Associate Director, Portfolio Management and Processes

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Immunovant

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Dedicated to enabling normal lives for people with autoimmune diseases

Biotechnology Research

51 - 200

Description

•Organizational Overview: •Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. •The Role: •Responsible for driving and collaborating with Sponsor Team, CRO, and SRM. •Partner with groups to define strategy to achieve trial-specific corporate targets. •Identify and mitigate potential issues and ensure timeline compliance. •Collaborate with Sponsor and CRO Study Teams/sub-teams. •Coordinate responsibilities between Study Teams and SRMs. •Ensure sufficient training in trial protocol/processes for SRMs. •Assist clinical teams in creation of clinical plans and trial feasibility. •Monitor and track trial delivery of enrollment and milestones. •Facilitate cross functional process development and implementation. •Build collaborative relationships with key internal stakeholders. •Provide input to trial level risks and support mitigations as needed. •Serve as escalation point for clinical teams with site-based deliverables.

Requirements

•Bachelors in Life Sciences with an advanced degree preferred •At least 8 years of experience in the pharmaceutical industry, with at least 5 years in a clinical role on a cross-functional drug development project team •Global experience working across all phases of clinical research (Phases 1-4) •Demonstrated ability to manage cross functional teams and diverse set of stakeholders •Multi-tasking ability to oversee many projects and reach milestones on time •Strong project management skills with proven track record of success using project management tools •Working knowledge of ICH and GCP regulations is required •Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems or equivalent. •Understanding of clinical trial operations and management of clinical trials at investigator sites •Experience in rare disease therapeutic areas and patient engagement strategies preferred •Unrelenting dedication to delivering quality results •Influencing without authority •Willingness to roll up your sleeves and get in the weeds of projects as a jack of all trades •Ability to think outside of the box and challenge the status quo •Natural entrepreneurial spirit with unrelenting dedication to delivering results •Natural collaborator who enjoys working on a cross-functional team

Benefits

•Unlimited paid time off •Parental leave •Medical, dental, vision, 401k and other benefits •Equity and other forms of compensation