Investigator - Jobs

investigator-sponsored research proposals Contributes to the development of educational programs and materials Referral Site Support Work closely with other field-based employees and head-office staff to proactively support and improve the interaction between referral and Cell Therapy sites nationally Scientifically liaise with relevant referral sites...

proper and ethical interactions between PDT Global Medical Affairs personnel and external stakeholders Planning, designing and managing PDT global medical Advisory Boards as appropriate Providing medical review and approval of Investigator Initiated Research (IIR) proposals and other grants through the grant approval process Leading design and...

international teams, reporting directly to the Manufacturing System Lead. Key responsibilities include training personnel both virtually and on-site, managing training assignments, creating and tracking trainee requests, and communicating curricula updates. Additionally, the role involves certifying investigators and serving as an Administrator for the...

For informal inquiries, please contact the Principal investigator, Dr. Lucy Kinski (). Funded by the European Union (ERC, INCONEX, Grant No. 101163258). Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Research Council Executive Agency.

einschließlich der Betreuung der Prüfstellen vom Pre-Monitoring bis zum Abschlussbesuch Sicherstellung der Datenintegrität durch sorgfältige Pflege der Prüfstellenunterlagen und die Einhaltung relevanter Vorschriften (MDR) und Richtlinien (ISO 14155, ICH-GCP, DoH) Vorbereitung und Teilnahme an Investigator-Meetings, Organisation des rechtzeitigen...

submissions, Investigator’s Brochures (IBs), safety reports, and publications Support data generation activities including External Grant Proposals (EGPs) and post-marketing research Lead the publication plan and support Investigator Initiated Studies (IIS) as needed Compliance & Medical Governance Ensure medical accuracy and...

Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable. Participates in investigator meetings as vital. May help to identify potential investigators in collaboration with the...

(Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required. Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites...

Defense Meetings Attend and presents at Investigator’s Meetings Qualifications BSRT, RN, LPN, and/or equivalent degree Licensed specialist in relevant technology; CNMT required (Certified Nuclear Medicine Technologist). Minimum 5 years’ experience in the specified technology: Nuclear Medicine, Molecular imaging, etc.

Planung und Realisierung von Evidenzgenerierungsplänen, darunter lokale klinische Studien, Real-World-Evidence-Projekte und Investigator-Initiated Trials. Budgetverantwortung: Verwaltung des medizinischen Evidence Budgets für die zugeordneten Produkte. Globale/Regionale Repräsentation: Vertretung Österreichs in globalen Evidence Gap Planungsmeetings...

payers medical departments Owns medical content at congresses in Austria, including satellite symposia and other continuous medical education activity Supports investigator-initiated trial process in Austria and works closely with the EMEA and global team to ensure consistency Acts as Medical Device Consultant (Medizinprodukteberater) according to MPG ...

Collaborative team player with strong abilities to operate independently 11) Willing & able to travel domestically and internationally, as required (up to 40%) Responsibilities: Collaborate with Company Stakeholders to execute company objectives into successful clinical trials, investigator-sponsored studies, etc. Overall responsibility for design...

Communication of the clinical value of the TA products to population-health/formulary decision makers (outcomes Liaisons, as applicable) Providing high-quality, accurate, balanced and directed information to key customers and stakeholders in response to unsolicited requests for information, supports investigators in IIR submissions,

Key Responsibilities: Organizing and supervising clinical study: Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review BoardsResearch...

Top-notch environment with the ideas, projects, resources, infrastructure, collaborations, and mindset for ground-breaking research. Excellent track record of past postdocs who have become internationally successful principal investigators, professors, entrepreneurs. Strong focus on disease biology and translational research: