Career /Clinical Research Manager / Oncology

(H / F) Type of Contract : CDI _ Strasbourg Area

Minimum 5 years experience

Graduate (e) medicine (PhD) , you have proven experience of conducting clinical trials in oncology, in an international context.

You practice fluent English.

You enjoy teamwork and information sharing. Your fluid communication allows you to be able to put you to everyone. You have demonstrated your ability to synthesize under complex projects.
Missions

You have the opportunity to support the launch of our studies of innovative immunotherapeutic products in combination with "checkpoint inhibitors" in the field of oncology.

In this context, you have the responsibility to implement the clinical development plans for a range of products as well as international clinical studies that result.

You bring your medical expertise in the conduct of these studies. You integrate a human dimension to team invested on ambitious targets.
Your main tasks are:

• Coordinate and plan the clinical development of products: you define the clinical development plan of a product as part of its development plan strategic.
• You propose the design of clinical study protocols and validate. You make the production of clinical trial protocols and consent forms.
• To be player in communication between stakeholders of a clinical project: You organize and animate up meetings clinical studies with various internal stakeholders and external .
• You present and discuss the clinical development projects with health authorities, opinion leaders and with pharmaceutical partners.
• You identify the opinion leaders in the field of therapeutic area studied.
• Analyze and interpret results of clinical studies: you ensure the monitoring and analysis of clinical trial data being that the benefit-risk patients in clinical studies is preserved and that the conduct of the clinical trial is consistent with expected from the research.
• You participate in data analysis and make the medical validation of data resulting from clinical studies.

Finally, make sure the writing and validation reports and publications of the results of clinical studies.

- To ensure and improve the quality of clinical studies: you are responsible for the quality of clinical activities on the project and in particular the quality of data.

Mickael Bauman

Market Researcher
NonStop Pharma

Tel: 00 33 176 753 340 | Int Ext: 3175
Email: m.bauman@nonstop-pharma.ch
Web: www.nonstop-pharma.ch
NonStop Recruitment Schweiz AG | Baarerstrasse 135 | Zug 6300 | Switzerland