Associate Director of Clinical Trial Planning, Resource Management

Scorpion Therapeutics; United States; Remote; USD 165,000 - 215,000; Full time

Job summary

A leading biopharmaceutical company is seeking an Associate Director of Clinical Trial Planning to oversee clinical trial activities and resource management. This role requires extensive experience in pharmaceutical drug development and expertise in clinical trial planning tools. Join a pioneering team dedicated to advancing cancer therapies and make a significant impact in the field.

Benefits

Discretionary annual bonus

Stock-based long-term incentives

Paid time off

Medical, dental, vision, and life insurance plans

Qualifications

• 10+ years’ experience in pharmaceutical drug development.
• 8+ years’ experience in clinical trial plan management.
• Strong analytical and problem-solving skills.

Responsibilities

• Create and maintain detailed clinical trial project timelines.
• Coordinate resource inputs for departmental planning.
• Monitor data quality within Kite systems.

Skills

Analytical skills

Problem-solving skills

Interpersonal skills

Leadership skills

Education

BS/BA in nursing, science or health related field

MS/MA in nursing, science or health related field

Ph.D. in nursing, science or health related field

Tools

Planisware

MS Office Suite

Sharepoint

Tableau

Power Bi

Job description

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We’re here for one reason and one reason only – to cure cancer

Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

People Leadership

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

The Associate Director of Clinical Trial Planning, Resource Management, and Reporting is a member of the Portfolio, Project Management and Business Operations team within Development.

The role is accountable for clinical trial planning activities:

• Accuracy of the critical path timelines for multiple studies within a product and accurate representation of the development deliverables including clinical trial demand and strategic study milestone reporting.
• Facilitating scenario planning in Planisware to support decision making during portfolio prioritization and budget planning.
• Collaborating with cross-functional development project teams and organization.

Resource management and reporting activities:

• Maintaining accurate resource capacity and demand forecasting data in Planisware.
• Coordinating resource inputs for departmental planning and cross-functional project team meetings.
• Monitoring data quality within Kite systems, dashboards and reports used for portfolio planning and resource forecasting.

The position will report to the Director of Business Strategy & Operations.

Responsibilities include but are not limited to:

Clinical Trial Planning:

• Create and maintain detailed clinical trial project timelines, study startup schedules, and scenario-based planning models in Planisware.
• Partnering closely with Project Managers to ensure clinical trial plans have accurate information and milestones, deliverables, and dependencies are aligned across study teams.
• Maintain Kite’s planning environment.
  Ensure alignment of standardized project milestone activities across asset, product, and clinical plans.
  Update project templates and styles.

Resource Management & Reporting:

• Support Director of Business Strategy & Operations, extracting and analyzing resource data provided to Kite leadership and project teams.
• Review demand forecasts with cross-functional teams and project managers to gather accurate demand inputs.
• Ensure all data remains consistent and standardized for accurate reporting.
• Accountable for maintaining centralized Sharepoint sites, team mailboxes, and Planisware related training documents.
• Participate in user acceptance testing (UAT) for Planisware releases and provide training for current and new Planisware users.
• Act as the point of contact for planning and resource reporting tool related issues, updates, and enhancements.

Basic Qualifications:

• A BS/BA degree in nursing, science or health related field required with 10+ years’ experience in pharmaceutical drug development OR
• A MS/MA degree in nursing, science or health related field required with 8+ years’ experience in pharmaceutical drug development OR
• A Ph.D. degree in nursing, science or health related field required with 2+ years’ experience in pharmaceutical drug development OR

Preferred Qualifications:

• Highly experienced in clinical trial plan management and scenario planning using Planisware -8+ years of experience using Planisware for clinical trial planning and scenario planning, and 5+ years of experience in resource management and reporting.
• Cross-functional resource allocation and demand forecasting.
• Portfolio and resource capacity and demand reporting.
• Stakeholder communication.
• Risk assessment & mitigation.
• Utilization of project management core principles (PMP certification a plus).
• Deep knowledge of the end-to-end pharmaceutical R&D process, including preclinical through post-marketing. (Cell therapy/Oncology preferred).
• Capable of assessing and updating detailed project timelines in meetings to guide and align study team members.
• Adept at optimizing resource utilization, driving operational efficiencies, and aligning strategic priorities with project execution.
• Experience supporting cross-functional resource demand with the ability to consolidate, translate and provide resource analyses and portfolio data to leadership and project teams.
• Ability to prioritize and execute tasks both as an individual contributor and in a team-based setting.
• Strong analytical and problem-solving skills with the ability to multi-task, prioritize, and work on several complex projects while exercising critical thinking with minimal supervision.
• Excellent interpersonal, verbal, and written communication, and organizational skills are essential in this collaborative work environment.
• Demonstrates leadership skills, self-motivated, and comfortable in a fast-paced dynamic company environment with the ability to adjust workload based upon changing priorities.
• Strong computer skills, proficient using MS Office suite (outlook, word, excel, power point, teams), Sharepoint and other organization tools.
• Technical experience using Planisware, OnePager, Spotfire, Tableau, Power Bi and/or other business intelligence tools.

Compensation

The salary range for this position is: $165,495.00 - $214,170.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.

Additional Benefits Information

For additional benefits information, visit:

Gilead Careers - Compensation and Benefits

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

Company Overview

Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter.

Equal Employment Opportunity

For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [e-mail] for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT

YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.