Clinical Trial Assistant
.jpg)
Salvia BioElectronics is a medical device company pioneering neuromodulation therapies for migraine. Salvia's unique, paper-thin implant is designed to reduce the frequency and intensity of migraine attacks by delivering gentle electrical pulses to the nerves associated with the condition. The company is currently in the clinical stage of development. In addition, Salvia is considering potential opportunities the device creates for the treatment of cluster headache and other neurological disorders. Salvia has received the Breakthrough Device Designation from the United States Food and Drug Administration (FDA), which facilitates expedited market access for devices that treat life-threatening or irreversibly debilitating conditions.
Salvia is a fast-growing and dynamic company; we are driven to make a difference for people living with severe migraine. With a focus on ongoing development, we are currently looking for a Clinical Trial Assistant. You will be part of the clinical team and able to work on clinical studies at various stages. The CTA is responsible for operational and administrative support throughout a clinical study. You work with great attention to detail; you embrace organization and dedication, and you have a passion for clinical research.
- Providing administrative support to Clinical Affairs;
- Providing administrative support to Medical Affairs and the Chief Medical Officer;
- Collecting, registering, and archiving information and documents per the applicable good clinical practice guidelines for clinical studies;
- Preparing investigator site files, trial master files (TMF), and, if applicable, electronic trial master files (TMF) for the initiation of participating centers in clinical studies;
- Maintaining the complete documentation for the studies assigned and ensuring all study documentation is up to date;
- Performing periodic review of study files for completeness;
- Assisting with preparation, handling, and distribution of clinical trial supplies and maintenance of shipping information;
- Supporting regulatory submissions and site start-up;
- Acting as a central contact for the Clinical Affairs team for designated project communications, correspondence, and associated documentation.
- Assisting in submissions of the study to regulatory authorities and ethics committees.
- May support CRA to perform clinical data review query creation and query resolution upon completion of required training.
- Minimum 2 years of experience in a comparable role;
- Accurate, eye for detail, independent and pro-active attitude;
- Excellent communication skills, able to collaborate and build relationships with people across all levels;
- Fluent in English;
- Knowledge of Good Clinical Practice (ICH, ISO 14155), Data Protection(GDPR) and Clinical Research laws and regulations
Page Title (H1)
Header (H2)
A subheading or chapter heading (H3)
Introductory text or a first paragraph of information on this subject. Write as naturally as possible and be nice and specific. If necessary, use AI software to help you get started, but definitely don't use it one-on-one. Search engines can penalize AI content.
Subheading (H4)
Here too there is more than enough room for a good story, an interesting article or background information. If necessary, use a summary:
- a summary is clear
- one can see the benefits or features at a glance
- also use search terms if necessary
Another topic (H3)
Another subheading (H4)
Do not use a Title Header (H1), but use an H2 Header instead. An H1 is actually a title of the page and may only appear once on a web page. The H2 is a kind of chapter and the other headers (H3 to H6) are subheadings and subheadings within the chapter. The order is important for the readability of visitors and search engines.
- a summary is clear
- one can see the benefits or features at a glance
- also use search terms if necessary
This way everything remains easy to read and understandable for the reader. People can also scroll directly to the topic they are interested in.
Paragraph heading style (H5)
This is another example of a heading. The headings H5 and H6 are usually used as paragraph headings, each with their own style.
Paragraph heading style (H6)
In the editor you can really see a difference in font size of all headers, but on the live website they have their own style.
Other options
Use a "quote". That looks like this:
This is a quote!
You can also put texts in bold, italic, etc.
Of maak een link naar een andere pagina of website.
And finally, you can also create Superscript(1) and Subscript(2) text.
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse varius enim in eros elementum tristique. Duis cursus, mi quis viverra ornare, eros dolor interdum nulla, ut commodo diam libero vitae erat. Aenean faucibus nibh et justo cursus id rutrum lorem imperdiet. Nunc ut sem vitae risus tristique posuere.
- Opsomming List Item
- Opsomming List Item
- Opsomming List Item
- Opsomming List Item
- Opsomming List Item
- Opsomming List Item
Block Quote
Will you be our new colleague?
Our team is growing and we are always looking for passionate and talented individuals who want to be part of our mission to give people with migraine a better life.
We encourage open applications. Please submit yours here!
Acquisition is not appreciated.
Other interesting jobs...
.jpg)
Equipment Engineer
We offer a challenging position for an accurate and disciplined Equipment Engineer. You will join Salvia’s operations team where your key responsibility is to develop and maintain production and verification equipment.
.jpg)
Operator
We offer a challenging position for an accurate and disciplined Operator. You will join Salvia’s production team where your key responsibility will be to consistently manufacture an implantable medical device. All production activities are conducted in a class 7 cleanroom.
.jpg)
Clinical Research Associate
With a focus on ongoing development, we are currently looking for a Clinical Research Associate. You will be part of the clinical team and able to work on clinical studies at various stages. The CRA plays a crucial role in ensuring the successful conduct of clinical trials by maintaining high standards of quality, compliance, and patient safety.