Unser Recruiting Team steht Dir gerne zur Verfügung: - Annette Lauterbach, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
Unser Recruiting Team steht Dir gerne zur Verfügung: - Annette Lauterbach, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
Unser Recruiting Team steht Dir gerne zur Verfügung - Svjetlana Grajic, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
Unser Recruiting Team steht Dir gerne zur Verfügung - Svjetlana Grajic, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
BWI GmbH sucht in eine/n Lead IT Expert DevOps & Platform Engineering (m/w/d) (ID-Nummer: 13756518)
Sopra Steria sucht in eine/n Lead Expert Master Data Management / Logistik im Bereich Defence (m/w/d) (ID-Nummer: 12906212)
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.
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.
Unser Recruiting Team steht Dir gerne zur Verfügung: - Annette Lauterbach, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
Unser Recruiting Team steht Dir gerne zur Verfügung: - Annette Lauterbach, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
Ihr Ansprechpartner Herr ROLAND NOLL Kontakt empiricus GmbH - Agentur für IT Experten & Executives Nördliche Hauptstrasse 16 69469 Weinheim +49 151 27021735 +49 151 27021735 roland.noll@empiricus.eu
Unser Recruiting Team steht Dir gerne zur Verfügung: - Annette Lauterbach, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
Unser Recruiting Team steht Dir gerne zur Verfügung: - Annette Lauterbach, Senior Expert People Management #Telefon +4969566083050 #E-Mail bewerbung@infomotion.de
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.
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.