Common use of Investigator Obligations Clause in Contracts

Investigator Obligations. Investigator agrees to devote his/her best efforts to accurately and efficiently perform the work required under this Agreement, which efforts shall include but are not limited to the following: (i) exercise of independent medical judgment as to the compatibility of each Study patient with the Protocol requirements; (ii) notification of Chiltern and Sponsor, if required of any deviations from or failure to comply with the Protocol; (iii) promptly replying to any questions from Chiltern or Sponsor regarding any matter related to the Study; (iv) promptly notifying Chiltern of any significant changes that occur at any time during the Study which may affect Investigator or Institution’s ability to conduct the Study, including but not limited to, changes in personnel involved in the Study (b)

Investigator Obligations. Investigator agrees to devote his/her best efforts to accurately and efficiently perform the work required under this Agreement, which efforts shall include but by are not limited to the following: (i) exercise of independent medical judgment as to the compatibility of each Study patient with the Protocol requirements; (ii) notification of Chiltern Xxxxxxxx and Sponsor, if required of any deviations from or failure to comply with the Protocol; (iii) promptly replying to any questions from Chiltern Xxxxxxxx or Sponsor regarding any matter related to the Study; (iv) promptly notifying Chiltern Xxxxxxxx of any significant changes that occur at any time during the Study which may affect Investigator or Institution’s ability to conduct the Study, including but not limited to, changes in personnel involved in the Study Study; (b)

Investigator Obligations. Investigator agrees to and will ensure that Research Staff devote his/her her/their best efforts to accurately and efficiently perform the work required under this Agreement, which efforts shall include but by are not limited to the following: (i) exercise of independent medical judgment as to the compatibility of each Study patient with the Protocol requirements; (ii) notification of Chiltern Covance and Sponsor, if required of any deviations from or failure to comply with the Protocol; (iii) promptly replying to any questions from Chiltern Covance or Sponsor regarding any matter related to the Study; (iv) promptly notifying Chiltern Covance of any significant changes that occur at any time during the Study which may affect the Investigator or Institution’s ability to conduct the Study, including but not limited to, changes in personnel involved in the Study Study. (bd)

Investigator Obligations. Investigator agrees to will devote his/her best efforts to accurately and efficiently perform the work required under this Agreement, which efforts shall include but are not limited to the following: (i) exercise of independent medical judgment as to the compatibility of each Study patient with the Protocol requirements; (ii) notification of Chiltern and Sponsor, CRO and EC/IRB, if required required, of any deviations from or failure to comply with the Protocol; (iii) promptly replying to any questions from Chiltern Sponsor or Sponsor CRO regarding any matter related to the Study; (iv) promptly notifying Chiltern Sponsor and CRO of any significant changes that occur at any time during the Study which may affect Investigator or Institution’s ability to conduct the Study, including but not limited to, changes in personnel involved in the Study Study. (bd)