Ihre Zukunft beginnt heute Die Arbeitswelt von morgen braucht Experten wie Sie – Menschen mit dem Mut, Neues zu gestalten. Bei JLL finden Sie nicht nur einen Job, sondern eine Berufung, die Sie persönlich und beruflich erfüllt.
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
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 - 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
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).
Unsere Benefits Bei OPITZ CONSULTING profitierst du auch von einem Netzwerk an exzellenten Experten, Autoren und Konferenzsprechern, mit denen du dich über aktuelle Themen da draußen, aber auch über Herausforderungen auf deinem aktuellen Projekt austauschen wirst.regelmäßigen internen Community-Veranstaltungen zum Wissensaustausch oder um mit Kolleg*innen an gemeinsamen Themen für die eigene Weiterentwicklung oder die des Unternehmens zu arbeiten.vielfältigen Fort- und Weiterbildungsmöglichkeiten im Rahmen einer persönlichen Karriereplanung.einem individuellen Gehalts- und Arbeitszeitmodell und der Vereinbarkeit von Beruf und Familie.Absicherung bei Krankheit: wir bieten u.a. bis zu sechs Monate LohnfortzahlungAbsicherung im Alter: eine betriebliche Altersvorsorge, die wir aufstocken.Mobilitätslösungen: wir bieten eine grüne Firmenwagenregelung sowie ein JobRad.
Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits on medical devices trials.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), ISO 14155 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.Mentoring less experienced team members, acting as subject matter expert for specific topics or additional tasks might be included.
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).
Deutsche Post DHL Global Business Services Senior Expert “Project Manager for Digital Business Process Design” in the Digitalization@GBS program (non-managerial, non-pay-scale employee) Brief description of Digitalization@GBS: The Digitalization@GBS program is a large-scale digital transformation program that aims at greatly improving Deutsche Post DHL GBS’ services focusing on both enriching customer experience and reducing operating costs.