Subinvestigators and Research Staff. Institution and Principal Investigator will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff (subinvestigators and research staff collectively referred to as “Research Staff”). Principal Investigator may delegate duties and responsibilities to Research Staff only to the extent permitted by Applicable Law (hereinafter defined) governing the Trial conduct, as described below.
Subinvestigators and Research Staff. Institution and Principal Investigator will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff.
Subinvestigators and Research Staff. Provider and Principal Investigator will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff (subinvestigators and research staff collectively referred to as “Research Staff”). Principal Investigator may delegate duties and responsibilities to Research Staff only to the extent permitted by Applicable Law (hereinafter defined) governing the Trial conduct, as described below. Sponsor may hold investigator meetings for scientific purposes relevant to the Trial, including, without limitation, training Research Staff and providing updates on material safety information. At the request of either CRO or Sponsor, the Principal Investigator and relevant Research Staff are encouraged to attend any such investigator meetings. Provider acknowledges that either CRO or Sponsor may reimburse expenses or provide travel and/or hospitality in direct connection with such meetings. For avoidance of doubt, any payments for services in connection with an investigator meeting, (e.g. presenting) shall be subject to a separate agreement.
Subinvestigators and Research Staff. Institution and Principal Investigator will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff (subinvestigators and research staff collectively referred to as “Research Staff”). Principal Investigator may delegate duties and responsibilities to Research Staff only to the extent permitted by Applicable Law (hereinafter defined) governing the Trial conduct, as described below. Principal Investigator is responsible for timely study specific training of research staff. 1.2. Spoluzkoušející a výzkumný personál. Zdravotnické zařízení a hlavní zkoušející zajistí, aby se na provádění klinického hodnocení jako spoluzkoušející a výzkumný personál podílely pouze osoby s odpovídajícím vzděláním a kvalifikací (spoluzkoušející a výzkumný personál jsou společně označováni jako „výzkumný personál”). Hlavní zkoušející může delegovat povinnosti a odpovědnosti na výzkumný personál pouze v rozsahu povoleném platnými zákony (definované níže) upravujícími provádění klinického hodnocení, jak je uvedeno níže. Hlavní zkoušející je odpovědný za včasné vyškolení výzkumného personálu odpovídající požadavkům na provedení studie.
Subinvestigators and Research Staff. Principal Investigator may delegate duties and responsibilities to subinvestigators or research staff (subinvestigators and research staff collectively referred to as “Research Staff”) who may be employees or contracted third parties only to the extent permitted by Applicable Law (hereinafter defined) governing the Study conduct, as described below. The Principal Investigator shall comply with ICH X0 X0, sections 4.2.5 and 4.2.6, and agrees to be responsible for supervising the Research Staff. Institution acknowledges that Principal Investigator will ensure that only individuals who are appropriately qualified and trained assist in the conduct of the Study, ensure the integrity of the Study-related duties and functions performed and any Study data generated by the Research Staff.
Subinvestigators and Research Staff. Principal Investigator will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Study as subinvestigators or research staff.
Subinvestigators and Research Staff. Institution and Principal Investigator will ensure that all personnel who assist in the conduct of the Trial, including subinvestigators (collectively, “Research Staff”) are appropriately trained and qualified.
Subinvestigators and Research Staff. Institution and Principal Investigator will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff (subinvestigators and research staff collectively referred to as “Research Staff”). Principal Investigator may delegate duties and responsibilities to Research Staff only to the extent permitted by Applicable Law (hereinafter defined) governing the Trial conduct, as described below. Sponsor and CRO hereby undertake not to conclude any other contract in connection with this Trial with any employee of the Institution, without having Institution´s prior written consent.
Subinvestigators and Research Staff. Institution will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff. 1.2. Pomocní vyšetrovatelia a výskumníci. Inštitúcia zabezpečí, aby pri výkone Skúšania v úlohe pomocných vyšetrovateľov a výskumníkov napomáhali len jednoTvci, ktorí sú správne vyškolení a kvalifikovaní.
Subinvestigators and Research Staff. Institution will ensure that only individuals who are appropriately trained and qualified assist in the conduct of the Trial as subinvestigators or research staff. Institution, through Principal Investigator, may delegate duties and responsibilities to subinvestigators or research staff only to the extent permitted by Applicable Law (hereinafter defined) governing the Trial conduct, as described below. In case of termination of the Pharmacy Services Agreement by the respective Team Member (Pharmacist), Institution will ensure, after it receives the copy of the written notice, the new Team Member (Pharmacist) who will assist in the conduct of the Trial.
