Clinical Trial Coordinator
Il y a 3 mois
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
Clinical Trial Coordinator (Client dedicated) - Belgium, 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**:
- Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
- Reviews regulatory documents for proper content
- Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
- Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
- Assists with the identification of potential investigators and development/distribution of initial protocol packets
- Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes
- Providing administrative support for the submission team
**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
**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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