Clinical Site Manager Lead I

Clinical Site Manager Lead I

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians.  If you want to be part of this exciting work, you belong at Astellas!

Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at  www.astellas.com .

Purpose and Scope :

This position is accountable for the direct management of assigned late phase monitoring / site management related clinical trial staff across all clinical trial types, which may include post-POC interventional drug trials, pre-approval access and post-marketing regulatory commitment trials (interventional and non-interventional).

Accountable for the identification, onboarding, training and development of monitoring clinical trial talent to support the planning, initiation, execution and close-out of clinical trials with operational excellence.  Individuals in this role will also provide leadership / mentorship, in a matrix setting, for activities that support clinical trial teams.

This position is accountable to the Head, Late-Stage Site Monitoring & Management, and will provide input into departmental budget and resourcing strategies, including development and implementation of global processes and procedures, non-drug product initiatives, and coaching of monitoring staff during execution of development trials.

• This is a fully remote role that can be based anywhere in the US

Essential Job Responsibilities :

Quantitative Dimensions :

Responsible for overseeing, developing and aligning resources to ensure effective monitoring of clinical trials and a robust talent pool.