Research Coordinator

Ohio Gastroenterology Group.; Columbus (OH); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading healthcare organization in Columbus is seeking a Research Coordinator to manage and facilitate gastroenterology clinical research studies. The ideal candidate should have a strong clinical background, exceptional organizational skills, and the ability to effectively communicate with patients and research teams. This full-time position offers a dynamic work environment and the opportunity to contribute to important research initiatives.

Qualifications

• 3+ years previous experience as a clinical research coordinator for pharmaceutical phase II or III trials required.
• Effective communication skills including written, verbal and presentation skills.
• Strong attention to detail, organizational, analytical, and problem-solving skills.

Responsibilities

• Administratively and clinically manage industry sponsored clinical trials.
• Assist with protocol design and patient recruitment through detailed chart reviews.
• Perform blood draws, process specimens and schedule patient research visits.

Skills

Communication

Organization

Attention to Detail

Analytical

Problem-Solving

Education

Associates degree in a clinical or scientific related discipline

Bachelor's degree preferred

Tools

Microsoft Word

Excel

Power Point

CTMS

EMR

Job description

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Job Objective: The Research Coordinator will facilitate all facets of GI clinical research studies.

Duties And Responsibilities

Administratively and clinically manage industry sponsored clinical trials

Assist with protocol design, where requested

Adhere to Research SOP's, Good Clinical Practices and the study protocols

Assist in patient recruitment by performing detailed chart reviews and patient interviews

Discuss study protocols with patients and verify the informed consent documentation

Review Medical History of patient against Inclusion/Exclusion Criteria of studies

Perform blood draws, process and ship blood/urine specimens per study protocol and IATA regulations

Schedule all patient research visits and procedures consistent with protocol requirements

Dispense study medication, collect vital signs and perform ECGs

Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol

Ensure the filing and maintenance of all regulatory documents

Schedule and prepare for monitor visits

Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy

Qualifications

Associates degree in a clinical or scientific related discipline required, Bachelor's degree preferred

3+ years previous experience as a clinical research coordinator for pharmaceutical phase II or III trials, GI trials experience preferred

Computer skills - Microsoft Word, Excel, Power Point, CTMS, EMR

Previous experience in a role of complex administration or project coordination

Effective communication skills to include written, verbal and presentation skills

Strong attention to detail and organizational, analytical, and problem-solving skills

Periodic local travel to other practice locations on an as-needed basis

Physical Requirements

Ability to stand and walk throughout the day

Prolonged periods of sitting and performing administrative duties including the use of computers

Ability to bend, twist, stoop, and reach

Able to lift and carry supplies and equipment as needed (up to 15 pounds)

Physical Demands

Applies the principles of body mechanics in lifting or moving charts, boxes, or equipment (occasional)

Must be able to independently lift 25 pounds (occasional)

Must be able to sit (frequent), stand (frequent), walk (frequent), stoop (frequent), bend over (frequent), and type on keyboard (frequent).

Work Environment

Medical office requiring some contact with adult patients

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Required

Preferred

Job Industries

• Other

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Medical Practices

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