Global Trial Lead

15-11-2018 beerse
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: 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.

vos atouts

- 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

chef de projet / manager (m/f)
type de job
temps plein, freelance
type contrat
jobs fixes immédiat
informations de contact
Laurence Teerlynck 03 201 39 26
03 201 39 26