Monitor and assist with queries from internal colleagues, sponsors, and CROs. * Oversee inventory ... Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
Monitor and assist with queries from internal colleagues, sponsors, and CROs. * Oversee inventory ... Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
Monitor and assist with queries from internal colleagues, sponsors, and CROs. * Oversee inventory ... Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
Monitor and assist with queries from internal colleagues, sponsors, and CROs. * Oversee inventory ... Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
Monitor and assist with queries from internal colleagues, sponsors, and CROs. * Oversee inventory ... Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
Monitor and assist with queries from internal colleagues, sponsors, and CROs. * Oversee inventory ... Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
The Senior Clinical Research Associate-RN is responsible for performing data abstraction ... * Assist in the development of ongoing review of departmental/divisional standard operating ...
The Senior Clinical Research Associate-RN is responsible for performing data abstraction ... * Assist in the development of ongoing review of departmental/divisional standard operating ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
... * Assist in the development and maintenance of the knowledge base and data entry practices to ... Trains clinical research staff on e-research applications, how to incorporate and manage the e ...
... * Assist in the development and maintenance of the knowledge base and data entry practices to ... Trains clinical research staff on e-research applications, how to incorporate and manage the e ...
... * Assist in the development and maintenance of the knowledge base and data entry practices to ... Trains clinical research staff on e-research applications, how to incorporate and manage the e ...
... * Assist in the development and maintenance of the knowledge base and data entry practices to ... Trains clinical research staff on e-research applications, how to incorporate and manage the e ...
Clinical Research Coordinator I - Nurse
Cordova, TN · On-site
$60K - $75K/yr
Clinical Research Coordinator I - Nurse Iterative Health is a healthcare technology and services ... Participate actively in communication of status and results to management * Assist with routine ...
Clinical Research Coordinator I - Nurse
Cordova, TN · On-site
$60K - $75K/yr
Clinical Research Coordinator I - Nurse Iterative Health is a healthcare technology and services ... Participate actively in communication of status and results to management * Assist with routine ...
Clinical Research Coordinator I - Nurse
Cordova, TN · On-site
$60K - $75K/yr
Clinical Research Coordinator I - Nurse Iterative Health is a healthcare technology and services ... Participate actively in communication of status and results to management * Assist with routine ...
Clinical Research Coordinator I - Nurse
Cordova, TN · On-site
$60K - $75K/yr
Clinical Research Coordinator I - Nurse Iterative Health is a healthcare technology and services ... Participate actively in communication of status and results to management * Assist with routine ...
... * Assist in the development and maintenance of the knowledge base and data entry practices to ... Trains clinical research staff on e-research applications, how to incorporate and manage the e ...
... * Assist in the development and maintenance of the knowledge base and data entry practices to ... Trains clinical research staff on e-research applications, how to incorporate and manage the e ...
Clinical Research Coordinator I - Nurse
Cordova, TN · On-site
$60K - $75K/yr
Clinical Research Coordinator I - Nurse Iterative Health is a healthcare technology and services ... Participate actively in communication of status and results to management * Assist with routine ...
Quick apply
Clinical Research Coordinator I - Nurse
Cordova, TN · On-site
$60K - $75K/yr
Clinical Research Coordinator I - Nurse Iterative Health is a healthcare technology and services ... Participate actively in communication of status and results to management * Assist with routine ...
Oncology Clinical Research Nurse
$75K - $102K/yr
Clinical research experience preferred but not required * Strong understanding of patient safety ... Accrual Rates: * Length of service determines the rate at which the team member will accrue PTO.
Quick apply
Oncology Clinical Research Nurse
$75K - $102K/yr
Clinical research experience preferred but not required * Strong understanding of patient safety ... Accrual Rates: * Length of service determines the rate at which the team member will accrue PTO.
Oncology Clinical Research Nurse
Nashville, TN · On-site
$75K - $102K/yr
Clinical research experience preferred but not required * Strong understanding of patient safety ... Accrual Rates: • Length of service determines the rate at which the team member will accrue PTO.
Oncology Clinical Research Nurse
Nashville, TN · On-site
$75K - $102K/yr
Clinical research experience preferred but not required * Strong understanding of patient safety ... Accrual Rates: • Length of service determines the rate at which the team member will accrue PTO.
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Senior Clinical Research Associate
Knoxville, TN · On-site +1
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Senior Clinical Research Associate
Knoxville, TN · On-site +1
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Quick apply
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Quick apply
Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... A clinical research professional with 3+ years of on-site monitoring experience in the ...
Research Assistant I (Psychology)
Nashville, TN · On-site
$18.50 - $25.50/hr
JOB SUMMARY Clinical Research Assistant in the Vanderbilt Center for Cognitive Medicine. Full-time on-site clinical research assistant will support clinical research focused on geriatric depression ...
Research Assistant I (Psychology)
Nashville, TN · On-site
$18.50 - $25.50/hr
JOB SUMMARY Clinical Research Assistant in the Vanderbilt Center for Cognitive Medicine. Full-time on-site clinical research assistant will support clinical research focused on geriatric depression ...
Clinical Research Coordinator III
Nashville, TN · Hybrid
$23.50 - $31.25/hr
Supervise research assistants, coordinators, and interns * Conduct onboarding, training, and ... Clinical Research (Advanced): Knows what job-related resources are available throughout the company.
Clinical Research Coordinator III
Nashville, TN · Hybrid
$23.50 - $31.25/hr
Supervise research assistants, coordinators, and interns * Conduct onboarding, training, and ... Clinical Research (Advanced): Knows what job-related resources are available throughout the company.
Assistant Clinical Research Rater information
What is the difference between Assistant Clinical Research Rater vs Clinical Research Coordinator?
| Aspect | Assistant Clinical Research Rater | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | High school diploma or equivalent; some roles may require a bachelor's degree | Bachelor's degree in health sciences or related field; certification often preferred |
| Work Environment | Remote or in clinical settings; primarily data review and assessments | Clinical sites; managing study logistics and participant coordination |
| Employer & Industry Usage | Research organizations, pharmaceutical companies, universities | Hospitals, research institutions, pharmaceutical companies |
| Common Search & Comparison Intent | Understanding entry-level roles in clinical research | Managing clinical trials and participant interactions |
The Assistant Clinical Research Rater typically focuses on reviewing and assessing data, often working remotely, with minimal direct patient interaction. In contrast, the Clinical Research Coordinator manages the overall conduct of clinical trials, including participant recruitment and site management. Both roles are essential in clinical research but differ in responsibilities, required credentials, and work environment.
McKesson rating
7.9
Based on 209 frontline employees who took The Breakroom Quiz
48th of 86 rated pharmaceutical
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 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 Sr. Manager of Clinic Research Services, you will be responsible for execution of strategy for Clinical Research teams including clinic research care, clinic research nurse, and clinical support service teams. This includes creation of goals and supporting overall departmental status with defined metrics. Responsible for overall daily operations as well as hiring and developing managers and colleagues of these respective teams. Responsibilities include:
Provide direct supervision and development of the Manager Clinical Research Nurses, Manager Research Care Support, and Manager Clinical Support Services
Provide oversight, leadership, and support of organizational processes during study activation and maintenance of trials to ensure the delivery of quality research compliance.
Monitor and assist with queries from internal colleagues, sponsors, and CROs.
Oversee inventory and evaluate acquisition of study supplies required.
Develop, maintain, and report out performance metrics and expectations to leadership on a regular basis for the research nurse, research care, and clinical support services teams.
Provide clinical research nurses, research care, and clinical, support for site audits and CAPAs.
Build and manage strategic internal and external relationships.
Meet with the Director weekly to communicate key issues, progress, and risks related to laboratory, research care, and clinical support services.
Meet with SCRI Oncology Partners, TCMC, and other external leaders regarding clinical support for research patients and develop/optimize processes as needed.
Meet with the SCRI site leadership team as needed on strategies for process improvement and strategic initiatives, execute, and monitor progress for clinical research nurses, research care, and clinical support services teams.
Assist in the creation, development, maintenance, and execution of SOPs, WIs, job aids.
Complete protocol training per standard operating procedure.
Attend staff and other assigned meetings.
Maintain patient confidentiality according to ethical and legal requirements.
Adhere to appropriate Standard Operating Procedures.
You should have for this position:
An Associate Degree, Bachelor Degree preferred
At least one year of experience working in Clinical Research.
Registered Nurse preferred
At least one year of experience working in oncology.
Working knowledge of clinical trials protocol
General knowledge of Regulatory Research and Quality Assurance guidelines
Skills in communication with physicians and internal/external stakeholders
Public presentation skills
Ability to communicate and collaborate effectively with a diverse team of professionals.
Ability to critically think and problem solve situations as they arise.
Adaptable to the changing needs of the team and work environment
Ability to self-direct, including prioritization of multiple simultaneous tasks
Strong interpersonal and organizational skills
Certified Clinical Research Professional (CCRP) preferred.
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 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. 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.
About McKesson Medication Management
Sourced by ZipRecruiter
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
San Francisco, CA, US
Year founded
2014