Clinical Research Coordinator
Il y a 2 mois
We are looking for a **clinical research coordinator** to join our **FibriCheck** team, improving the lives of +1.000.000 happy customers.
FibriCheck is a dynamic and fast-growing company in the digital health sector. **Our mission is to save lives by improving the outcome of cardiovascular diseases.**
How? By developing device agnostic arrhythmia detection and prevention capabilities that are accessible for everyone, everywhere. FibriCheck is a full medical device - certified in different geographies including Europe, Middle East, Australia and the United States. FibriCheck has been used today by over 900.000 people, is prescribed by over 2.000 physicians and has processed over 8 million PPG measurements.
What strongly connects our employees is **our culture**. **Our values**. They help us to stay true to who we are. On a personal level we are looking for a colleague who shares** our values**:
- **Team**: as a team, we celebrate our achievements and comfort each other during our failures. Your mindset needs to be team-oriented, and put the team first.
- **Diversity & inclusion **: we ensure that every voice is heard through collaboration and valuing different perspectives. We accept and respect people for who they are, and we don’t judge people who are different to us. We believe that it’s our differences that make us stronger and diverse thinking makes our decisions better. We know that only by collaborating as one team will we deliver a brilliant service to our customers.
- **Innovation**: we are not afraid of challenging the status quo to grow our business and ourselves as an individual and as a team.
**Responsibilities**:
- **Clinical Trial Management**: the process of planning, coordinating, and implementing a clinical trial with external centers and/or clinical research organisations. This includes overseeing all aspects of the trial from start to finish, including study start-up activities, monitoring the trial as it progresses, and managing the study close-out activities.
- **Study Documentation Support**:refers to the preparation, review, and monitoring of all study-related documents. This includes but is not limited to informed consent forms, study protocols, case report forms, and other study-specific documentation.
- **Study Data Support**: assist in the management of study data, including support for project reporting and (intermediate) data analysis.
- **Clinical Relations**: overseeing and maintaining relationships with clinical partners, such as hospitals, research organisations, and healthcare providers. This includes building and nurturing relationships to ensure smooth collaboration, communication, and coordination throughout the course of the current study and future studies. This relationship, with potential future opportunities in mind, should inspire external partners to push the boundaries of cardiac monitoring.
- **Study Team Support**: provide assistance and support to the study team, ensuring that all team members have the necessary resources and information to successfully carry out their tasks. This may include coordination of team meetings, distribution of study-related materials, and resolution of any issues that may arise during the course of the study.
- **Internal and External Knowledge Sharing**:providing training and education to both internal staff and external partners. This may involve creating and delivering educational materials, providing (on-site) training, and answering questions related to the study or medical condition to ensure that all stakeholders have a clear understanding of the study protocols and procedures, and that they are able to effectively carry out their responsibilities.
**Your profile**:
As a Clinical Research Coordinator, you will be a key player in the successful execution of clinical research studies. We are seeking a proactive and detail-oriented individual with a critical mind and a passion for driving positive change.
Key elements ranked according to priority:
- **Communication and Interpersonal Skills**:be an effective communicator with excellent interpersonal skills, capable of building relationships with internal and external stakeholders., you’re eager to learn and you dare to challenge the status quo with a critical mind.
- **Relevant Experience**:possess several years of experience in clinical research or a related field, with a focus on study coordination.
- **Project Management**:demonstrate strong organizational and project management skills, with the ability to prioritize tasks, meet deadlines, and take ownership of project outcomes.
- **Team Oriented**: possess a positive, proactive attitude and the ability to work collaboratively with others to achieve company objectives.
- **Adaptability**:demonstrate resilience and flexibility, with the ability to work effectively in a fast-paced and dynamic environment.
- **Regulatory Compliance**: have a thorough understanding of Good Clinical Practice (GCP) guidelines
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