Clinical research associate Jobs in Ingelheim Am Rhein
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Clinical research associate • ingelheim am rhein
Zuletzt aktualisiert: vor 4 Tagen
Responsibilities : The employee shall provide Relocation Readiness Program services for Army Community Service.ACS uses Standard Operating Procedures for the various parts of its mission in order to...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Für die Unterstützung laufender klinischer Studien suchen wir eine erfahrene freiberufliche Clinical Research Coordinator (CRC), die Studienprojekte eigenständig und professionell begleitet.Die Tät...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Looking for a freelance opportunity where you can make an impact on technology from the comfort of your home? If you are dynamic, tech-savvy, and always online to learn more, this part-time flexibl...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen)
Clinical Child Psychologist / Psychotherapist.Kaiserslautern / Ramstein-Miesenbach, Wiesbaden, Böblingen (Stuttgart).Ongoing recruitment – Apply anytime.
Joy Center Family Institute is a multidiscip...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle.Our expertise spans full-service clinical development, project-based support, strategi...Mehr anzeigenZuletzt aktualisiert: vor 8 Tagen
Clinical Research Associate I
AbbVieWiesbaden, Hesse, Germany Supports in the in-house organization management and execution of projects to ensure the clinical trials are conducted recorded and reported in accordance with the protocol federal regulations and ...Mehr anzeigenZuletzt aktualisiert: vor 6 Tagen
HI-TRON Clinician Scientist Fellowship
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Army Community Service Assistant
Ladgov CorporationWiesbaden, DEQuick Apply
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Clinical Support Specialist - Rheinland-Pfalz, Teile Hessens und Baden-Würtemberg (7175)
Guided SolutionsRheinland-Pfalz, Teile Hessens und Baden-Würtemberg Our customer is a leading medical technology company that offers minimally invasive medical devices worldwide.As a family business, our customer strives to provide the best outcome for patients and...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Associate Director Procurement CDMO
BioNTech SEMainz, Rhineland-Palatinate, Germany Mainz, Germany | full time | Job ID : 10703.We are seeking a dynamic and experiencedAssociate Director Procurement CDMO / CMOto join our Global Procurement team.
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Study Nurse
Velocity Clinical ResearchWiesbaden, Hessen, GermanyQuick Apply
Online Data Research - German - Remote
TELUS Digital, MainzHomeoffice
Quick Apply
HI-TRON Clinician Scientist Fellowship
Deutsches Krebsforschungszentrum (DKFZ)Mainz The German Cancer Research Center (DKFZ) is one of Europe’s largest cancer research centers.Research for a life without cancer" is the mission of our world-class scientists and all our team m...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
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Senior Scientis t (m / f / d ), Preclinical Development ...Mehr anzeigenZuletzt aktualisiert: vor 4 Tagen
Wirtschaftsprüfer (m / w / d)
Bull Research ConsultingSchlangenbad, Hessen, Germany Unser Mandant ist eine unabhängige, inhabergeführte.Wirtschaftsprüfungsgesellschaft, die aus der Idee heraus entstanden ist,.
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Clinical Child Psychologist / Psychotherapist
Joy Center - Family InstituteWiesbaden, Hessen, GermanyQuick Apply
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TFS HealthScienceMainz, Rhineland-Palatinate, .DEQuick Apply
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Experienced Clinical Research Associate - Sign-On Bonus
MEDPACEMainz, United States Medpace is a full-service clinical contract research organization (CRO).We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mi...Mehr anzeigenZuletzt aktualisiert: vor 5 Tagen
Clinical Research Nurse 1
Georgetown University in QatarPre-Clinical Science Lower Level Georgetown University comprises two unique campuses in the nation’s capital.With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minute...Mehr anzeigenZuletzt aktualisiert: vor 25 Tagen
NexTPro – NextGen Training Programme IMB Research Placements for Bachelor & Master students (mfd)
Institute of Molecular BiologgyMainz, Rhineland-Palatinate, Germany Institute of Molecular Biology gGmbH (IMB).Centre of Excellence for Life Sciences funded by the Boehringer Ingelheim Foundation and the State of Rhineland-Palatinate and located within the campus o...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Clinical Research Associate I
AbbVieWiesbaden, Hesse, GermanyVor 6 Tagen
StellenbeschreibungSupports in the in-house organization management and execution of projects to 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 AbbVie 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 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. Ensures safety and protection of study subjects. Supports and / or conducts (accompanied) site qualification initiation interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations Good Clinical Practices (GCPs) ICH Guidelines and AbbVie Standard Operating Procedures (SOPs) and business processes if applicable. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas with appropriate supervision Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members. Appropriately escalates serious or outstanding issues. Facilitates Quality Assurance Audit processes as indicated. Ensures regulatory inspection readiness at assigned clinical sites. Reports monitoring activities and study site conduct accurately and completely. Prepare and submit written reports both monitoring and administrative with appropriate supervision. Keep management informed of study progress through periodic updates. Supports with Clinical Trial Application submissions including relevant informed consent local changes and translations into local language as required. Supports remote monitoring if and as applicable. Assists in study budget preparation and clinical study agreement execution including ensuring necessary payments are made according to executed agreements. Negotiates investigator / hospital agreements with stakeholders. Maintains and completes own expense reports as per local and applicable guidelines. Supports new and innovative processes and technologies to increase the quality productivity and efficiency of Clinical Operations and conserve overall departmental operating costs.
Qualifications :
- Appropriate life-science or healthcare-related qualification or experience or equivalent work experience.
- One year of clinically-related experience in a medical profession pharmaceutical or diagnostic company is preferred. Current knowledge and understanding of 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 within the assigned function.
- Strong analytical and conceptual capabilities interpersonal skills and ability to communicate with clarity. Ability to address study-related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
- Demonstrated business ethics and integrity.
- with a diverse work environment where you can have a real impact
- with an open corporate culture
- with an attractive salary
- with an intensive onboarding process with a mentor at your side
- with flexible work models for a healthy work-life balance
- with a corporate health management that offers comprehensive health and exercise programs
- with company social benefits
- with a wide range of career opportunities in an international organization
- with top-tier attractive development opportunities
- with a strong international network
What we offer you :
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more :
Work :
Yes
Employment Type : Full-time
Key Skills
CSS,Cloud Computing,Health Education,Actuary,Building Electrician
Experience : years
Vacancy : 1