Regulatory Coordinator

Overview

Join a Legacy of Care – Delivering over 50 years of Healing and Hope For over five decades Cancer Care Northwest has been the Inland Northwest's premier cancer center, providing an integrated approach to the diagnosis, treatment and healing of cancer and blood-related diseases. Our collective passion to fight against cancer is what motivates and inspires us every day and is the reason Cancer Care Northwest has become the Inland Northwest's premier cancer center.

We provide comprehensive, innovative, compassionate, integrated care throughout each patient's journey. We are searching for dedicated professionals who share our passion in saving lives. Are you searching for better work-life balance? Join us in our mission to save lives.

Position Overview

Under minimal supervision, is responsible for overseeing the regulatory management of industry or federally sponsored or investigator-initiated research studies. This includes the rules and regulations concerning Code of Federal Regulations, Good Clinical Practice and other regulations that govern clinical research studies.

This may include, preparing, facilitating, coordinating, and submitting documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research to the IRB central or local and IBC to assure the protection of human subjects in research for all CCNW trials. May assist with data completion and monitoring activities along with Quality assurance projects.

Supports and adheres to the Cancer Care Northwest Compliance Program, to include the Code of Ethics and Business Standards.

Responsibilities

Have knowledge and represent the research program in all regulatory affair requirements, interacting with local, state and federal agencies. Submissions of regulatory documents including but not limited to: initial IRB forms, 1572 forms, financial disclosures, annual reviews, amendments, investigational new drug applications, device related trial submissions, safety reports, and continuing reviews.

Track submissions and ensure timely filing of documents. Responsible for organizing and maintaining up to date clinical trial information, including study protocols and informed consent forms, for accurate presentation to physicians and study staff to ensure patient safety. Directly communicates with sponsors, study staff and Institutional Review Board Coordinators as it relates to study specific document modifications and Institutional Review Board requested revisions.

Tracking staff training to all applicable regulatory requirements including but not limited to GCP, Human subjects’ protection, hazmat ( IATA) training, and all study specific related training. Help to create/develop CCNW standard operating procedures to ensure staff understanding of required compliance and research participant safety.

Must be detail-oriented and be able to multi-task to meet standard response times and deadlines. Must be able to demonstrate appropriate conflict resolution in stressful situations. Demonstrate superior customer service skills. Demonstrate the ability to work independently and as part of a team. Any other duty as assigned.

Qualifications

Bachelor’s degree or equivalent combination of education and experience. Proficient with Microsoft Office It is preferred an individual has: Regulatory experience in clinical research Oncology experience Physical Demands: Regularly: stand, walk, grasp, reach, talk, and hear Occasionally : lift to 40 pounds, pull/push up to 40 pounds, carry up to 40 pounds, bend, and stoop/crouch Vision: clearly see up to 5 feet with or without corrective lenses Work Environment: While performing the essential duties/responsibilities of this job, the employee will: not be exposed to any workplace environmental conditions caused by extreme noise, heat, cold, workplace hazards, or atmospheric dust/fumes/vapors/mists be exposed to blood borne pathogens be exposed to toxic or caustic chemicals be exposed to ionizing radiation, medical preparations, and other conditions common to an oncology/hematology clinic environment Salary DOE – $25.

33 - $36.73 Benefit Information https://careers.usoncology.com/benefits Have knowledge and represent the research program in all regulatory affair requirements, interacting with local, state and federal agencies. Submissions of regulatory documents including but not limited to: initial IRB forms, 1572 forms, financial disclosures, annual reviews, amendments, investigational new drug applications, device related trial submissions, safety reports, and continuing reviews.

Track submissions and ensure timely filing of documents. Responsible for organizing and maintaining up to date clinical trial information, including study protocols and informed consent forms, for accurate presentation to physicians and study staff to ensure patient safety. Directly communicates with sponsors, study staff and Institutional Review Board Coordinators as it relates to study specific document modifications and Institutional Review Board requested revisions.

Tracking staff training to all applicable regulatory requirements including but not limited to GCP, Human subjects’ protection, hazmat ( IATA) training, and all study specific related training. Help to create/develop CCNW standard operating procedures to ensure staff understanding of required compliance and research participant safety.

Must be detail-oriented and be able to multi-task to meet standard response times and deadlines. Must be able to demonstrate appropriate conflict resolution in stressful situations. Demonstrate superior customer service skills. Demonstrate the ability to work independently and as part of a team. Any other duty as assigned.

Bachelor’s degree or equivalent combination of education and experience. Proficient with Microsoft Office It is preferred an individual has: Regulatory experience in clinical research Oncology experience Physical Demands: Regularly: stand, walk, grasp, reach, talk, and hear Occasionally : lift to 40 pounds, pull/push up to 40 pounds, carry up to 40 pounds, bend, and stoop/crouch Vision: clearly see up to 5 feet with or without corrective lenses Work Environment: While performing the essential duties/responsibilities of this job, the employee will: not be exposed to any workplace environmental conditions caused by extreme noise, heat, cold, workplace hazards, or atmospheric dust/fumes/vapors/mists be exposed to blood borne pathogens be exposed to toxic or caustic chemicals be exposed to ionizing radiation, medical preparations, and other conditions common to an oncology/hematology clinic environment Salary DOE – $25.

33 - $36.73 Benefit Information https://careers.usoncology.com/benefits