Common use of Study Staff Clause in Contracts

Study Staff. Institution 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 to initiation, will be evidence of acceptance this provision.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

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Study Staff. Institution 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 and Principal Investigator 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 to initiation, will be evidence of acceptance this provision.

Appears in 1 contract

Samples: Clinical Trial Agreement

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Study Staff. Institution 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 Principal Investigator 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 to initiation, will be evidence of acceptance this provision.

Appears in 1 contract

Samples: Clinical Trial Agreement

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