261 Jobs für Clinical Quality Associate
Stellenangebote Clinical Quality Associate Jobs
Neu Job vor 5 Std. bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research
Associate (CRAs) and Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation [. .. ] departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities. Assist in vendor management activities as required per project. Perform review of visit reports for quality, compliance and appropriate site management. Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan. Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc. ) and inform clinical project team on progress. Contribute to financial project [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ] 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 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision. Ensures quality of data submitted from study sites and [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Stryker
• Regierungsbezirk Freiburg
Grow Your Career at Stryker as an
Associate Manager,
Clinical Data Science As an Associate Manager for Clinical Data Sciences, you will lead a diverse team of experts and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] collaborate with internal and external stakeholders to implement and execute Clinical Data Sciences initiatives for the Instruments division. This role involves driving operational planning, building technical infrastructure to support excellence in evidence communication, and integrating real-world data sources into Strykers clinical evidence strategy. You will provide leadership and mentorship to clinical expert staff, fostering development and ensuring high-quality deliverables that advance clinical intelligence across the organization. Establish the Clinical Data Sciences function at Instruments. Develop a strategy to grow the team and expertise to support business growth objectives. Lead and manage the Clinical Data Sciences team, which will leverage data from various sources to foster clinical evidence communication [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
CRA II/ Sr CRA-FSP-Germany (m/f/d)
• Homeoffice
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. The PPD FSP Solution: PPD s Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions. We cover customer needs on every level, [. .. ] within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience. A day in the Life: As a Clinical Research Associate, you will: Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects. Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. Perform and coordinate [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Frankfurt am Main
Homeoffice möglich
Join IQVIA as a CRA II/ Sr CRA (m/w/d) in our
Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex [. .. ] work on ground-breaking new medicine development. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out 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 on study sites and client representatives. Qualifications: [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
Clinical Research Associate/ Germany
• 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, and ISO 14155:2020. Key Responsibilities: Conduct monitoring activities including visit preparation, on-site 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, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
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 to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
Clinical Research Associate
• Mainz
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Clinical Research Associate. About this role As part of our FSP team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. This role is dedicated to one of our clients. This role is a full-time role based Germany. Key Responsibilities: Monitor clinical trial sites to ensure [. .. ] biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. #Together we make a difference Standort TFS Health Science, Mainz 74826186 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
Freelance CRA Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] 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 am 14.01.2026 bei Jooble gefunden
Adragos Pharma GmbH
Internship M A (f/m/d) starting June 2026 or later
• München
[. .. ] Microsoft Powerpoint and Excel know-how as well as a good portion of common sense. You are proficient in English, other languages are a plus. Contact Alina von [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Eyb HR Associate/ People Culture About us Adragos Pharma is a reliable Contract Development and Manufacturing Organization (CDMO) headquartered in Munich, Germany. We provide comprehensive development and manufacturing services for drug products, including sterile and non-sterile liquids, solids, and semi-solids. Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply. With production sites in Germany, France, Greece, Norway, Japan, and Switzerland, we ensure high-quality manufacturing across all stages of the drug development process. Founded in 2020, Adragos Pharma has rapidly grown through an ambitious buy build strategy, supported by FSN Capital. With a team of over 900 professionals, we are expanding our operations across Europe, North America, and Japan to become a global leader [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and 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. [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Project Associate (Oncology)
• Homeoffice
Work-Life-Balance
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 to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
• München
Führungs-/ Leitungspositionen
The
Associate Director, Medical Affairs Dermatology (Atopic Dermatitis) , is part of the Medical Affairs Team and represents his/ her area of responsibility towards external and internal stakeholders. Owing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to his/ her profound understanding of the respective treatment area and extensive network the Associate Director Medical Affairs Dermatology establishes and fosters collaborations with external partners and provides a bridge between clinical development, medical affairs and the commercial organization at a senior mastery level. He/ she provides critical insights into the countrys medical affairs plan for the respective disease areas, ensuring that it complements the companys development plan and adheres to the highest scientific standards. Constantly build and maintain expertise in the [. .. ] that scientific results stemming from the national IIR projects are acknowledged within the scientific community in a timely manner Provides oversight and contributes to the preparation and delivery of high-quality content and all educational and medical communication materials (e. g. planning for medical society presence, abstracts and publications) Streamlines product communication, works with external and internal resources on the development of materials (for internal and field/external use) and medical event planning Participates in relevant cross-functional working-groups and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Research Associate (CRA) - Oncology
• Homeoffice
Work-Life-Balance
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 to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
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 to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Trials Assistant-Oncology
• Homeoffice
Work-Life-Balance
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 to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Clinical Research Associate
• München
This is what you will do: The
Clinical Research
Associate (CRA) has local responsibility for the delivery of the studies at their assigned sites and is an active [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] participant in the local study team (s) . The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO) , Study Start-Up (SSU) manager, Clinical Study Assistant [. .. ] Proactively identifying and ensuring timely resolution to study-related issues and escalates them as appropriate. Training, supporting, and advising Investigators and site staff in study-related matters, including Risk Based Quality Management (RBQM) principles. Development of recruitment plans with each site and managing and supporting enrollment to ensure sites and studies meet enrollment milestones. Document recruitment barriers and implement mitigation plans. Ensure agreed monitoring KPIs are observed and remain within the agreed quality acceptable ranges (Action Items aging, SDV metrics, Data [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Talkspace Remote Therapist Roles
Evening/ Weekend Contract Therapist
• Homeoffice
[. .. ] committed to fostering a diverse, equitable, inclusive, and belonging-centered workplace where everyone can thrive while making a difference in mental health. Want to help over two million [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] people receive quality mental healthcare? Come join our mission to get therapy into the hands of everyone We re looking for a part-time, contract Therapist (Independent Contract Provider) who is passionate about reaching individuals who need mental healthcare but lack easy access to it. This role is perfect for those seeking the [. .. ] the secure (HIPAA compliant) Talkspace platform Conduct client sessions using video, audio, and live messaging services Respond to asynchronous client messages each week, in a timely manner Complete your required clinical documentation after each client session Offer availability during evenings and/or weekends About you Current license to practice independently without supervision in your state (s) of licensure Note: Associate licensed providers who require supervision are not eligible for this role Individual professional malpractice liability insurance policy Individual NPI number Comfortable learning new online tools and technology Reliable internet connection and video-capable device Perks Clients Ready for You: Talkspace provides new client referrals Flexible Schedule: Set your own schedule [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Research Associate-Oncology
• Homeoffice
Work-Life-Balance
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 to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ] to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
Clinical Research Associate (Klinischer Monitor)
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and 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. [. .. ]
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 [. .. ] data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelors degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth k Nwledge of clinical trial processes, regulations, and ICH-GCP [. .. ]
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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 261 offene Stellenanzeigen für Clinical Quality Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Quality Associate Jobs?
Aktuell suchen 35 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:
- MEDPACE (25 Jobs)
- ICON (20 Jobs)
- Astra Zeneca (19 Jobs)
- IQVIA (10 Jobs)
- Wolters Kluwer (9 Jobs)
- Alimentiv (7 Jobs)
In welchen Bundesländern werden die meisten Clinical Quality Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Quality Associate Jobs werden derzeit in Bayern (22 Jobs), Sachsen-Anhalt (18 Jobs) und Berlin (18 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Quality Associate Jobs?
Clinical Quality Associate Jobs gehören zum Berufsfeld Qualitätswesen.
