McKesson
Be among the first 25 applicants.
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 become part of one of the largest community‑based cancer programs advancing oncology treatments and improving outcomes for cancer patients worldwide. We look for mission‑driven candidates who want to advance the fight against cancer and make a difference in patients’ lives.
Our Mission
People 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 passionate caregivers, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.
Study Coordinator Responsibilities
You will lead the execution of trials for the research team.
You will plan and track all assigned clinical activity throughout the startup, interim, and close‑out phases.
You will confirm patient eligibility and discuss discrepancies with nursing staff and physicians.
You will verify that study procedures are performed within the protocol‑specified window.
You will participate in teleconferences with sponsors to update on patients, including research visits, toxicity, and overall response. Responsible for notifying the department before and after calls to update study staff.
You will present in weekly protocol meetings to investigators, research staff, and management.
You will provide pertinent safety information to sponsor and study teams by monitoring patient toxicity, including serious adverse events, according to Common Toxicity Criteria.
You will update internal research teams on protocol modifications and specifications, including visit schedule, assessment windows, dose modifications, and laboratory assessments.
You will create study‑specific tools for source documentation, including eligibility worksheets, screening checklists, and worksheets capturing vital signs and blood sampling (as applicable).
You will ensure study‑specific tools, including source documents (paper and/or EMR), are updated with any amendments or study changes.
You will investigate the root cause of major protocol deviations and manage follow‑up with responsible departments for corrective and preventative actions.
You will ensure the pharmacy has Investigative Product and supplies.
You will interface with the laboratory technician for lab kits and processing.
You will track and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
You will participate in monitor visits for each assigned trial at each monitoring visit.
You will review and comment on monitor letters within five business days of receipt and ensure resolution of open items.
You will review source documentation and queries for missing documentation.
You will collect, complete, and enter data into study‑specific case report forms or electronic data capture systems within the contractually agreed timeframe.
You will maintain case report form tracking management database.
You will review trial data for clinical relevance and answer appropriate queries, apprising research scientists and the management team of all study‑specific medical issues for guidance.
You will assist in ensuring physician oversight by updating on protocol issues and obtaining signatures and clinical significance of laboratory reports, ECGs, and adverse events.
You will assist in external sponsor audit and US FDA inspection preparation, conduct, and close‑out processing.
You will review and respond to audit findings and escalate issues.
You will maintain and archive study documentation and correspondence per company policy.
You will report patient visit and data entry information to the financial tracking system.
You will provide required metrics to leadership.
You will initiate improvements to enhance the efficiency and quality of work performed on assigned projects.
You will adhere to professional standards and SOPs established for clinical research.
You will assist the internal quality team in preparation for sponsor and US FDA audit teams.
Qualifications
Understanding of clinical trial data.
Knowledge of FDA guidelines and GCP is required.
Ability to work independently in a fast‑paced environment.
Interpersonal skills, detail‑oriented and meticulous.
Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel.
Bachelor’s Degree is preferred.
At least one year of experience in healthcare, research, or another science‑related field.
At least one year of experience planning and managing the clinical trial process.
This position will be open for applications until January 20, 2026.
About Sarah Cannon Research Institute
Sarah 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 750 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 today. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 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.
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.
#J-18808-Ljbffr
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 become part of one of the largest community‑based cancer programs advancing oncology treatments and improving outcomes for cancer patients worldwide. We look for mission‑driven candidates who want to advance the fight against cancer and make a difference in patients’ lives.
Our Mission
People 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 passionate caregivers, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.
Study Coordinator Responsibilities
You will lead the execution of trials for the research team.
You will plan and track all assigned clinical activity throughout the startup, interim, and close‑out phases.
You will confirm patient eligibility and discuss discrepancies with nursing staff and physicians.
You will verify that study procedures are performed within the protocol‑specified window.
You will participate in teleconferences with sponsors to update on patients, including research visits, toxicity, and overall response. Responsible for notifying the department before and after calls to update study staff.
You will present in weekly protocol meetings to investigators, research staff, and management.
You will provide pertinent safety information to sponsor and study teams by monitoring patient toxicity, including serious adverse events, according to Common Toxicity Criteria.
You will update internal research teams on protocol modifications and specifications, including visit schedule, assessment windows, dose modifications, and laboratory assessments.
You will create study‑specific tools for source documentation, including eligibility worksheets, screening checklists, and worksheets capturing vital signs and blood sampling (as applicable).
You will ensure study‑specific tools, including source documents (paper and/or EMR), are updated with any amendments or study changes.
You will investigate the root cause of major protocol deviations and manage follow‑up with responsible departments for corrective and preventative actions.
You will ensure the pharmacy has Investigative Product and supplies.
You will interface with the laboratory technician for lab kits and processing.
You will track and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
You will participate in monitor visits for each assigned trial at each monitoring visit.
You will review and comment on monitor letters within five business days of receipt and ensure resolution of open items.
You will review source documentation and queries for missing documentation.
You will collect, complete, and enter data into study‑specific case report forms or electronic data capture systems within the contractually agreed timeframe.
You will maintain case report form tracking management database.
You will review trial data for clinical relevance and answer appropriate queries, apprising research scientists and the management team of all study‑specific medical issues for guidance.
You will assist in ensuring physician oversight by updating on protocol issues and obtaining signatures and clinical significance of laboratory reports, ECGs, and adverse events.
You will assist in external sponsor audit and US FDA inspection preparation, conduct, and close‑out processing.
You will review and respond to audit findings and escalate issues.
You will maintain and archive study documentation and correspondence per company policy.
You will report patient visit and data entry information to the financial tracking system.
You will provide required metrics to leadership.
You will initiate improvements to enhance the efficiency and quality of work performed on assigned projects.
You will adhere to professional standards and SOPs established for clinical research.
You will assist the internal quality team in preparation for sponsor and US FDA audit teams.
Qualifications
Understanding of clinical trial data.
Knowledge of FDA guidelines and GCP is required.
Ability to work independently in a fast‑paced environment.
Interpersonal skills, detail‑oriented and meticulous.
Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel.
Bachelor’s Degree is preferred.
At least one year of experience in healthcare, research, or another science‑related field.
At least one year of experience planning and managing the clinical trial process.
This position will be open for applications until January 20, 2026.
About Sarah Cannon Research Institute
Sarah 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 750 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 today. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 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.
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.
#J-18808-Ljbffr