Clinical Research Coordinator II-2

Meharry Medical College; Mission (KS); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator II-2 to lead advanced clinical research projects. This role involves ensuring compliance with regulations, managing financial aspects, and supporting operational functions. Ideal candidates will possess a strong background in clinical research practices, excellent data entry skills, and the ability to work under pressure. Join a dynamic team dedicated to advancing clinical and translational research, where your contributions will directly impact patient care and research outcomes. This opportunity offers a chance to grow in a supportive environment while making a meaningful difference in the field.

Qualifications

• Bachelor’s or master’s degree in a science discipline from an accredited program.
• Prior clinical research experience preferred in a patient care setting.

Responsibilities

• Coordinate advanced clinical research projects ensuring compliance with regulations.
• Manage financial aspects including budgets, revenue, and expenses.
• Assess eligibility of potential subjects through screening and interviews.

Skills

Clinical research practices

Data entry skills

Judgment skills

Teamwork

Education

Bachelor's degree in a science discipline

Master's degree in a science discipline

Tools

Personal computers

Job description

The Clinical Research Coordinator II-2 position involves coordinating advanced clinical research projects with supervision, ensuring compliance with regulations, and supporting operational and financial functions of the Center of Excellence for Clinical and Translational Research.

Essential Functions (Duties and Responsibilities):

1. Assess eligibility of potential subjects through screening interviews, reviews of medical records, discussions with physicians and nurses, and travel to participant locations for recruitment activities.
2. Maintain records of study activities, including case report forms, consent documentation, and regulatory forms.
3. Manage financial aspects such as budgets, revenue, expenses, invoices, and collections related to clinical research, including accounts receivable and payable.
4. Perform protocol-specific procedures like interviewing subjects, taking vital signs, performing electrocardiograms, and handling samples.
5. Monitor study activities for compliance with protocols and regulations.
6. Schedule appointments, inform patients or caregivers about study aspects, and ensure proper communication.
7. Assist with preparing IRB submissions, protocol revisions, and renewals, maintaining all IRB communications.
8. Perform other related duties as assigned.

Knowledge, Skills, and Abilities:

• Good working knowledge of clinical research practices.
• Proficiency with personal computers.
• Strong judgment skills in evaluating information.
• Accurate data entry and calculation skills.
• Ability to work under stress.
• Team-oriented attitude.

Education and Experience:

• Bachelor’s or master’s degree in a science discipline from an accredited program.
• Prior clinical research experience in a patient care setting preferred (e.g., LPN, travel phlebotomist, or clinical research experience).

Environmental Conditions and Physical Demands:

• Usual office environment.
• Manual dexterity, visual and auditory acuity.
• Ability to sit, stand, or walk for extended periods.