Clinical Scientist Biotech (PR-33781684)

Ort: München, Bayern, Deutschland
Gehalt: Vergütung aller Überstunden
Spezialisierungen: Life Sciences
Vertragsart: Festanstellung
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Sie haben Erfahrungen im Bereich der Clinical Development und suchen den Sprung in die Biotechnologiebranche? Dann sind Sie genau der/ die Richtige für folgende Position, die ich im Augenblick betreue:

Clinical Scientist

Responsibilities:

Responsible for providing medical / scientific input and expertise to individual clinical trial(s) within a global development program of a disease area

For the assigned clinical trial(s) within program, as a member of the CTT, provide medical scientific input to: all activities related to planning, execution and reporting of clinical trials; development of trial related documents (e. g. protocols, case report forms, data analysis plan, reports, publications); development of presentation material for trial-related advisory boards, investigators meetings, protocol training meetings for CRO

Ongoing review of clinical trial data, final analysis and interpretation, in collaboration with the Safety Leader and appropriate CTT members.

Build relationships among the clinical/scientific community and with external experts

Represent Clinical Development in Clinical Trial Teams, participate and contribute in clinical subteams and other committees needing medical support

Maintain sponsor oversight on data quality and product safety in clinical trials via regular medical monitoring activities in collaboration with the Safety Leader and appropriate Clinical Trial Team members. Perform hands on medical data review, as needed.

Support regulatory authority interactions, information requests etc (e.g. FDA and EMA) As needed, and based on individual expertise, perform evaluations of potential drug targets and drug candidates for future clinical development

Requirements:

Ideally PhD or PharmD in health sciences / translational research with substantial experience in clinical development

Strong background in haemato-oncology, oncology or immuno-oncology

Experience in early or late drug development

Ideally minimum five years of relevant professional experience with at least two years in the pharmaceutical or biotechnology industry

Prior experience in regulatory authority interactions / submissions preferred but not a must

Haben Sie Interesse an dieser Position? Dann freue ich mich auf Ihre Bewerbung und ein interessantes Gespräch mit Ihnen.


Herzliche Grüße,

Stefan Blöchl

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