ING Deutschland sucht in eine/n HR Expert Performance & Reward (w/m/d) (ID-Nummer: 13673444)
The Team Data Science & Advanced Analytics – with departments in Frankfurt, Philadelphia, Milan, Madrid, Athens, Warsaw and Beijing as well as a network of more than 300 experts worldwide - is the global competence center for statistics and data science at IQVIA. Data Science & Advanced Analytics is responsible for developments of the statistical procedures and methods used for quality assurance processes, data imputations, data projections, forecasting and many other for healthcare panel data including pharmacy sales, ecommerce data, hospital consumption, physician level prescriptions and longitudinal anonymized patient level data.
ING Deutschland sucht in eine/n Customer Journey Expert / Product Owner Customer Onboarding – Business Banking (w/m/d) (ID-Nummer: 13677892)
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts at study sites and with client representatives. Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.
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 at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.
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: University Degree in life science or other scientific discipline or apprenticeship in health care.Minimum of two years of on-site monitoring experienceKnowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment.Good command of German and English.Flexibility to business travel up to 60% of working time.Driver’s license class B.
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 at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).
Octapharma Biopharmaceuticals GmbH sucht in eine/n Group Associate Expert Neutralization Testing (m/w/d) (ID-Nummer: 13725564)
Experte (m/w/d) Luftfracht Export Consol Internationale Sendungen bündeln. Prozesse steuern. Logistik bewegen. Sie kennen die Abläufe im Luftfracht-Export und fühlen sich besonders im Consol-Geschäft zuhause?
PwC Strategy& (Germany) GmbH sucht in eine/n Thought Leadership Expert (w/m/d) (ID-Nummer: 13724732)
ING Deutschland sucht in eine/n Process Expert Accounting & Reporting – Treasury (w/m/d) (ID-Nummer: 13677914)
Zur Verstärkung unseres Human Resource – Payroll Teams suchen wir Sie zum nächstmöglichen Termin als Senior Payroll Expert (m/w/d) Arbeitsort: Flexibel an einem unserer JLL Corporate Standorte mit der Möglichkeit hybrider Arbeitsgestaltung (Büro und Homeoffice).
ING Deutschland sucht in eine/n Product Development Expert (w/m/d) KMU-Lending (ID-Nummer: 13670026)
FAIR • ERFAHREN • TRANSPARENT Als Experten für IT-Personal und kaufmännische Fachkräfte im Rahmen der Arbeitnehmerüberlassung sowie im Dienstvertrag, unterstützen wir namhafte nationale und internationale IT-Unternehmen.
FAIR • ERFAHREN • TRANSPARENT Als Experten für IT-Personal und kaufmännische Fachkräfte im Rahmen der Arbeitnehmerüberlassung sowie im Dienstvertrag, unterstützen wir namhafte nationale und internationale IT-Unternehmen.
Innerhalb unseres Analytics & Consulting Teams beraten wir mit unseren Commercial Analytics Experten Unternehmen der Pharma- und Healthcare‑Industrie in markt- und vertriebsstrategischen Fragestellungen. Unsere Expert:innen entwickeln für unsere Kunden maßgeschneiderte Lösungen – von Markt‑ und Wettbewerbsanalysen über Marktforschung und Forecasts bis hin zu Marktstrategien, Vertriebsdesign, Kundensegmentierungen sowie Performance-Messungen.
Your responsibilities might include: 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)) that track site compliance and performance within project timelines.Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.Assist with periodic review of study files and completeness.Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.Act as a mentor for less experienced Clinical Trial Coordinators and assist with training and onboarding of new colleagues.May serve as subject matter expert for business processes or lead Clinical Trial Coordinators study teams.May participate in departmental quality or process improvement initiatives.
Sopra Steria Next sucht in eine/n Experte CFO-Advisory Public Sector (m/w/d) (ID-Nummer: 13163202)
We are looking for an exceptional Board-Certified physician to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development.The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and especially in the areas of Gene Therapy/Gene Editing, who will be a champion for CAGT across IQVIA.The key remit of the role is drive growth of the IQVIA CAGT portfolio through scientific and clinical expertise.