Clinical Research Coordinator II

Overview:

Job Title: Clinical Research Coordinator

Employment Type: Full-Time (40 hours per week)
Schedule: Monday to Friday, No evenings, weekends, or holidays

Company Overview:
Join Missouri Cancer Associates, a prestigious healthcare practice renowned for its specialization in medical oncology, hematology, radiation oncology, and urology. With a legacy of excellence spanning over 40 years, we are committed to delivering superior patient care across ten communities in Missouri. Our team comprises 22 skilled providers, including physicians and nurse practitioners, dedicated to utilizing state-of-the-art technology to enhance patient outcomes. As the premier Cancer Treatment Center in Mid-Missouri, we invite you to be part of our exciting journey.

Why Work with Us?

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

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.

Qualifications:

Education/Training:
Associate degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Minimum of one year of experience in a clinical or scientific discipline, oncology experience preferred.
Business Experience:
Proficiency in Microsoft Office.
Experience working with physicians is preferred.
Specialized Skills:
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.

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.

This job description provides a general overview and is not an exhaustive list of all responsibilities. Additional duties may be assigned as necessary to meet company objectives. Reasonable accommodations will be provided to individuals with disabilities to perform essential functions.

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