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Project Manager (PIT, PHX or FWD)

Castle Biosciences

Phoenix, AZFull-timeSeen todaySeen in employer's feed today

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At a glance

Compensation
No compensation found
Location
Phoenix, AZ
Schedule
Full-time
Work Authorization
Not specified

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Job overview

Castle Biosciences is hiring a Clinical Research Project Manager to manage clinical study team activities and deliver assigned projects within regulatory, schedule, quality, scope, and budget constraints. The role includes protocol and eCRF development, operational planning, resource allocation, team leadership, and stakeholder updates. The position works from the Pittsburgh, Phoenix, or Friendswood office and requires travel that is typically 1–2 times per year but may reach 50%.

Skills & qualifications

RequiredNice to have

Skills

Clinical ResearchProject ManagementPeople ManagementProject Management TechniquesProject Management Tools

Qualifications

Bachelor's or Associate's in Science or Equivalent or Registered Nursing CertificationHealth SciencesClinical Research Project Management or Equivalent Relevant ExperienceClinical Research Experience1 Year Managing Direct Reports

Benefits

Paid Time Off
401(k) Match
Medical Insurance

Full job description

This job was posted by https://www.azjobconnection.gov : For more information, please see: https://www.azjobconnection.gov/jobs/7264095 Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! You won't find a work culture and benefits package like ours every day. Come join our team and a group of colleagues who love working at Castle! Learn more atwww.CastleBiosciences.com Castle Biosciences Inc.is growing, and we are looking to hire a Clinical Research, Project Managerworking from our Pittsburgh, PA office, Phoenix, AZ, or Friendswood, TX office locations,with a start date prior to January 1, 2026. Why Castle Biosciences? - Exceptional Benefits Package: - Excellent Annual Salary + Bonus Potential - 20 Accrued PTO Days Annually - 10 Paid Holidays - 401K with 100% Company Match up to 6% - 3 Health Care Plan Options + Company HSA Contribution - Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Project Manager This position will be responsible for the management of all aspects of Clinical Study Team activities for assigned project(s), including assisting in protocol development, eCRF design,operational planning, and resource allocation. The Project Manager is accountable for achieving successful delivery of activities at the project level by meeting regulatory requirements and study objectives according to schedule, quality, scope, and budget constraints. They will ensure studies are conducted in compliance with protocol, ICH GCP, FDA guidelines, SOPs, and applicable local regulations. The Project Manager will lead, manage, and mentor study team members, providing direct supervision to clinical research associates, assistants, and associate project managers through regular coaching and guidance. This role will collaborate closely with cross-functional department teams to direct the clinical research aspects of product development, while also assisting in the development of protocols, eCRF design, and the creation of study resource documents, reports, and presentations. In addition, the Project Manager will identify and track study metrics, providing consistent updates to stakeholders to support the successful execution of studies. REQUIREMENTS - Bachelor's or Associate's degree in science or equivalent (Health Sciences field preferred), or registered nursing certification. - Strong medical or clinical research background. - Clinical research project management or equivalent relevant experience required. - Knowledge of project management techniques and tools required. - Experience in clinical research required. - Proven experience in people management. Minimum of 1 year managing direct reports. TRAVEL/WORK ENVIRONMENT - Typical travel is 1-2 times per year, but may be up to 50% at times - Proof of COVID-19 vaccination will be required to access study sites, in accordance with site-specific guidelines and subject to any applicable exceptions as required by Federal, State, and Local laws. SCHEDULE - Monday-Friday, 40 hours/week, exempt positions, working from our Pittsburgh, PA office, Phoenix, AZ, or Friendswood, TX office locations. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete ourmobile-friendly application.We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be bothchallenging and rewarding. We behave withintegrityand treat our

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