Director, Program Management

ADP, Inc.

San Diego (CA)

On-site

USD 200,000 - 220,000

Full time

4 days ago
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Job summary

ADARx Pharmaceuticals, Inc. in San Diego is seeking a Director, Program Management to oversee clinical asset development activities across functions, ensuring alignment with strategy, timelines, and budget.

The role leads cross-functional teams, partners with leadership, drives governance, manages risks, and champions best practices in program management for late-stage and regulatory submissions.

Qualifications

  • MS or PhD in Biology, Chemistry, Pharmaceutical Sciences, or related field.
  • 8+ years of project/program management experience in the pharmaceutical industry.
  • Experience with regulatory expectations and ICH guidance.
  • Proven track record building PM tools and templates and improving systems.
  • Experience leading programs from early development to late-stage milestones, including regulatory submissions.
  • Excellent written/verbal communication and presentation skills for senior management.

Responsibilities

  • Oversee across functions the successful execution of clinical asset development activities.
  • Lead cross-functional teams including Clinical Development, Clinical Operations, CMC, Nonclinical, Regulatory, and Bioanalysis.
  • Serve as a liaison between program teams and executive leadership; deliver updates and strategic recommendations.
  • Establish and enforce best practices in program management and governance.
  • Forecast capacity and manage timelines, risks, and dependencies; mitigate issues proactively.
  • Prepare research reports and presentations for internal and external audiences.

Skills

Program management
Cross-functional leadership
Regulatory knowledge
Project management tools
Communication skills

Education

MS or PhD in Biology/Chemistry/Pharmaceutical Sciences

Tools

Smartsheet
MS Project

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Director, Program Management

Full Time Director San Diego, CA, San Diego, CA, US

4 days ago Requisition ID: 1120

Salary Range: $200,000.00 To $220,000.00 Annually

Company Overview:

ADARx Pharmaceuticals, Inc., (the "Company" or "ADARx") located in San Diego, is a clinical stage biotechnology company dedicated to transforming cutting-edge science into next-generation RNA therapeutics to treat a broad spectrum of diseases. Our goal is to control the expression of specific disease drivers with highly selective RNA targeted therapies, delivering life-changing treatments for patients with urgent unmet medical needs.

Job Description:

The Director, Program Management’s primary responsibility will be to oversee across all functions, the successful execution of clinical asset development activities. This is a highly visible leadership position within the organization which requires ensuring and enabling alignment with corporate strategic goals, timelines, and budget constraints.

  • Develop and promote a workplace culture that values diversity of thought, promote integrity and create an atmosphere that supports coaching and fosters accountability.
  • Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner.
  • Establish and maintain excellent working relationships with critical collaborative partners throughout the company.
  • Partnered with an MD, lead one or more cross-functional clinical candidate development program teams comprised of representatives from Clinical Development, Clinical Operations, CMC, Nonclinical, Regulatory, and Bioanalysis.
  • Serve as a key liaison between program teams and executive leadership, delivering critical updates, strategic recommendations, and facilitating governance interactions.
  • Establish, maintain and enforce best practices in program management, knowledge sharing, and operational excellence
  • Timely revenue management and forecasting; high level capacity forecasting to support incoming business planning.
  • Understand and manage cross-functional tasks and timeline dependencies, including critical path activities and resource constraints.
  • Proactively identify risks to successful program execution and develop/implement requisite risk mitigation strategies and tactics.
  • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience.
  • Maintain all appropriate corporate standards for facility safety and hazardous material management.
  • Other duties as assigned.

Essential Physical Characteristics:

Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis.

On-Site Protocol:

Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

Qualifications:

  • MS or PhD in Biology, Chemistry, Pharmaceutical Sciences, or related field of study.
  • Project management with 8+ years of relevant experience in the pharmaceutical industry.
  • Must be well-versed in the various stages of pharmaceutical development, with a special emphasis upon regulatory agency expectations as defined in ICH guidance documents.
  • Demonstrated experience in building project management tools/templates, improving project systems and implementing best practices.
  • Proven track record in managing programs from early development and through late-stage clinical milestones, including regulatory submissions.
  • Excellent organizational, written and verbal communication skills; and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role.
  • Proficient in the use of project management tools (e.g., Smartsheet or MS Project).

Required Key Attributes:

  • Must be able to work independently with supervision as needed.
  • Proficient at working well in cross-functional team settings
  • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism.
  • Self-motivated with excellent interpersonal, organizational and communication skills with the ability to take a hands-on approach to work effectively in a dynamic and collaborative, fast-paced environment.
  • Strong problem-solving skills and a proactive attitude towards exploring new approaches.
  • Exceptional understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders.

ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Disclosure Statement

  • The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
  • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
  • The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law.
  • Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses.
  • Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.
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