Protagonist Therapeutics, Inc.

Associate Director/Director, Program Management

Protagonist Therapeutics, Inc.$175K — $225K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific or business discipline required; 10+ years of Program Management in biopharma desirable.
  • PMPP certification is a plus for candidates.
  • Proficient in Microsoft Project, Smart Sheet, PowerPoint, and Excel.
  • Experience in a fast-paced, entrepreneurial development environment highly preferred.
  • In-depth knowledge of global drug development processes essential.
  • Experience across multiple therapeutic areas is advantageous.
  • Strong organizational, presentation, and facilitation skills required.

Responsibilities

  • Create and manage project timelines using planning tools like Smartsheet and Gantt charts.
  • Conduct project team meetings and provide concise minutes with key decisions and actions.
  • Drive Ph1 and Ph2 program timelines with clinical leads to optimize resources and risk.
  • Ensure project planning aligns with agreed time, resources, and budget.
  • Document project activities while identifying issues, risks, and leading contingency planning.
  • Facilitate conflict resolution within project teams.
  • Present strategic project updates and options to senior management.

Benefits

  • 100% premium coverage for medical, dental, and vision for employees and dependents.
  • Flexible Spending Accounts for healthcare, dependent care, and commuter benefits.
  • 401(k) Retirement Plan available.
  • Flexible Vacation Policy promotes work-life balance.
  • Life Insurance options including basic, voluntary, and AD&D.
  • Short-term and long-term disability coverage included.
  • Complimentary lunch and snacks provided on-site.
Full Job Description
Associate Director/Director, Program Management

Position Summary

The Associate Director/Director, Program Management is a critical function and will be responsible for leading and coordinating all activities associated with advancing a program through Ph1 to Ph3 clinical trials. The individual will be a key member of project teams, working closely with the stakeholders and contribute to the definition of project strategy and guide the project and functional teams to deliver on program and corporate objectives. This position will be accountable for steering core teams through internal processes and manage the integration of preclinical, clinical, cmc, and regulatory execution. Develop and ensure timely execution of complex project plans, as well as manage project timelines, budget to achieve key milestones and timely decision points.

We are committed to a thriving in-office culture. This role requires being on-site at our office in Newark, CA 4 days a week.

Responsibilities
  • Create timelines and utilize planning tools such as creation of project dashboards and Gantt charts including Smartsheet. Ensure team objectives are clearly established and communicated. Ensure that responsibilities are understood, risks are identified, progress is measured and plans are updated and adapted as necessary.
  • Organize and conduct project team meetings. Provide concise meeting minutes in a timely fashion, including key decisions and actions.
  • Work with respective functional leaders to drive the Ph1 and Ph2 programs including clinical timelines in collaboration with the clinical lead that optimize value, time, resources and risk while ensuring that Program strategy is aligned with business objectives.
  • Accountability for ensuring adherence of project planning and activities to agreed time, resources, budget and scope.
  • Accountability for project team documentation and for identifying issues and risks and leading contingency planning. Identify and track the project's critical path, formulate and monitor corrective courses of action
  • Ensures conflict resolution at project team or higher level.
  • Presenting strategic issues, project updates and options, and recommendations to Senior Management team.

Required Skills & Qualifications
  • Minimum Bachelor's degree in a relevant scientific or business discipline and 10+ years of relevant Program Management / Project Leadership in the biopharmaceutical industry or equivalent. PMPP certification a plus.
  • Strong organizational, facilitation and presentation skills
  • Advanced Microsoft Project, Smart Sheet, PowerPoint, Excel capabilities
  • Prior experience working in a fast-paced entrepreneurial development stage company is highly desirable.
  • In depth knowledge and experience of the global drug development to enable robust and efficient project plans
  • Experience in more than one therapeutic area would be a plus.
  • An ability to take hands-on, "roll up your sleeves" approach toward achieving business results.
  • An ability to achieve results with colleagues of diverse functional expertise, skills and priorities. This would include the ability to challenge the status quo where relevant, and resolve conflict within the team while maintaining clear focus on business objectives. It also requires the ability to lead by influence rather than by command.
  • Highly motivated, proactive and organized with an ability to operate independently
  • Excellent interpersonal skills with an ability to develop collaborative relationships internally and externally
  • Excellent communication and analytical skills, with an ability to navigate, synthesize and convey complex issues
  • Financial acumen to develop and provide oversight of project budgets and product valuations, with an understanding of portfolio management concepts
  • Ability to translate strategy into action, requiring strong influencing, negotiation, and presentation skills
  • Ability to travel, about 5%

Pay Range

The base pay range for this position at commencement of employment is expected to be between $175,000 and $225,000/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

Benefits

A top priority for Protagonist Therapeutics, Inc. is to provide a robust and comprehensive health and wellness program for our employees and their families. We offer a variety of high-quality coverage and benefit options.
  • Health Care benefits. Protagonist covers 100% of the premium cost for medical, dental, and vision coverage for all full-time employees and their dependents.
  • Flexible Spending Accounts - Healthcare FSA, Dependent Care FSA, Commuter Benefits
  • 401(k) Plan
  • Flexible Vacation Policy
  • Life Insurance (Basic, Voluntary & AD&D)
  • Short Term & Long Term Disability
  • Company paid lunch and snacks

About Protagonist Therapeutics, Inc.

Protagonist Therapeutics, Inc. is a clinical-stage biopharmaceutical company that discovers and develops peptide-based therapeutics to address significant unmet medical needs. The company's pipeline includes PTG-300, an injectable hepcidin mimetic for the treatment of iron overload-related rare diseases, including beta-thalassemia and polycythemia vera; and PN-943, an oral, gut-restricted alpha-4-beta-7 integrin antagonist peptide for the treatment of inflammatory bowel disease. Protagonist Therapeutics, Inc. was founded in 2006 and is headquartered in Newark, California.
Learn more about Protagonist Therapeutics, Inc.
Size
122 employees
Market Cap
$483 million
Industry
Net Income
-$66.1 million
Founded
2001
Revenue
$28.6 million
NASDAQ

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