Director/Senior Director of Project Management - South San Francisco, CA | Biospace
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Director/Senior Director of Project Management

Calithera Biosciences, Inc.

Location:
South San Francisco, CA
Posted Date:
6/8/2017
Position Type:
Full time
Job Code:
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:

Job Description

The Director will manage multiple projects at Calithera within the constraints of scope, quality, time and cost, to deliver specified requirements. The position will manage the initiation, planning, execution, control and close out of cross-functional projects and ensure integration, coordination, timing and consistency of processes throughout multiple projects, as well as manage the integration between CMC (manufacturing and supply chain logistics), clinical (trial preparation and execution) and preclinical (IND-enabling and supporting activities).

Duties and Responsibilities:
- Assemble comprehensive Gantt charts including specific resource allocation (person(s) responsible) for all preclinical- and clinical-stage programs integrating cross-functional activities to validate the project plans.
- Take a lead role in the development of a comprehensive Product Development Plan to support NDA filing and launch of a clinical program
- Provide and manage regular program-wide dashboards for each development program to Senior Management team.
- Review Gantt charts (or derivative PowerPoint charts) with team members on a regular basis to update, provide reminders, identify critical path items, develop action plans to solve critical issues, and elevate specific concerns to senior management.
- Guide and support team leaders in prioritizing, trouble-shooting and contingency planning.
- Evaluate timeline project overlap by providing cross-functional, cross-project Gantt analysis.
- Identify program-related risks and work with teams to develop mitigation plans.
- Manage program-wide communication of critical issues; provide formal and informal briefings on project status to team members, functional heads and senior management.
- Support the management of logistics in clinical operations activities by assembly and regular review of timelines for recruitment, drug pharmacokinetic and biomarker CRO activities, and study activation, conduct, and closeout.
- Work with clinical teams, CMC subteams and other contributors to identify critical issues, critical path, and project overlap.
- Working with Project Leaders, manage the preparation of program-wide development plans including full nonclinical, manufacturing, clinical development, regulatory, and quality management directed toward regulatory approval.
- Attend and record all project team meetings including critical issues, actions and responsibilities.
- Work with the team to develop project-related budgets.
- Manage all operational aspects of corporate partnerships.

Requirements

- BS or equivalent with at least 10 years experience in project management roles.
- Prior supervisory experience.
- Thorough knowledge of the role and function of project management in high-performing team environment.
- Direct experience with project management related to NDA filing is a strong plus.