Study director Sample Clauses

Study director. For each study, a scientist or other professional of appropriate education, training, and experience, or combina- tion thereof, shall be identified as the study director. The study director has overall responsibility for the technical conduct of the study, as well as for the interpretation, analysis, documenta- tion, and reporting of results, and rep- resents the single point of study con- trol. The study director shall assure that:
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Study director. 3.1 Biocept shall appoint a “Study Director” to be responsible for each SOW. The Study Director shall coordinate performance of the Research Support and Services related to a SOW with a representative designated by Institution, which representative shall have responsibility for coordinating performance of the SOW for Institution. The Study Director and Institution’s representative shall be named in each SOW.
Study director. 1.2.1 RGI shall appoint a study director ("Study Director") to be responsible to oversee the completion of each Study by RGI. The Study Director shall coordinate performance of the applicable Study with a representative designated by GSK ("GSK Representative"), which GSK Representative shall have responsibility over all matters relating to the performance of such Study on behalf of GSK.
Study director. Contractor will appoint a "Study Director" to be responsible for the Study, and Sponsor will appoint a "Technical Representative" (AOAC RI Managing Director) to be responsible for the Study. Contractor's Study Director will coordinate performance of the Study with Sponsor's Technical Representative, who shall have the responsibility for all matters related to the performance of the Study on behalf of Sponsor. Contractor shall be entitled to rely upon representations and statements made to Contractor by Sponsor's Technical Representative.
Study director. F o r e a c h s t u d y , a scie n t i s t o r o t h e r p r ofessio n a l of a pp r op x x x x x xx u c a t io n , t r a i n i n g, a n d expe r ie n ce, o r co m bi n a- t io n t h e r eof, s h a ll be ide n t ified a s t h e s t u d y di r ec t o r . T h e s t u d y di r ec t o r h a s ove r a ll r espo n s ibili t y fo r t h e t ec hn ic a l co n d u c t of t h e s t u d y , a s well a s fo r t h e i n t e r p r e t a t io n , a n a l y s i s, xxx u m e n t a- t io n , a n d r epo r t i n g of r es u l t s, a n d r ep- r ese n t s t h e s i n gle poi n t of s t u d y co n- t r ol. T h e s t u d y di r ec x x x x x x ll a ss ur e t h a t :
Study director. WIL shall appoint a study director to be responsible for each Study (the “Study Director”). The Study Director will coordinate performance of the Study with the Sponsor’s designated representative, which representative shall have responsibility over all matters related to performance of the Study on behalf of Sponsor. WIL will not change the Study Director without the prior approval of Sponsor, which approval shall not be unreasonably delayed, conditioned, or withheld.
Study director. The Study will be conducted under the direction (,,,,,,,,,,,,,,,,),. as the study director (the "Study Director"). By signing this Statement of Work, the Study Director agrees to be bound by the terms and conditions of this Statement of Work and the Agreement to the extent that such terms and conditions relate to the Study Director. The Study Director hereby acknowledges receiving and reading a copy of the Agreement.
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Study director. Covance will appoint a Study director (“Study Director”) to be responsible for the completion of the Study by Covance. The Study Director will coordinate performance of the Study with a representative designated by Sponsor (“Sponsor Representative”), which representative shall have responsibility over all matters relating to performance of the Study on behalf of Sponsor. Unless otherwise agreed in the Protocol, all communication between Covance and Sponsor regarding the conduct of the Study pursuant to the Protocol shall be addressed to or routed through the Study Director and Sponsor Representative, directly. Covance may substitute Study Directors during the course of the Study.

Related to Study director

  • Director An Approved User who is generally a senior IT official of the Requester with the necessary expertise and authority to affirm the IT capacities at the Requester. The IT Director is expected to have the authority and capacity to ensure that the NIH Security Best Practices for Controlled-Access Data Subject to the NIH GDS Policy and the Requester’s IT security requirements and policies are followed by all of the Requester’s Approved Users.

  • Executive Committee (A) The Executive Committee shall be composed of not more than nine members who shall be selected by the Board of Directors from its own members and who shall hold office during the pleasure of the Board.

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