Study Staff Sample Clauses

Study Staff. Institution, through Principal Investigator, shall be responsible for distributing a GDPR transparency notice to, and if required by Sponsor, for obtaining consent of, each Study Staff in order for Sponsor and its designees to process Study Staff personal data to the extent needed for the Study purposes. Such personal data shall at all times be processed in accordance with Data Protection Laws. Sponsor (or Sponsor’s designee) shall provide the transparency notice and any required consent to Institution in a form approved by Sponsor for distribution. If consent is required by Sponsor, Sponsor will have discretion whether to accept the Study Staff signature on the Delegation of Responsibilities Log, provided by Sponsor prior 6.20. Personál studie: Zdravotnické zařízení prostřednictvím Hlavního zkoušejícího zodpovídá za předání oznámení o transparentnosti podle GDPR každému členovi Personálu studie, a pokud si to Zadavatel vyžádá, za získání souhlasu každého člena Personálu studie, aby mohl Zadavatel a jím pověřené osoby zpracovávat osobní údaje Personálu studie v rozsahu potřebném pro účely Studie. Tyto osobní údaje budou za všech okolností zpracovávány v souladu s Právními předpisy o ochraně osobních údajů. Zadavatel (nebo jím pověřená osoba) poskytne Poskytovateli zdravotních služeb oznámení o transparentnosti a případný požadovaný souhlas ve formě schválené Zadavatelem k předávání. Pokud bude Zadavatel požadovat souhlas, bude na jeho rozhodnutí, zda to initiation, will be evidence of acceptance this provision. přijme podpis Personálu studie v záznamu o delegování povinností, který Zadavatel dodá před zahájením, jako důkaz přijetí tohoto ustanovení.
Sample 1
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Study Staff. Institution, through Principal Investigator, shall supervise Study Staff in their performance of the Study and ensure that all Study Staff are qualified to perform the duties assigned to such person. Institution shall take reasonable steps to inform Study Staff of their obligations under this Agreement.
Sample 1
Study Staff. Site will ensure that all Study Staff have the medical, technical and/or laboratory expertise to conduct the Study and are available to support and carry out Site’s obligations under this Agreement. Further, Institution will ensure that before commencing any work on the Study, all Study Staff are subject to written obligations to Institution under which they (i) are bound to obligations of confidentiality and non-use with respect to Confidential Information (as defined below) that are consistent with the terms of this Agreement; and (ii) assign and otherwise effectively vest in Institution any and all rights that such Study Staff might otherwise have in the results of their work without any obligation of Sponsor to pay any royalties or other consideration to such Study Staff.
Sample 1
Study Staff. Sponsor and its designees shall process Study Staff personal data to the extent needed (i) to conduct the Study; (ii) to satisfy requirements under Applicable Laws, including review by regulatory authorities; and (iii) storage in databases for use in selecting investigators and institutions for future clinical trials.. 6.21.
Sample 1
Study Staff. All personnel performing services on the Study under the direct supervision and instruction of Institution and Investigator, including, but not limited to the Investigator, sub-investigators, study coordinators, study nurses, employees, agents and/or subcontractors of Institution.
Sample 1

Related to Study Staff

  • Principal Investigator The research will be under the direction of (“Principal Investigator”). If, for any reason, he/she is unable to continue to serve as Principal Investigator and a successor acceptable to both UHD and Sponsor is not available, this Agreement shall be terminated as provided in Section 7.

  • Collaboration Management Promptly after the Effective Date, each Party will appoint a person who will oversee day-to-day contact between the Parties for all matters related to the management of the Collaboration Activities in between meetings of the JSC and will have such other responsibilities as the Parties may agree in writing after the Effective Date. One person will be designated by Merck (the “Merck Program Director”) and one person will be designated by Moderna (the “Moderna Program Director,”) together will be the “Program Directors”. Each Party may replace its Program Director at any time by notice in writing to the other Party. Any Program Director may designate a substitute to temporarily perform the functions of that Program Director by written notice to the other Party. The initial Program Directors will be: For Moderna: [***] For Merck: [***]

  • Project Management Project Management Institute (PMI) certified project manager executing any or all of the following: • Development of Project Charter • Development of project plan and schedule • Coordination and scheduling of project activities across customer and functional areas • Consultation on operational and infrastructure requirements, standards and configurations • Facilitate project status meetings • Timely project status reporting • Address project issues with functional areas and management • Escalation of significant issues to customers and executive management • Manage project scope and deliverable requirements • Document changes to project scope and schedule • Facilitate and document project closeout

  • Office and Support Staff During the Employment Period, the Executive shall be entitled to an office or offices of a size and with furnishings and other appointments, and to exclusive personal secretarial and other assistance, at least equal to the most favorable of the foregoing provided to the Executive by the Company and its affiliated companies at any time during the 120-day period immediately preceding the Effective Date or, if more favorable to the Executive, as provided generally at any time thereafter with respect to other peer executives of the Company and its affiliated companies.

  • Project Team To accomplish Owner’s objectives, Owner intends to employ a team concept in connection with the construction of the Project. The basic roles and general responsibilities of team members are set forth in general terms below but are more fully set forth in the Design Professional Contract with respect to the Design Professional, in the Program Management Agreement with any Program Manager, and in this Contract with respect to the Contractor.

  • Project Manager The term “Project Manager” refers to the employee of the State who has been assigned responsibility for overseeing and managing the proper and timely implementation of the project.

  • Program Management 1.1.01 Implement and operate an Immunization Program as a Responsible Entity

  • Project Managers The JBE’s project manager is: [Insert name]. The JBE may change its project manager at any time upon notice to Contractor without need for an amendment to this Agreement. Contractor’s project manager is: [Insert name]. Subject to written approval by the JBE, Contractor may change its project manager without need for an amendment to this Agreement.

  • Training a. The employer, in consultation with the local, shall be responsible for developing and implementing an ongoing harassment and sexual harassment awareness program for all employees. Where a program currently exists and meets the criteria listed in this agreement, such a program shall be deemed to satisfy the provisions of this article. This awareness program shall initially be for all employees and shall be scheduled at least once annually for all new employees to attend.

  • Contract Management To ensure full performance of the Contract and compliance with applicable law, the System Agency may take actions including:

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