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$37.5K

$95K

How much do aacr jobs pay per year?

As of Jun 1, 2026, the average yearly pay for aacr in the United States is $91,584.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $94,500.00 per year, depending on experience, location, and employer.

What is an AACR job?

An AACR job typically refers to a position with the American Association for Cancer Research (AACR), a professional organization dedicated to cancer research. Jobs within AACR can range from scientific research roles to administrative, communications, and event management positions. These roles support the organization's mission to prevent and cure cancer through research, education, and collaboration.

What are the key skills and qualifications needed to thrive in the Aacr position, and why are they important?

To thrive as an AACR (Association for the Advancement of Cost Engineering Certified Cost Reviewer), you need a solid background in cost engineering, project controls, and a relevant engineering or construction degree. Proficiency with tools such as Primavera, MS Project, and cost estimating software, as well as certification from AACE International, is highly valued. Strong analytical skills, attention to detail, and the ability to communicate complex data clearly with stakeholders are important soft skills. These competencies are essential for ensuring precise project cost management, minimizing budget risks, and supporting informed decision-making throughout large projects.

What are some common challenges faced by AACRs in their day-to-day work?

AACRs often handle the complex task of accurately reviewing and verifying project cost estimates, budgets, and forecasts, which requires meticulous attention to detail and strong analytical abilities. They may encounter challenges such as incomplete data, shifting project requirements, or balancing multiple projects with tight deadlines. Effective collaboration with project managers, engineers, and finance teams is also key to resolving discrepancies and ensuring cost accuracy. Overcoming these challenges helps to keep projects on track financially and supports transparent reporting to stakeholders.
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Aacr jobs near you

Scientific Program Manager, AACR Project GENIE

American Association for Cancer Research

Philadelphia, PA • On-site

Full-time

Posted 27 days ago

Job description

Overview
About the Project
AACR Project Genomics, Evidence, Neoplasia, Information, Exchange (GENIE) is an open-source, international, pancancer registry of real-world data assembled through data sharing between 18 of the leading cancer centers in the world. Through the efforts of strategic partners Sage Bionetworks and cBioPortal, the registry aggregates, harmonizes, and links clinical-grade, next-generation cancer genomic sequencing data with clinical outcomes obtained during routine medical practice from cancer patients treated at these institutions with the goal of improving clinical decision making and catalyzing clinical and translational research (www.aacr.org/genie).
Summary
The AACR Project GENIE Coordinating Center (GCC) is seeking a dynamic and highly organized scientist, clinical researcher, or epidemiologist with program or project management experience to lead and expand a portfolio of clinical research initiatives. This position will oversee both the implementation of new studies and the management of existing projects that leverage and enhance the GENIE infrastructure. The ideal candidate will bring a blend of scientific acumen and operational expertise, with demonstrated experience managing complex, multi-stakeholder projects. They will be comfortable engaging with diverse audiences -including technical experts, external collaborators, and senior leadership-while independently driving work forward in fast-paced, collaborative environments. The ideal candidate will also demonstrate a customer-facing mindset, attention to detail, and a proven track record of delivering high-quality outputs on time.
Responsibilities
  • Collaborates closely with the GCC Business Development team and external stakeholders to scope, plan, and deliver clinico-genomic research and infrastructure projects.
  • Partners with the GCC Project Management Office (PMO) to lead the organization, initiation, execution, and delivery of a portfolio of clinico-genomic and infrastructure projects.
  • Engages with data providers, strategic collaborators, project sponsors, and internal teams to facilitate the efficient identification, aggregation, and availability of datasets necessary to support new and existing projects.
  • Develops, maintains, and updates key project documentation (standard operating procedures, project plan, data guides, etc.), as necessary.
  • Supports the preparation and distribution of project-related communications to participants, strategic partners, and sponsors.
  • Contributes to the creation of external-facing communications and reporting related to project activities and milestones.
  • Performs other duties as assigned.

Job Tasks
  • Facilitates project scoping, organization, and execution through collaboration with internal teams and external partners.
  • Conducts project risk assessments and implements mitigation strategies to ensure timely and successful project delivery.
  • Participates in the development and maintenance of all project documentation (SOPs, project plan, data guides, etc.) as well as maintenance of the project website and related infrastructure.
  • Develops, manages, and executes project communication plans, ensuring clear coordination among stakeholders.
  • Uses project management platforms (e.g., Smartsheet) to track progress, assign tasks, and maintain timelines.
  • Develops agendas, meeting materials, and presentation decks; documents and distributes meeting minutes and action items.
  • Coordinates cross-functional input for the development of external project communications.
  • Conducts onboarding sessions and provides training for project team members.
  • Ensures compliance with data governance policies and creates or refines procedures in coordination with internal and external compliance officers.
  • Oversees project completion activities, including documentation archiving, final reporting, and capturing lessons learned.

Qualifications
  • PhD, MD, MS, or equivalent in a relevant field such as health informatics, epidemiology, population health, biomedical sciences, or a related discipline, with demonstrated knowledge of cancer genomics or molecular oncology.
  • Minimum of 3-5 years of experience managing complex, large-scale scientific or clinical projects involving multiple departments or institutions.
  • Excellent written and oral communication skills.
  • Strong organizational, administrative, and leadership skills.
  • Proven ability to engage and collaborate with diverse stakeholders, including scientific collaborators, industry sponsors, technical teams, and senior leadership.
  • Proactive, self-motivated, self-directed, and detail-oriented with strong critical thinking skills and a data-driven approach to problem-solving.
  • Demonstrated ability to manage multiple concurrent workflows while meeting deadlines.
  • Competence in using modern project management platforms (e.g., Smartsheet) to track and deliver outcomes.
  • Familiarity with MS Office and other standard software.

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