Clinical Project Manager
il y a 2 semaines
**Company Description**
As part of the world’s leading testing, inspection and certification company, you share the benefits of our stability and growth; secure employment in a financially stable, Swiss-based company; a proud heritage that has been making the world a better, safer place for over 140 years; and a global, multicultural, and multinational organization.
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.**
As 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.
**Qualifications** What 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 Information** What we can offer you**:
- A truly 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?
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