Intel Corporation is hiring a
Associate Director, Portfolio Management and Processes

Summary

The job is for an Associate Director of Portfolio Management and Processes at Immunovant, a clinical-stage immunology company. The role involves driving trial delivery, collaborating with various teams, defining strategy, identifying and mitigating potential issues, and ensuring timeline compliance. The position is remote and requires some travel.

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

Responsibilities

• Collaborate with Sponsor and CRO Study Teams/sub-teams, local SRMs and local MSLs to drive trial delivery to plan
• Coordinate and ensure Site Management’s responsibilities between Study Teams and SRMs (feasibility, site selection, site activation, enrolment, site/trial closure, issue escalation, site visit planning)
• Ensure sufficient training in trial protocol/processes for SRMs
• Assist the clinical indication teams in the creation of clinical plans and trial feasibility by facilitating efforts to incorporate regional/local needs as needed
• Monitor and track trial level delivery of enrollment and milestones per trial level plans set by the clinical indication team and communication of results
• Facilitate Site Management and cross functional process development and implementation to enable delivery of portfolio; create library and mechanisms for sharing best practices
• Build collaborative relationships with key internal stakeholders to facilitate the planning, and execution of clinical trials, operational strategy, risk management and mitigation
• Provide input to trial level risks captured by the clinical indication team, report any new risks detected and support mitigations as needed across regions
• Serve as escalation point for clinical teams that have issues with clinical trial site-based deliverables

Preferred Qualifications

Experience in rare disease therapeutic areas and patient engagement strategies preferred

Benefits

• Compensation is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Equity, sign-on bonuses, and other forms of compensation may be provided as part of a total compensation package
• In addition to a full range of medical, dental, vision, 401k and other benefits, including unlimited paid time off and parental leave
• The annual base salary for this position ranges from $170,000.00 - $185,000.00
• Domestic or international travel are required (10-20%)