Represent the company and the organization adequately to the customers and other external parties. Base all actions on Credo. Protect the rights of others, protect privacy and company assets, particularly information as the key asset. Conduct business in line with the HCC, company policies and procedures, including applicable SOPs, always having the ethical aspect in mind. Maintain adequate communication with relevant parties within and outside the company Comply with ICH-GCP and all applicable local laws and regulations. Actively follow trainings to ensure adequate qualification for performing job-related tasks. Report (suspicion of) fraud or scientific/ethical misconduct as appropriate. Regularly update information in applicable systems and templates. Contribute to the development and improvement of departmental procedures and processes and templates in the scope of the companys effort towards continuous quality improvement. Maintain quality standards and timelines that are consistent with business needs.
Requirements:
Description Responsible for global execution of a trial, supervising the delegated activities necessary for the planning, start-up, execution and closure of a clinical trial. 8 Years of experience needed.
NumberOfPositions: 1 Minimum Education: 4-Year College Degree Career Focus 1: Science/Biotech Career Focus 2: Healthcare/Medical
