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description de la société
Do you believe in affordable healthcare? Are quality & safety your priority number 1? Then you'll feel comfortable in this company, who's one of the biggest pharmaceutical companies in the world.
As a Global Trial Leader you will play a major role in the creation of high level layouts for different departments! Just apply here for this challenging opportunity: firstname.lastname@example.org or 03 200 28 01.
description de la fonction
Do you want to help transform the way clinical trials are executed? Then you are the expert we are looking for!
- You will represent the company and the organization adequately to the customers and other external parties. - You will base all actions on Credo. - You will protect the rights of others; protect privacy and company assets, particularly information as the key asset. - You will conduct business in line with the HCC, company policies and procedures, including applicable SOPs, always having the ethical aspect in mind. - You will maintain adequate communication with relevant parties within and outside the company. - You will comply with ICH-GCP and all applicable local laws and regulations. - You will report (suspicion of) fraud or scientific/ethical misconduct as appropriate. - You will regularly update information in applicable systems and templates. - You will contribute to the development and improvement of departmental procedures and processes and templates in the scope of the company’s effort towards continuous quality improvement. - You will maintain quality standards and timelines that are consistent with business needs.
- You have excellent leadership and team player skills. - You have the ability to manage and support the activities of the Local trial and Site Managers and other local staff assigned to the trials for which responsible. - You have a passion for digital technologies and how these are implemented in clinical studies - You are able to organize multiple complex priorities and projects and use a range of techniques to identify and resolve trial-related problems. - You can understand and apply coaching theory and skills and select appropriate coaching structure to suit individual needs. - You are able to solve complex global trial-related situations. - You have good presentational and motivational skills. - You can understand and use a range of computer-based systems to track, monitor and report on investigational site and local trial activity and status. - You possess a comprehensive knowledge of and comply with Company SOPs, ICH-GCP, (where appropriate, global) and local national regulations. - You have experience and proficiency in the conduct and management of clinical trials. - You know how to cope with change and influence/motivate others to deal with change. - You have a thorough understanding of clinical drug development and regulatory procedures and processes within GCO. - You are proficient in English, both written and spoken.
You definitely need to apply if you're looking for a contract at Ausy, a project based contract or an opportunity as a freelancer, because it's all possible! As an answer to your high performance & flexibility, Ausy offers you an interesting salary package, with some nice extra's like:
- Meal vouchers of €7 - Net representation cost of €50 - DKV hospitalization insurance - Car + fuel card OR home-work compensation - 32 holidays - End-of-year bonus - ECO vouchers - Opportunities to follow trainings