Clinical Research Protocol Educator - Remote US

McKesson; Nashville (TN); Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Total Rewards package

Competitive compensation

Job summary

Sarah Cannon Research Institute (SCRI) seeks a Clinical Research Protocol Educator to design, deliver, and evaluate training for clinical trial staff, primarily Research Nurses, with potential inclusion of coordinators and site personnel. This remote US-based role requires translating protocol information into engaging staff education and ensuring regulatory compliance.

You will lead training development, present materials, and support site start-up activities to improve trial conduct and

Qualifications

• An Associate Degree; Bachelor Degree preferred.
• Oncology knowledge across major cancer types and treatment options.
• Experience with clinical trials regulations (FDA/ICH) and IRB processes.
• At least one year of oncology and research experience.
• Certification (ACRP/CCRP) preferred; OCN preferred.

Responsibilities

• Attend Investigator and Site start up meetings and disseminate information to Clinical Operations staff.
• Develop and deliver training for new protocols and determine delivery timing/frequency.
• Create learning aids: guides, models, tutorials and reference materials for staff education.
• Develop presentations and facilitate groups, workshops to enhance site clinic knowledge.
• Complete regimen templates for HER systems for current and upcoming protocols; assist with other duties.

Skills

Oncology knowledge

Training delivery

Group facilitation

Regulatory knowledge

Education

Associate Degree

Bachelor Degree preferred

ACRP/CCRP Certification preferred

OCN Certification preferred

Job description

It’s More Than a Career, It’s a Mission.Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.Our MissionPeople who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.Job DescriptionAs the Clinical Research Protocol Educator you will direct the design, plan, delivery and evaluation of clinical trial related training activities of Sarah Cannon colleagues. Your training primarily includes Research Nurses but may also include Research Coordinators, non-clinical research staff, and Clinical Site personnel.This is a remote position based in the US; relocation assistance and visa sponsorship are not available.Duties include and are not limited to:You will attend and participate in Investigator and Site start up meetings with the responsibility to disseminate appropriate information to the Clinical Operations staffYou will develop and participate in the delivery of training for new protocols and determine the delivery mechanism, timing and frequencyYou will develop and utilize learning aids such as self-study guides, demonstration models, multimedia visual aids, computer tutorials and reference materials to educate and train applicable staffYou will develop presentations and facilitate groups, workshops and programs to enhance strategic site clinic and Sarah Cannon research staff knowledgeYou will complete regimen templates for HER systems for current and upcoming protocolsOther duties as assignedQualifications for success include:An Associate Degree; Bachelor Degree preferredExtensive oncology knowledge base of all major cancer types including disease-related symptom management, standard treatment options, and treatment-related side effect managementKnowledge of federal and state regulations and ICH guidelines pertaining to the conduct of clinical trials involving human subjects for Investigator and Sponsor requirementsKnowledge and understanding of the principles, processes, and ethical considerations in clinical trials involving human subjectsKnowledge of the guidelines, standards and operating requirements of Institutional Review BoardsAt least one year of oncology experienceAt least one year of research experienceResearch Certification (ACRP or CCRP) preferredOncology Certification (OCN) preferredAbout Sarah Cannon Research InstituteSarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves.As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.McKesson job postings are posted on our career site: careers.mckesson.com .We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.