Lead Clinical Research Associate (m/w/d), full-time

Andita Paramitha 9. December 2024

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phenox GmbH is a specialized manufacturer of Class III medical devices for the treatment of neurovascular diseases, which are developed, manufactured and distributed. Our innovative technologies and solutions are used by neuroradiologists worldwide to treat strokes and aneurysms. We offer a growing portfolio of innovative treatment options - including long-established technologies.

To enlarge our clinical programs team we are looking a s soon as possible for a

Lead Clinical Research Associate(m/w/d), full-time

Your job duties

Leading a team of assigned CRAs across different countries, you coordinate and guide their work to ensure study milestones are delivered efficiently, accurately, and on time
Actively participating in the creation of clinical monitoring plans, monitoring tools, visit report annotations, and CRA training materials, you also promote the ongoing enhancement of monitoring SOPs and templates to make monitoring activities more efficient and intelligent
With your experience and expertise, you train and mentor CRAs on study- and monitoring specific requirements, maintaining full training compliance and building a culture of excellence and accountability
Conducting co-monitoring visits internationally or, if necessary, on-site visits in the DACH region, including SQV, SIVs, IMVs or COVs, to guarantee consistency, quality, and strong relationships with our clinical sites throughout
Assisting each study in getting off to a good start and maintaining timelines by supervising regional start-up and feasibility activities
Working closely with clinical project managers, study coordinators, and data managers, you share insights, overcome challenges, and continuously drive best practices forward
You also ensure that CRAs always keep their sites inspection-ready, including maintaining a complete and compliant Investigator Site File and Trial Master File (TMF) for potential health authority inspections

your profile

A bachelor’s degree (or equivalent), ideally in life sciences, medicine, or a related field
At least five years of experience in clinical research within an international environment, including a minimum of three years in clinical site monitoring
Knowledge of relevant regulations such as ICH, GCP, ISO 14155 and GDPR
A passion for continuous learning, you enjoy developing your skills and staying up to date through regular training or on-the-job experience
Excellent communication skills in both writing and speaking, combined with strong interpersonal abilities and a talent for organization
A proactive mindset, you are detail- and solution-oriented as well as reliable
Willingness to travel within the DACH region and across Europe (up to 35–45% travel time)
Fluent in German and English; knowledge of any additional language is welcome
Previous experience in line management of CRAs would be a plus

We Offer

Be part of an international and dynamic team where collaboration and a hands-on mentality drive daily work
A flexible working environment that supports a healthy work-life balance e.g. this role can be on-site in our Bochum office, hybrid or remote
Benefit from a comprehensive onboarding program to help you quickly feel at home and succeed in your role
Grow with us - we offer the possibility to evolve within the team and take on new responsibilities
A fair and motivating remuneration system that values your contribution
Attractive benefits such as a company pension scheme (bAV) and capital-forming benefits (VWL)
Celebrate successes together at regular company and team events
JobRad as a sustainable alternative for your commute to work and in your free time

Does this appeal to you?

Then please send your complete documents, including the earliest possible starting date and your salary expectations, exclusively as a PDF file by e-mail to:

bewerbung@wallabyphenox.com

**Job Types:**Full Time

**Locations:**Remote - Europe

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Lead Clinical Research Associate*in (m/w/d)

Lead Clinical Research Associate*in (m/w/d)