Part-Time Studies Sample Clauses

Part-Time Studies. 5.2.5.1 The selection of Employees to instruct in Part-Time Studies shall be subject to the final approval of the Employer. 5.2.5.2 In carrying out this responsibility, the following procedures shall be followed: 5.2.5.2.1 Where the course or courses to be taught fall within the area of expertise of a teaching Department of the Institute, that Department will be expected to select and recommend a candidate or candidates. 5.2.5.2.2 The opportunity to instruct in courses described in Article 5.2.5. 2.1 will first be offered to the Employees of that teaching Department for new or replacement positions. 5.2.5.2.3 Where the teaching Department concerned cannot recommend a suitable instructor for the course, the Part-Time Studies Department shall post the position internally, and apply the procedure in Articles 5.2.5.1 and 5.2.5.2. 5.2.5.2.4 Where the courses do not fall within the area of expertise of a teaching Department of the Institute the selection of candidates will be made by the Employer. 5.2.5.2.5 The opportunity to instruct in courses described in Article 5.
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Part-Time Studies. In cases where the Employer requires an Employee’s skills to be upgraded in a specific area of service, and where training for the said upgrading is not available outside of the business hours, time off, with pay, for lectures will be allowed to staff who wish to enroll for a single course directly related to their work, during working hours, with the approval of the Executive Director.
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Related to Part-Time Studies

  • Clinical Studies The animal and other preclinical studies and clinical trials conducted by the Company or on behalf of the Company were, and, if still pending are, to the Company’s knowledge, being conducted in all material respects in compliance with all Applicable Laws and in accordance with experimental protocols, procedures and controls generally used by qualified experts in the preclinical study and clinical trials of new drugs and biologics as applied to comparable products to those being developed by the Company; the descriptions of the results of such preclinical studies and clinical trials contained in the Registration Statement and the Prospectus are accurate and complete in all material respects, and, except as set forth in the Registration Statement and the Prospectus, the Company has no knowledge of any other clinical trials or preclinical studies, the results of which reasonably call into question the clinical trial or preclinical study results described or referred to in the Registration Statement and the Prospectus when viewed in the context in which such results are described; and the Company has not received any written notices or correspondence from the FDA, the EMA, or any other domestic or foreign governmental agency requiring the termination, suspension or modification of any preclinical studies or clinical trials conducted by or on behalf of the Company that are described in the Registration Statement and the Prospectus or the results of which are referred to in the Registration Statement and the Prospectus.

  • Project Timeline The Project Timeline establishes a start and end date for each Phase of the Project. Developed during the Initiate & Plan Stage and revised as mutually agreed to, if needed, the timeline accounts for resource availability, business goals, size and complexity of the Project, and task duration requirements.

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