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Project Coordinator Ii, Medical Devices

3 semanas atrás


Oeiras, Portugal Labcorp Tempo inteiro

If you are a **CRA**, **In-House CRA**/**Centralized Monitor** or **Project Coordinator** who is on their **early years** of experience in clinical research, realize that your true passion lies in Project Management, and find yourself in one of these scenarios:

- **_ Crave to have a bigger picture_** of your studies, beyond your country sites,
- **_ Want to stop travelling_**, or are not convinced the next step in your career is becoming a travelling CRA,
- Already are a Project Coordinator, but **can´t**_ progress your career _**to actually become a PM yourself,
- You are not benefiting from a learning environment that allows you to **_fulfill your potential_** at the right time and accelerate your career...

then there is no better moment to join us

**Labcorp Medical Device & Diagnostic are expanding in EMEA.**

Medical Device trials are special, and we have a dedicated global team of 160+ experts, with 30 + years of device experience and 500+ studies in the last 5 years alone.

Now, we are strengthening our team in Europe and are actively looking for several Project Coordinators.

**Join a growing team that will catapult your career.**
- ** Previous extensive experience with Devices is not required**. We have distilled our Device expertise into one of the more robust training and mentoring programs you can find in the CRO landscape.
- **Nurturing talent from within is in Labcorp´s DNA**. Career progression is clear: we´ll train you today with the intention to develop you into a future leader in roles such as:

- Clinical Team Lead
- Line manager
- Global Project manager

**Who you are**

These are remote jobs and most based in any country in Europe.
- We need you to bring a **Life Science University/College Degree**, or certification in a related allied health profession (e.g., nursing, medical or laboratory technology). This is a **must**.
- You have **2-3 year’s relevant clinical research experience** at a CRO or pharmaceutical company as **In-house CRA**, **CRA** or **SSU Specialist**; or **Study Coordinator** in a hospital environment.
- Basic understanding of the clinical trials process **is a must**.
- Knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
- Computer competency with various programs (e.g., Microsoft Word, Excel, Project, Access and Power Point)
- Fluent English and local language, ability to communicate verbally and in writing

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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