Clinical Director

Responsibilities:

Manage and execute pre-clinical and clinical studies activities in Israel and the US.

Accountable for clinical project management; from clinical strategic, and protocol development to final reports and publication (i.e. including study documentation, site selection, enrollment, follow-up, monitoring, data analyses, and reporting)

Lead resources to ensure the successful execution of clinical studies. Directly visit and own clinical sites as part of global studies

Management of local Research Administrators (CRA) to ensure project monitoring.

Develop reports for submission to regulatory agencies and internal/external publications.

Qualifications:

Graduate qualification in Life Sciences, medicine, or medical sciences.

At least 10 years of Experience in managing clinical studies from Initiation to FDA submissions.

Experience with defining clinical and pre-clinical studies according to development and regulatory needs.

Experience with clinical trials of a therapeutic product (a diagnostic product will not suffice)

Experience in working with Israel MOH, CRO’s

Hands-on experience in preparing clinical documentation.

Experience in working in a team setting in a collaborative manner.

Fluent English

Location: Nesher