MCKESSON
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 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 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.
As the
Clinical Research Coordinator
you
are
responsible for
overall clinical operations of the facility’s research program including enrollment, regulatory, quality, and site operations. You will support
enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.
You will r
eview
the study design and inclusion/exclusion criteria with physician
s
and patient
s
You will ensure
the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
You will collect, complete, and enter
data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines
You will ensure
the integrity of the data
submitted
on case report forms or other data collection tools by
careful source document review and monitoring
data for missing or implausible data
You will c
r
eate
study specific tools for source documentation when not provided by sponsor
You will generate and track
drug shipments, lab ki
ts, and other supplies
You will
be
r
esponsible for
accurate
and complete documentation of protocol requirements acco
rding to site work instructions and standard operating procedures (
SOPs
)
You will track and report
adverse events, serious adverse events, protocol waivers, and deviations
You will
maintain
accurate
and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications
You will coordinate
regular site research meetings
You will attend
study-specific on-site meetings/visits, investigator meetings, conference calls, and other co
ordinator meetings, as
required
and you will work
closely with monitors, study teams and site staff to ensure quality study data
You will communicate
site status through a weekly activity report to
appropriate site/management
colleagues
You should have: An
Associate’s Degree
, preferably a
Bachelor’s Degree
Knowledge of m
edical and research terminology
Knowledge of
FDA Code of Federal Regulations and GCP
Knowledge of the c
linical research processes
Public presentation skills
The ability to m
anage multiple ongoing priorities and projects
with a diverse team of professionals
This position will be open for applications until January 30th.
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.
Please
click here
to learn more about our research offerings.
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. For more information regarding benefits through our parent company, McKesson, please
click here .
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.
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 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 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.
As the
Clinical Research Coordinator
you
are
responsible for
overall clinical operations of the facility’s research program including enrollment, regulatory, quality, and site operations. You will support
enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.
You will r
eview
the study design and inclusion/exclusion criteria with physician
s
and patient
s
You will ensure
the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
You will collect, complete, and enter
data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines
You will ensure
the integrity of the data
submitted
on case report forms or other data collection tools by
careful source document review and monitoring
data for missing or implausible data
You will c
r
eate
study specific tools for source documentation when not provided by sponsor
You will generate and track
drug shipments, lab ki
ts, and other supplies
You will
be
r
esponsible for
accurate
and complete documentation of protocol requirements acco
rding to site work instructions and standard operating procedures (
SOPs
)
You will track and report
adverse events, serious adverse events, protocol waivers, and deviations
You will
maintain
accurate
and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications
You will coordinate
regular site research meetings
You will attend
study-specific on-site meetings/visits, investigator meetings, conference calls, and other co
ordinator meetings, as
required
and you will work
closely with monitors, study teams and site staff to ensure quality study data
You will communicate
site status through a weekly activity report to
appropriate site/management
colleagues
You should have: An
Associate’s Degree
, preferably a
Bachelor’s Degree
Knowledge of m
edical and research terminology
Knowledge of
FDA Code of Federal Regulations and GCP
Knowledge of the c
linical research processes
Public presentation skills
The ability to m
anage multiple ongoing priorities and projects
with a diverse team of professionals
This position will be open for applications until January 30th.
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.
Please
click here
to learn more about our research offerings.
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. For more information regarding benefits through our parent company, McKesson, please
click here .
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.