voice and consistent alignment with therapeutic area vision, strategy, and customer insights. Your work will directly impact the effectiveness of field teams by providing them with high-quality, compliant, and engaging scientific content. Who You Are: You are a strategic thinker who thrives in collaborative environments. You have a knack for translating complex scientific data into accessible, engaging content. Your attention to detail ensures high standards of accuracy and integrity in all materials you produce. You are passionate [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
ICON
• 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 welcome you [...]
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[...] to join us on our mission to shape the future of clinical development. As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes. What You Will Do: Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
Clinical Research Associate (CRA)
• 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 [. .. ] 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, and timely delivery. If you enjoy working in a dynamic clinical research environment and want to contribute beyond routine monitoring while maintaining a strong focus on sitelevel excellence, you will feel right at home at Gouya Insights. What you will be responsible for: Perform clinical monitoring activities in [. .. ]
Job am 26.03.2026 bei Mindmatch.ai gefunden
IQVIA
• 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 [...]
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[...] 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 [. .. ] areas and in covering projects in Austria, Germany and/or Switzerland. Responsibilities Performing site selection, initiation, monitoring and closeout visits. Supporting the development of a subject recruitment plan. Evaluating the quality and integrity of site practices in accordance 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. [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
Clinical Research Associate
• 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 [. .. ] monitoring plan and Teleflex procedures. Works cooperatively with Research Coordinators and Investigators to schedule and conduct monitoring visits including site qualification, site initiation, routine monitoring and site closure visits. Evaluates quality and integrity of site practices while escalating quality issues as appropriate. Works cooperatively with the Teleflex Clinical Studies project team members to prepare for monitoring visits, escalates significant findings during monitoring visits and proactively provides input on site performance. Adequately prepares for monitoring visits to ensure monitoring activities are organized, [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• 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-[. .. ] 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 support. Maintain accurate, timely, and complete TMF documentation, requesting updates as [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Clinical Research Associate (Eastern Europe) Growth Impact
• 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 [...]
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[...] 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
• AT- 9 Wien
[. .. ] and development location. Your main tasks and responsibilites Act as scientific Subject Matter Expert within the lifecycle management of blood plasma products Collaborate crossfunctionally with Productions Sites, [...]
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[...] Manufacturing Science Technology, Quality, Regulatory Affairs, Business Units and other R D areas Lead and scientifically guide continuous process optimizations, process transfers, root cause analyses of investigations, change 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 [. .. ] 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 am 11.12.2025 bei Jobleads gefunden
Medical Science Liaison Complement-Mediated Diseases
• München, Bayern
Medical Science Liaison Complement-Mediated Diseases Seniority level
Associate Employment type Full-time Job function Other Pharmaceutical Manufacturing At Sobi, each person brings their unique talents to work as a team [...]
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[...] and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes [. .. ] engagement, medical scientific projects and scientific communications. Key Responsibilities Identify, develop and maintain collaborative relationships with KOLs, scientific experts and other medical scientific stakeholders. Compile, analyze, prepare and deliver high quality medical pharmaceutical and scientific communications in line with defined communication plans. Create and execute stakeholder engagement plans, according to Sobis high standards. Support country Global Brand team in developing local medical tactics and provide input to Headquarter (HQ) / regional plans if relevant. Organize and set up scientific advisory boards [. .. ] , D. N. P. , Ph. D. , or M. D. / D. O. ) . Consideration will be given to candidates with an advanced health degree and extensive industry or clinical experience. Ability to understand and effectively communicate scientific information; respond to inquiries and address needs of key stakeholders. A minimum of 1 year of MSL experience. Demonstrated success managing internal/ external stakeholders and leading or influencing cross-functional teams in a matrixed environment including strong teamwork and collaboration. Proven track [. .. ]
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 [. .. ] processes and workflows for planning, scheduling, and tracking. Ensures that robust, realistic project plans are maintained and that regular, accurate communication is provided to stakeholders at all levels Ensures that quality reviews occur on schedule and according to procedure Leads change control procedure and ensures that project deliverables are completed within agreed cost, timescale and resource budgets are signed off Leads 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 [. .. ]
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 [...]
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[...] 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 [. .. ] 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 [. .. ] to ensure that the trials are being conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Veeva Systems
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 [...]
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[...] 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
PSI CRO
Clinical Research Associate/ Senior Clinical Research Associate
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
We are the company that cares for our staff, for our clients, for our partners and for the
quality of the work we do. A dynamic, global, mid-size company [...]
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[...] founded in 1995, we bring together more than 3, 000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description As a Senior/ Clinical Research Associate at PSI you will be involved in improving patients lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. Hybrid role in Munich/ Planegg or Home-based in Germany You will: Conduct and report all [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Abb Vie
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Ludwigshafen am Rhein, DE
Teilzeit
Work-Life-Balance
[. .. ] of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute [...]
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[...] to improving patients quality of 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 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 3 Tagen bei Jooble gefunden
Biontech
Associate Director Audit Management
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As
Associate Director Audit Management, you will play a pivotal role in ensuring the
quality and compliance of Bio NTechs
clinical trials and processes. As part of [...]
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[...] the Global Development Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Charles River Laboratories, Inc.
Shipping Receiving Associate
• Kreis Mettmann; Regierungsbezirk Düsseldorf; Westfalen Duesseldorf
Work-Life-Balance
[. .. ] characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks [...]
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[...] through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20, 000 biologic testing reports are sent each and over 200 licenses products are supported by [. .. ] client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of peoples lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on [. .. ]
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 [. .. ] 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 they arise. Manage risk and control measures to assure project quality. Analyze discrepancies between planned and actual results. Review and approve responses to [. .. ] 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. [. .. ] monitoring, 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 [. .. ]
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 [. .. ] 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 [. .. ] identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent [. .. ]
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 [. .. ] (speaking, writing) and good comprehension of English language where English is not the local language Excellent people skills and ability to work successfully in a matrixed team environment Dedication to quality in all work tasks and deliverables Ability to prioritize and manage multiple tasks as necessary, including during travel and monitoring visits Working knowledge of computer systems, applications, and operating systems Ability to travel up to 75 Possess a valid drivers license, as required 90137939 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical quality associate pro Jahr?
Als Clinical quality associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Quality Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 129 offene Stellenanzeigen für Clinical Quality Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Quality Associate Jobs?
Aktuell suchen 30 Unternehmen nach Bewerbern für Clinical Quality Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Quality Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Quality Associate Stellenangebote:
- IQVIA (4 Jobs)
- ICON (4 Jobs)
- Biontech (3 Jobs)
- Alimentiv (2 Jobs)
- Veeva Systems (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Quality Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Quality Associate Jobs werden derzeit in Bayern (24 Jobs), Berlin (17 Jobs) und Niedersachsen (14 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Quality Associate Jobs?
Clinical Quality Associate Jobs gehören zum Berufsfeld Qualitätswesen.
