Clinical Study Management

vor 2 Monaten

Hamburg, Deutschland Perfood Vollzeit

**Immediate Hiring**

We are looking for team members who are eager to help us reshape the future of nutritional medicine by combining personalized nutrition with digital medicine and thus help patients. We’re in search of reinforcement in the field of Clinical Study Management to actively participate and support us shape the development and research of innovative therapeutic.

**Skills and Requirements**:

- Completed university studies.
- Three (3) years of professional experience (outside a doctorate) with clinical and non-clinical studies.
- Experience in non-university industrial research, for example from Pharma, MedTech, or a CRO.
- Experience with metabolic diseases around metabolic syndrome and inflammatory diseases is an advantage.
- An understanding of (business) economic conditions and the effects of R&D investments on business development is an advantage.
- Solid knowledge of statistical study planning and evaluation.
- Willingness to assume personal responsibility.
- Very good knowledge of spoken and written German and English.
- Good PC skills, especially in dealing with MS Office programs.
- Very good organizational skills, independent and structured way of working, and decision-making skills.
- Empathy, motivation, flexibility, initiative, independence, communication skills, reliability, and enjoyment of working in a team.

**Tasks and Responsibilities**:

- Independent assumption of key tasks in close coordination with the Chief Medical.
- Officer and the management.
- Ensuring the successful study planning, implementation, and completion of the proof-of-concept, pilot, and approval studies of our software and medical products.
- Supervising/monitoring of studies and compliance with planning requirements, regulatory and ethical requirements (e.g. MDR, ICH/GCP), and quality objectives throughout the study.
- Selection, coordination, and monitoring of qualified study centers, external service providers (e.g. CROs) for study implementation, and other stakeholders such as ethics committees and regulatory authorities

**What's waiting for you**:

- A highly innovative and effective product in a fast-growing industry.
- A good and collegial team that will support you during your induction.
- The opportunity to significantly improve medical care for numerous diseases.
- Working together in an interdisciplinary team from the fields of medicine, nutritional science, data analytics, and artificial intelligence as well as law and business administration, and the associated opportunity to expand your existing knowledge beyond your own area of responsibility.
- The opportunity to actively support the establishment of a company with a highly innovative product in a fast-growing market.
- Snacks and drinks are freely available in the office.
- Beautiful office building in an old brewery with a view of the 7 towers of Lübeck.
- Choice of your work material.
- The position can also be filled remotely.

Art der Stelle: Vollzeit

Arbeitszeiten:

- Keine Wochenenden

Bewerbungsfrage(n):

- Do you have experience in non-university industrial research, for example from Pharma, MedTech or a CRO?
- Do you have experience in supervising/monitoring of studies and compliance with planning requirements, regulatory and ethical requirements (e.g. MDR, ICH/GCP)?

Ausbildung:

- Promotion/Doktorat (Wünschenswert)

Sprache:

- Deutsch (Erforderlich)

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