Clinical Trial Coordinator

2 maanden geleden

Ede, Nederland Thermo Fisher Scientific Voltijd

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

Clinical Trial Coordinator (Client dedicated) - Hybrid

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

**Location/Division Specific Information**

PPD's Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.

Discover Impactful Work:
Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.

A day in the Life:

- Provides administrative support for the clients’ regulatory & ethics submission team
- Reviews regulatory documents for proper content
- Disseminates study related information, including project tracking updates to clinical study teams
- Assists with the preparation of documents and development/distribution of initial protocol packets
- Works in collaboration with team members to achieve targeted deadlines for EU-CTR submissions

Keys to Success:
**Education**
- University degree, or equivalent in education, training and experience

**Experience**
- Experience of managing multiple projects with differing priorities at one given time

**Knowledge, Skills, Abilities**
- Responsible for adhering to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout
- Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
- Exceptional communication, collaboration, organisational and time management skills.
- Fluency in English, French and Dutch languages
- Knowledgeable of IT systems and tools used

**Benefits**:
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation

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