Clinical Project Manager

Job title:

Clinical Project Manager

Company

SGS

Job description

Company DescriptionAt SGS, you can choose.First of all, out of our various vacancies.However, SGS also gives you another choice.
Do you choose to expand or to enrich? We are not only looking for colleagues who can go into depths of their discipline. We are equally as much looking for colleagues who we call ‘connectors’, people who can connect our diversity to our services. To each other. And this way, enrich our business.SGS is the world’s leading inspection, verification, testing and certification company. We’re also the benchmark worldwide for quality and integrity. And that makes us very proud. This can only happen thanks to almost 100 000 colleagues worldwide, with more than 1650 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures.
Our coworkers build their own way inside the company, the services and the expertise.SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. SGS Life Sciences has also expertise in the quality control of pharmaceuticals.Grow in a company that is the home of global knowledge and expertise; that operates in a wide range of countries, services and sectors; and that offers you endless opportunities to learn, grow and fulfill you potential!In the spirit of continued growth, we are currently looking for a Clinical Project Manager.Job DescriptionAs Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects You will manage the project as such that the sponsor’s expectations are met within the constraints of the budget allotted to the project.You may also be involved in the pre-award process, the development of the project budget and related documents as well as client meetings, including bid defense meetings, if applicable.You will develop and manage the overall project planning and implementation, and you will be the primary liaison between the sponsor, the SGS project team, vendors and the site participating in the study throughout the lifecycle of the project.You will perform general supervision of the project and will liaise with the coordinating team members of the different parties involved in the execution of the project, in order to ensure the assigned trial is conducted in accordance to the contract and in compliance with 1) the applicable regulatory requirements, 2) the pre-defined procedures, 3) the applicable quality standards and 4) the mutually accepted work scope, study protocol and timelines.You will work pro-actively with the study team members to identify potential issues that might impact the execution of the project and/or the budget in any way and will provide contingencies to accommodate the needs of the assigned project.QualificationsWhat do you need to be successful?

• You have obtained a university degree, MSc, Pharm D, or PhD in life sciences/medical background.
• You have at least 2 years of experience in a clinical trial management role, having managed phase 1, 2 and /or 3 clinical trials in a pharmaceutical or biotech company or another CRO from set up to close out.
• ICH/GCP and MS Project do not have any secrets for you.
• You are fluent in English. Do you also speak another language? Great! That can be an asset!
• You are willing to travel (domestic and international)

Furthermore, you can recognize yourself in the following character traits:

• Professional: you bring quality, excellence, and ownership to everything you do
• Responsible and results-oriented: you have a sense of accountability for business results
• Committed: you bring your whole self to work with passion and focus
• Driven and eager: you are curious, flexible, and ambitious to learn from a global network
• Open to learning: from the range of different skills, backgrounds, and behaviors around you
• Capable of taking ownership and being independent
• Ambitious: you always challenge yourself to continuously improve and be the best you can be

Additional InformationWhat we can offer you:

• A rewarding career, working at the highest level of international standards for quality, safety and integrity
• The chance to share our growth and stability.
• Continuous learning from the best experts in the industry
• The chance to expand and enrich your career
• Professional and personal growth
• Experiences and opportunities across the global business

Do you want to be part of this?We are looking forward to hearing from you!
Send us your story and your resume via the apply button and maybe you will soon join us for work and coffee breaks. Still have questions? Heidi Aerts can give you more details about the job ( ).

Expected salary

Location

Mechelen, Antwerpen

Job date

Thu, 30 Jan 2025 07:50:42 GMT

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