Clinical Scientist

 

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.

 

This position is based remotely in Canada.  Candidates interested in remote work are encouraged to apply.

 

Purpose and Scope:

The primary purpose of the Development Scientist will participate in the development of clinical strategies for assigned modalities or indications within the division. This position will work closely with the Global Medical Lead (GML), Operations Lead, and Asset Lead, and Medical Monitor, and is accountable for the design, implementation, monitoring, and analysis of clinical studies conducted within the assigned program. Development Scientists are expected to perform their responsibilities independently and have core knowledge of clinical development to enable increased participation in division and portfolio level initiatives.

 

Essential Job Responsibilities:

Responsible and accountable for activities related to all current and planned clinical trials (e.g., develop protocols, investigator brochures, CRFs, informed consents, and clinical study reports and review of clinical trial documents, study analyses, and reporting) on assigned development programs. Provides expertise to cross-functional team members to synthesize/contextualize data to facilitate discussion and timely decision making. Serves on the clinical sub-team with GML, Operations Lead, and Medical Monitor/Study Physician and supports preparation of clinical development plans, site identification and management, and DESC meetings. Under the guidance of study physician/med lead, perform medical monitoring activities (Review, analyze and triage patient data, generating reports Able to independently lead working groups and/or sub-team initiatives in support of protocol, disease area, or clinical development plan. Partners with GML in preparing for Health Authority (HA) Meetings and assists in addressing HA inquiries. Together with the GML and Product Responsible Person may prepare analysis for DMC/DSMB/DEC forums or regulatory submissions. Provides training at investigator meetings and site initiation visits with clinical trial staff, and partners with Clinical Operations and Medical Affairs in enabling appropriate enrollment into the clinical studies or registries. Collaborates cross-functionally to create, review, and/or present clinical slides for internal meetings and external forums. Supports engagement with potential and current sites (e.g. SIVs, investigator meetings, conferences, steering committee, advisory board meetings). Early and/or late phase studies Exhibits expertise related to Study Data Review and Analysis: Provides clinical input into statistical planning, data analysis and interpretation Provides clinical leadership and support for publication of data (manuscripts, presentations) and disease or technology related scientific publications Works closely with operations group for site and vendor feasibility, trial set up and monitoring. May lead the execution of contracts, particularly for investigator meetings and advisories. Supports efforts to develop strategic partnerships with Key External Experts (KEEs) Serve as key partner for Development Division in assessment of candidates within discovery, identifying opportunities and potential risks with future development strategies based on modality, indication, unmet need, competitive landscape and clinical characteristics. May represent development and assist with clinical assessment for due diligence(s) of new assets for potential in-licensing and acquisition. Supports strategic initiatives related to assigned molecule(s), CDP, therapeutic area(s), or portfolio, if requested. Performs other duties as assigned or special projects as needed.

 

Organizational Context:

This position reports to the Primary Focus Medical Head (or other Leads depending on grade) for designated program. This position is typically an individual contributor role, but may have direct reports based on scope, accountabilities and complexity of assigned development programs. If position has direct reports, will align with Astellas guidelines for span of control and organizational levels.