Clinical Research, Project Manager (PIT, PHX or FWD)

Castle Biosciences•Phoenix, AZ

31d•Onsite

About The Position

Castle Biosciences Inc. is growing, and we are looking to hire a Clinical Research, Project Manager working from our Pittsburgh, PA office, Phoenix, AZ, or Friendswood, TX office locations, with a start date prior to January 1, 2026. 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.
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.

Responsibilities

Management of all aspects of Clinical Study Team activities for assigned project(s)
Assisting in protocol development, eCRF design, operational planning, and resource allocation
Achieving successful delivery of activities at the project level by meeting regulatory requirements and study objectives according to schedule, quality, scope, and budget constraints
Ensuring studies are conducted in compliance with protocol, ICH GCP, FDA guidelines, SOPs, and applicable local regulations
Leading, managing, and mentoring study team members, providing direct supervision to clinical research associates, assistants, and associate project managers through regular coaching and guidance
Collaborating closely with cross-functional department teams to direct the clinical research aspects of product development
Assisting in the development of protocols, eCRF design, and the creation of study resource documents, reports, and presentations
Identifying and tracking study metrics, providing consistent updates to stakeholders to support the successful execution of studies