30 Jobs für Clinical Study Assistant
Stellenangebote Clinical Study Assistant Jobs
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
• München
[. .. ] active 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Clinical Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner on a site level. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure delivery and [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Contract Clinical Research Associate
• 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 personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• 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 personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
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 personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
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 personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• 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 personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with an intensive onboarding [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• 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 assures timely submission of data, including appropriate reporting and [. .. ] appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Community College
Nursing Faculty (Instructor/ Assistant Professor/ Associate Professor/ Professor)
• Berlin
WHITE MOUNTAINS COMMUNITY COLLEGE NURSING FACULTY (INSTRUCTOR/
ASSISTANT PROFESSOR/ ASSOCIATE PROFESSOR/ PROFESSOR) ANNUAL SALARY (DETERMINED BY FACULTY LEVEL TO WHICH ASSIGNED) : INSTRUCTOR LEVEL: 49, 383-57, 639 ASSISTANT PROFESSOR [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] LEVEL: 53, 265-62, 374 ASSOCIATE PROFESSOR LEVEL: 57, 639-67, 546 PROFESSOR LEVEL: 65, 207-77, 041 INSTRUCTOR LEVEL SCOPE OF WORK : To educate students in [. .. ] with all college, system, state and federal rules and regulations. Other duties as assigned. MINIMUM QUALIFICATIONS : Education: Masters degree from a regionally accredited college or university with a major study in the field of nursing. Experience: Two years of teaching experience in nursing, or two years of experience directly related to the field of nursing. License/ Certification : Must possess current or active Registered Nurse license in New Hampshire. Must meet the continuing education requirements by the Board of Nursing [. .. ] college appointing authority. DISCLAIMER STATEMENT: These class specifications are descriptive of general duties and are not intended to list every specific function of these class titles. Position requires travel to clinical site locations. To be considered for this position, please complete the online application at https:/ / For more information, please contact WMCC is an equal opportunity employer and does not discriminate on the basis of race, creed, color, religion, ancestry or national origin, age, sex, sexual orientation, gender identity and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Fraunhofer- Gesellschaft
Unsolicited Application as Student Assistant (all genders)
• Leipzig
Werkstudenten
[. .. ] professional home for scientists, engineers, laboratory technicians, and administrative staff who work together in the service of health. Are you looking for an opportunity to work as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a student research assistant during your studies? Then you ve come to the right place At Fraunhofer IZI, we regularly mentor committed talents who want to conduct cutting-edge research with us. Be part of change At our institute, our employees delve into exciting projects and develop individual products and services for our clients, [. .. ] range of treatments in the future and give patients new hope. Together with our partners, we at the Fraunhofer IZI are driving forward the implementation of these pioneering approaches in clinical practice. Infectious diseases pose a constant challenge to global health-for humans and animals. To counteract these threats, we at Fraunhofer IZI are researching the mechanisms of disease transmission and development as well as innovative diagnostic and therapeutic approaches. Our infectious disease pathology team works closely with international partners to [. .. ] can find an overview of our business areas and departments here. What you contribute You are an enrolled student, preferably in life sciences, engineering, medicine or a related field of study. Ideally, you have already gained some experience through internships, vacation jobs or working student positions in the field you are interested in, but this is not a must. In any case, please always include a short cover letter with your application in which you explain your motivation for working as [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Hays Professional Solutions GmbH
• Dresden
Angebote von Zeitarbeitsunternehmen
[. .. ] bei der Erstellung und Weiterentwicklung standardisierter Arbeitsanweisungen (SOPs) und sicherheitsrelevanter Dokumente Ihre Qualifikationen: Medizinische Dokumentationsassistenz/ Studium der Naturwissenschaften/ CRA/ Fachangestellte für Medien- und Informationsdienste oder einem Gesundheitsberuf [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (Gesundheits- und Krankenpfleger, Study Nurse, MTA, PTA oder MFA) GCP Zertifikat und Kenntnisse von medizinischen Grundbegriffen Erfahrungen bei der Organisation von klinischen Studien wünschenswert Sehr gute Kommunikationsfähigkeiten, Flexibilität, organisatorisches Geschick und die Bereitschaft zur Teamarbeit Kenntnisse in der Med DRA Kodierung sind von Vorteil Sehr gute Kenntnisse der deutschen und englischen Sprache in Wort und [. .. ]
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-[. .. ] up and monitor studies, complete reports and maintain documentation Submitting protocol, consent documents for ethics/ IRB approval, as well as preparing regulatory submissions Balancing sponsor generated queries Taking responsibility for study cost efficiency Preparation and review of study documentation and feasibility studies for new proposals Potential to assist in training and mentoring fellow CRAs You are: 18 months of experience in clinical trials Degree in medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
Experienced Clinical Trials Assistant (m/w/d) , preferable based in Hamburg
• Frankfurt am Main
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client s project team in the execution of clinical trials. Joining the team provides the opportunity [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer the exciting opportunity to join the FSP team as Experienced Clinical Trials Assistant (m/w/d) in full-time and work in a combination of office and home-office preferable in the Hamburg area. RESPONSIBILITIES Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g. , Trial Master File (TMF) [. .. ]
Job vor 7 Tagen bei JobMESH gefunden
Thermo Fisher Scientific
• Baden- Wurttemberg
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description
Assistant CRA-Germany 2 Year Fixed Term contract At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on a global scale. Join our colleagues in bringing our Mission to life-enabling our customers to make the world healthier, cleaner and 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 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 [. .. ] will perform remote site management and monitoring activities on assigned project (s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and company procedural documents by reviewing study data from various sources remotely. You will contact study sites to collect study documentation, resolve issues and request outstanding information. A day in the Life: Develops and maintains a close and collaborative communication with the site staff. Actively discusses protocol conduction, enrollment rates and strategies, open issues, EDC completion and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Assistant CRA (m/f/d)
• Karlsruhe
Work Schedule Standard (Mon-Fri) Environmental Conditions Office
Assistant CRA-Germany 2 Year Fixed Term contract At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global scale. Join our colleagues in bringing our Mission to life-enabling our customers to make the world healthier, cleaner and 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 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 [. .. ] will perform remote site management and monitoring activities on assigned project (s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and company procedural documents by reviewing study data from various sources remotely. You will contact study sites to collect study documentation, resolve issues and request outstanding information. A day in the Life: Develops and maintains a close and collaborative communication with the site staff. Actively discusses protocol conduction, enrollment rates and strategies, open issues, EDC completion and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
PSI CRO
Principal Lead Data Manager
• München
Führungs-/ Leitungspositionen
[. .. ] employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Acts as primary communication point for project teams and company [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] departments regarding clinical data management. Acts as primary communication point for clients/ vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, e CRf/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/ Patient profiles generation and delivery Maintains and QCs e TMF. Maintains and QCs Data Management working files. Participates in preparation [. .. ] and client/ third-party audits/ inspections of Data Management. Participates in follow-up on and resolution of audit findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/ departmental level. Qualifications College or University degree or equivalent combination of training and experience [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Karlsruhe
Assistant CRA-Germany At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale. We provide our teams with the resources needed to achieve [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] individual career goals while taking science a step beyond through research, development and delivery of life-changing 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. Our global Clinical department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. We offer [. .. ] will perform remote site management and monitoring activities on assigned project (s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and company procedural documents by reviewing study data from various sources remotely. Develops and maintains a close and collaborative communication with the site staff. Actively discusses protocol conduction, enrollment rates and strategies, open issues, EDC completion and queries, as well as any other topic or indicator associated to project status and site performance. Completes/ tracks/ follows up [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Global Trial Associate (GTA) - Global Clinical Operations Leadership Development Program 2026
• Neuss, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https:/ / Job Function Job Function: R D Operations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Job Sub Function: Clinical Trial Support Job Category: Professional All Job Posting Locations: Beerse, Antwerp, Belgium, Breda, Netherlands, Copenhagen, Istanbul, Turkey, Madrid, Spain, Neuss, North Rhine-Westphalia, Germany, Paris, le-de-France, France, Prague, Czechia, Solna, Stockholm County, Sweden, Warsaw, Masovian, Poland Job Description The GCO Leadership Development Program consists of 12 months of [. .. ] GTAs will be placed in either the LTM or SM role depending on business need and skill set of the GTAs. Responsibilities Provide administrative and logistical support to Clinical Trial Assistant (CTAs) , SM and/or LTM in tracking progress of the trial, management of study data, budget, organizing meetings, mailing and correspondence, materials, drug distribution and other relevant tasks as appropriate in adherence to relevant SOPs, policies, and local regulatory requirements. Support the local study team in performing site feasibility and/or country feasibility. Collaborates with the Global Project Team, e. g. Clinical Trial Manager [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Director Clinical Operations
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Select how often (in days) to receive an alert: Mainz, Germany; London, United Kingdom full time Job ID:9757 About the Role: As Director
Clinical Operations, you will lead clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trial teams to ensure compliance with regulatory standards and drive successful study execution. Your leadership will be pivotal in resource planning, team development, and strategic decision-making to support Bio NTechs delivery of high-quality oncology programs. You will collaborate within a dynamic environment that values innovation and excellence, playing a vital role in advancing our mission to improve patient outcomes Your Contribution: [. .. ] CROs and vendors while contributing to strategic sourcing decisions for clinical trials A Good Match: University degree or experience in a medical profession (e. g. , Nurse or Medical Technical Assistant) Profound knowledge of relevant legislation and international guidelines (ICH-GCP) for clinical research projects 12+ years of experience in project management, regulatory submissions, and global study organizations, including 6+ years leading global clinical development teams Proficiency in software tools such as Word, Excel, Power Point, MS Project Strong organizational and [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Berlin
Overview WHITE MOUNTAINS COMMUNITY COLLEGE NURSING FACULTY (INSTRUCTOR/
ASSISTANT PROFESSOR/ ASSOCIATE PROFESSOR/ PROFESSOR) Annual Salary (determined by faculty level to which assigned) : INSTRUCTOR LEVEL: 49, 383 57, 639 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ASSISTANT PROFESSOR LEVEL: 53, 265 62, 374 ASSOCIATE PROFESSOR LEVEL: 57, 639 67, 546 PROFESSOR LEVEL: 65, 207 77, 041 INSTRUCTOR LEVEL SCOPE OF WORK : To educate students in [. .. ] Complies with all college, system, state and federal rules and regulations. Other duties as assigned. MINIMUM QUALIFICATIONS Education: Masters degree from a regionally accredited college or university with a major study in the field of nursing. Experience: Two years of teaching experience in nursing, or two years of experience directly related to the field of nursing. License/ Certification: Must possess current or active Registered Nurse license in New Hampshire. Must meet the continuing education requirements by the Board of Nursing to [. .. ] college appointing authority. DISCLAIMER STATEMENT: These class specifications are descriptive of general duties and are not intended to list every specific function of these class titles. Position requires travel to clinical site locations. To be considered for this position, please complete the online application at https:/ / . For more information, please contact WMCC is an equal opportunity employer and does not discriminate on the basis of race, creed, color, religion, ancestry or national origin, age, sex, sexual orientation, gender identity [. .. ]
Job am 18.01.2026 bei Jobleads gefunden
Manager Clinical Trials
• Mainz, Rheinland- Pfalz
Select how often (in days) to receive an alert: Mainz, Germany; London, United Kingdom full time Job ID:9860 The
Clinical Trial Manager (CTM) is responsible for supporting the Sr. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Global CTM and/or Associate Director Clinical Trials with the execution of a clinical trial (s) or leading the execution of smaller trials, mainly with regard to operational and administrative aspects. Your main responsibilities are: Support in preparation of regular status [. .. ] budget Opportune contact with Project Manager and Associate Director Clinical Operations in case of divergences from the project plan Oversight on project timelines and deliverables Set-up or oversight of study related documents such like Trial Management Plan, Monitor Manual, etc. Contribution to and review of study core documents, e. g. , synopsis, investigators brochure, patient informed consent documents etc. Coordination of project activities with other internal departments or external vendors from start-up to close out of a clinical trial [. .. ] to starting project activities, oversight. What you have to offer: Natural/ life sciences or medical background (university degree or experience in a medical profession such as Nurse or Medical Technical Assistant or Pharmaceutical Technical Assistant) Profound knowledge and experience in relevant legislation and international guidelines (ICH-GCP) for the performance of clinical research projects Minimum 3 years of experience in project management, regulatory submissions, monitoring of clinical trials or clinical trial coordination with practice in project planning and structuring Refined colloquial [. .. ]
Job am 22.12.2025 bei Jobleads gefunden
Principal Lead Data Manager
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Acts as primary communication point for project teams and company [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] departments regarding clinical data management. Acts as primary communication point for clients/ vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, e CRf/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/ Patient profiles generation and delivery Maintains and QCs e TMF. Maintains and QCs Data Management working files. Participates in preparation [. .. ] and client/ third-party audits/ inspections of Data Management. Participates in follow-up on and resolution of audit findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/ departmental level. Qualifications College or University degree or equivalent combination of training and experience [. .. ]
Job am 20.12.2025 bei Jobleads gefunden
• München, Bayern
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based
Clinical Trial
Assistant to join our Clinical Monitoring team. This position will work in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a team to accomplish tasks and projects that are instrumental to the companys success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Perform administrative duties in conformity with company policies and procedures; Provide day-to-day study support activities such as maintenance of project-related files, corresponding with study teams, etc. Coordinate and schedule meetings, provide meeting minutes; Maintain databases/ project specific status reports Support filing and quality control reviews of our internal regulatory filing system; Manage study supplies; Perform other administrative tasks as needed Qualifications A [. .. ]
Job am 19.12.2025 bei Jobleads gefunden
Medical Writer (m/w/d)
• Hannover, Niedersachsen
Beratungs-/ Consultingtätigkeiten
[. .. ] (for further information: benefit assessment of pharmaceuticals) as well as EU Health Technology Assessments (HTA) in collaboration with our clients Scientific and statistical analysis, interpretation, gap analysis, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and presentation of clinical study results Independent review of scientific literature and preparation and documentation of qualitative and quantitative analyses Collaboration in interdisciplinary, agile teams composed of clients and colleagues Application of stateoftheart, AIsupported technological solutions and New Work methods (e. g. , Design Thinking, SCRUM, Kanban) Active contribution to the continuous development of Kintiga [. .. ] events and much more Sounds good to you? Apply now We look forward to receiving your application, incl. Letter of application Complete certificates incl. high school diploma Janina Spottke Executive Assistant to the Managing Directors B. B. A. Hons. Fon: +49 511 64 68 14 0 Fax: +49 511 64 68 14 18 #J-18808-Ljbffr 73002116 [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Regulatory And Clinical Start Up Specialist (Biotech)
• München, Bayern
Regulatory And
Clinical Start Up Specialist (Biotech) Join to apply for the Regulatory And Clinical Start Up Specialist (Biotech) role at Progressive Direct message the job poster from Progressive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory and Start up Associate/ Specialist Responsible for oversight of assigned global clinical trials Review of regulatory submission documents and packages Support study teams as RA representative Preparation of responses to regulatory requests Support of regulatory interactions as applicable Negotiation of Budgets Contract Management Experience Requirements University degree or professional education e. g. Pharmaceutical/ Medical Technical Assistant with a minimum of 1-2 years professional experience preferably in pharmaceutical industry (an academic degree in natural sciences e. g. Bachelor would be an advantage) Fluent in written and verbal English Advanced knowledge and on-hands experience in using office software-e. g. MS Office Programs, SAP, Zoom, Teams [. .. ]
Job gestern bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to work [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer the exciting opportunity to join the team as Experienced Clinical Trial Coordinator (m/w/d) in full-time and work in home-office throughout Germany. [. .. ] medical or pharmaceutical field or office management. At least 2-4 years experience as Clinical Trial Coordinator or within another administrative role in clinical research, e. g. as Clinical Trials Assistant, Study Start-Up Assistant. Knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Study Assistant pro Jahr?
Als Clinical Study Assistant verdient man zwischen EUR 35.000,- bis EUR 55.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Study Assistant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 30 offene Stellenanzeigen für Clinical Study Assistant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Assistant Jobs?
Aktuell suchen 14 Unternehmen nach Bewerbern für Clinical Study Assistant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Study Assistant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Study Assistant Stellenangebote:
- Abb Vie (6 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- IQVIA (2 Jobs)
- PSI CRO (2 Jobs)
- Community College (1 Job)
- Fraunhofer- Gesellschaft (1 Job)
In welchen Bundesländern werden die meisten Clinical Study Assistant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Assistant Jobs werden derzeit in Bayern (3 Jobs), Hessen (2 Jobs) und Sachsen-Anhalt (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Assistant Jobs?
Clinical Study Assistant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
