PRINCIPAL INVESTIGATOR AND RESEARCH STAFF Sample Clauses

PRINCIPAL INVESTIGATOR AND RESEARCH STAFF. 2.1. Institution represents that it is entitled to and will procure the services of the Principal Investigator to act as Principal Investigator and shall ensure the performance of the obligations of the Principal Investigator set out in the Agreement.
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PRINCIPAL INVESTIGATOR AND RESEARCH STAFF. Institution represents that it is entitled to and will procure the services of the Principal Investigator to act as Principal Investigator and shall ensure the performance of the obligations of the Principal Investigator set out in the Agreement. Institution represents that the Principal Investigator holds the necessary registration and has the necessary qualifications, expertise, time and resources to perform the Clinical Trial. The Principal Investigator is made aware of the obligations applicable to the Principal Investigator set out in this Agreement and acknowledges his/her acceptance of said obligations by co-signing this Agreement. The Institution shall notify the Sponsor if the Principal Investigator ceases to be employed by or associated with the Institution or is otherwise unavailable to continue as Principal Investigator, and shall use all reasonable endeavours to find a replacement capable of continuing the Clinical Trial without undue delay and acceptable to both the Sponsor and the Institution, subject always to the Institution’s overriding obligations in relation to Clinical Trial Subjects and individual patient care. The Institution’s proposal for the Principal Investigator’s replacement shall not be rejected unreasonably by the Sponsor. If no mutually acceptable replacement can be found the Sponsor and the Institution may each terminate this Agreement pursuant to clause 12 below. The Institution shall procure and shall ensure that the Principal Investigator procures the performance of the obligations of the Research Staff as set out in this Agreement. All matters, terms and payment of compensation, benefits and other conditions of engagement of any nature for the Principal Investigator and any member of the Research Staff used in the Clinical Trial shall be solely a matter between the Institution and such individuals, regardless of whether such individuals are considered employees, agents or independent contractors of the Institution. The Institution will take appropriate steps to inform each such person of his/her obligations hereunder and to obtain his/her agreement to abide by the terms and conditions of this Agreement. The Institution represents that the Principal Investigator is free to participate in the Clinical Trial and there are no rights which may be exercised by or obligations owed to any third party which might prevent or restrict the Principal Investigator’s performance of his/her obligations set out in this Agreement. Subjec...

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