Clinical Scientist

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Beschreibung

Clinical Scientist - Biomedical / Oncology / MS Office / Data Analysis / English

Role:

For our pharma Roche Diagnostics in Rotkreuz we are looking for a Clinical Scientist (m/w/d).

Background:

We provide clinical expertise and leadership for the medical value innovation pipeline of novel diagnostic solutions across all relevant disease areas at RDS to achieve the Roche 10-year ambition. In close collaboration with many stakeholders, we also define the clinical product specifications, development strategies, and clinical study designs for product registration with adept medical writing, regulatory, and safety expertise.
Oncology & Genetics
We provide medical expertise supporting the development of innovative solutions for the diagnosis and management of cancer and genetic diseases
The perfect candidate:
The ideal candidate is someone with a Masters or Doctoral degree in a biomedical, public health, epidemiological or medical field, around 3+ years of experience in clinical research and is a good analytical thinker with an innovation mindset. On a soft skill note, the perfect candidate is able to be supportive, independent, with good communications skills & a team player. Please only submit candidates who are available immediately.

Areas of responsibility:

- The incumbent works proactively with CPS and global functions to analyze products of the CPS portfolio with regards to clinical evidence requirements according to the IVD[1]Regulations across all indication areas, and develops strategies to fill eventual evidence gaps.
- Work with Regulatory, Clinical Operations, Lifecycle teams, and R&D to generate Scientific Validity Assessments, Clinical Performance reports, and support the development of product requirements and specifications according to the IVD-Regulations (in vitro diagnostics).
- Support Global Clinical Leaders (GCL) and Clinical Science Leaders (CSL) in the assessment and definition of Intended Uses (IU) and clinical testing purposes of CPS products.
- Assess clinical evidence and state of the art in medicine related to the CPS products and IUs to demonstrate clinical benefit and safety.
- Document proof of training according to SOP 'Mitarbeiterentwicklung / Employee Development'
- Ensure continuous improvement of Medical and Scientific Affairs workflow to increase quality and efficiency
- Optimizes processes in order to increase quality and efficiency standards.

Must haves:

- Min. Masters degree in biomedical, public health, epidemiological or medical field
- Min. 3-5 years of experience clinical research, preferably in Oncology
- Good IT tools knowledge especially with MS Office and/or gSuite
- Good Data Analysis skills
- Willingness to learn, positive and open mindset, great team player
- Innovation mindset and spirit
- Excellent communication skills
- Fluency in English written and spoken is a must

Reference no: 921711SKN
Role: Clinical Scientist
Industry: Pharmaceutical industry
Workload: 100%
Location: Rotkreuz, Switzerland
Start date: 01.09.2022
Duration: 12 months contract, with possible extension

About us:

ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
Start
08/2022
Dauer
12++
(Verlängerung möglich)
Von
ITech Consult AG
Eingestellt
09.07.2022
Projekt-ID:
2421912
Vertragsart
Freiberuflich
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