Clinical Research Coordinator II/ Private Oncology Practice
The US Oncology Network, Columbia, MO, United States
Job Title
Clinical Research Coordinator
Employment Type
Full-Time (40 hours per week)
Schedule
Monday to Friday, No evenings, weekends, or holidays
Location
1705 E Broadway, Columbia, MO
Proudly affiliated with Urology Associates of Central Missouri and the US Oncology Network.
Position Overview
As a Clinical Research Coordinator I, you will play a pivotal role in the management and coordination of multiple clinical research studies. Your responsibilities will include patient screening for eligibility, participation in study visits, and ensuring protocol compliance. You will collaborate with physicians and other healthcare providers to conduct ongoing assessments and documentation, ensuring adherence to US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), Good Clinical Practice (GCP) principles, and applicable regulations.
Responsibilities
Screen and evaluate potential patients for protocol eligibility.
Present trial concepts and details to patients and facilitate the informed consent process.
Assist in patient care in accordance with protocol requirements, including investigational drug disbursement and accountability.
Participate in data collection, entry, and reporting.
Collaborate with physicians to monitor patient conditions, adverse events, and study drug responses.
Engage in required training, education, and auditing activities.
Assist with regulatory document maintenance and lab specimen logistics.
Education & Training
Associate degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Qualifications
Minimum of one year of experience in a clinical or scientific discipline, oncology experience preferred.
Proficiency in Microsoft Office.
Experience working with physicians is preferred.
Exceptional communication and organizational skills.
Strong multitasking and time management abilities.
Attention to detail and interpersonal skills for interacting with diverse individuals.
Ability to perform basic clinical assessments.
Benefits
Impactful Role: Contribute meaningfully to patient lives in a dynamic and supportive environment.
Competitive Benefits Package:
Medical, Dental, and Vision Insurance
Life Insurance and Short-Term Disability Coverage
401(k) Retirement Plan
Paid Time Off (PTO)
Wellness Program with Healthy Lifestyle Rewards
Working Conditions
Environment: Traditional office setting with exposure to conditions typical of an oncology/hematology clinic.
Physical Requirements
Extensive computer-based work.
Standing and walking for significant periods.
Occasionally lifting items up to 40 lbs.
Normal range vision and hearing required.
Reasonable accommodations will be provided to individuals with disabilities to perform essential functions.
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Clinical Research Coordinator
Employment Type
Full-Time (40 hours per week)
Schedule
Monday to Friday, No evenings, weekends, or holidays
Location
1705 E Broadway, Columbia, MO
Proudly affiliated with Urology Associates of Central Missouri and the US Oncology Network.
Position Overview
As a Clinical Research Coordinator I, you will play a pivotal role in the management and coordination of multiple clinical research studies. Your responsibilities will include patient screening for eligibility, participation in study visits, and ensuring protocol compliance. You will collaborate with physicians and other healthcare providers to conduct ongoing assessments and documentation, ensuring adherence to US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), Good Clinical Practice (GCP) principles, and applicable regulations.
Responsibilities
Screen and evaluate potential patients for protocol eligibility.
Present trial concepts and details to patients and facilitate the informed consent process.
Assist in patient care in accordance with protocol requirements, including investigational drug disbursement and accountability.
Participate in data collection, entry, and reporting.
Collaborate with physicians to monitor patient conditions, adverse events, and study drug responses.
Engage in required training, education, and auditing activities.
Assist with regulatory document maintenance and lab specimen logistics.
Education & Training
Associate degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Qualifications
Minimum of one year of experience in a clinical or scientific discipline, oncology experience preferred.
Proficiency in Microsoft Office.
Experience working with physicians is preferred.
Exceptional communication and organizational skills.
Strong multitasking and time management abilities.
Attention to detail and interpersonal skills for interacting with diverse individuals.
Ability to perform basic clinical assessments.
Benefits
Impactful Role: Contribute meaningfully to patient lives in a dynamic and supportive environment.
Competitive Benefits Package:
Medical, Dental, and Vision Insurance
Life Insurance and Short-Term Disability Coverage
401(k) Retirement Plan
Paid Time Off (PTO)
Wellness Program with Healthy Lifestyle Rewards
Working Conditions
Environment: Traditional office setting with exposure to conditions typical of an oncology/hematology clinic.
Physical Requirements
Extensive computer-based work.
Standing and walking for significant periods.
Occasionally lifting items up to 40 lbs.
Normal range vision and hearing required.
Reasonable accommodations will be provided to individuals with disabilities to perform essential functions.
#J-18808-Ljbffr