Clinical Study Consultant Generics (m/f)

REFERENZNUMMER:

237171/3

IHRE AUFGABEN:

-Ensure decision making for clinical studies, and organize respective communications internally, and/or with other companies (in a consortium), and/or with Health Authorities (Referral studies)
-Ensure studies are implemented and reported as required if studies are not conducted, ensure this is communicated to the relevant parties, internally to exit/prune the product (Referral studies)
-Ensure that adequate standards & procedures (e.g., GOPs, oversight tools, audits, training, etc.) are in place (Post-marketing)
-Ensure studies are conducted in full compliance with external and internal standards globally (Post-marketing)
-Ensure these standards are known and understood, and implemented, globally, and respective central oversight of any non-compliances exists, and is escalated and addressed as appropriate (Post-marketing)
-Implement a respective IT tool, as needed (Post-marketing)

IHRE QUALIFIKATIONEN:

-Profound experience in Pharmaceutical Industry, in Project Management and/or Study Management, ideally has designed / conducted studies
-Academic degree in life sciences (Physician, Pharmacist, or equivalent)
-Great communicator, outgoing personality, able to talk to Senior Mgmt. representatives
-Ability and desire to drive projects autonomously, while involving the right internal stakeholders & decision making bodies
-Attention to detail, and high quality and precision of documents / documentation
-Fluent in English (ideally native speaker)

WEITERE QUALIFIKATIONEN:

Clinical development manager