Research Coordinator

North Texas Institute of Neurology and Headache, PA; Plano (TX); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading medical practice is seeking a Clinical Research Coordinator to manage clinical trials focused on migraines and multiple sclerosis. In this entry-level role, you will coordinate with participants, ensure regulatory compliance, and oversee data management. Ideal candidates will have strong communication skills and 1 to 2 years of relevant research experience.

Benefits

Medical, dental and vision

PTO

401k plus matching after 1 year of employment

Paid major holidays

Qualifications

• 1-2 years of research experience required.
• Knowledge of clinical research terminology and regulations.
• Ability to work with confidential information.

Responsibilities

• Interact with clinical research participants and coordinate documentation.
• Conduct research procedures according to protocol and maintain data.
• Monitor patient safety and report according to standards.

Skills

Computer Skills

Communication Skills

Problem Solving

Job description

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Research Coordinator Job Description

NTINH is seeking a Clinical Research Coordinator for our clinical research program. The prospective applicant will be involved in clinical trials focused on migraines and multiple sclerosis. One to two years of research experience is required.

Research Coordinator Job Description

NTINH is seeking a Clinical Research Coordinator for our clinical research program. The prospective applicant will be involved in clinical trials focused on migraines and multiple sclerosis. One to two years of research experience is required.

Job Duties

May perform some or all the following:

Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures).

Interacts via telephone, telehealth or in-person.

Coordinates regulatory documentation for research studies that includes maintaining information to comply with industry standards, and FDA requirements.

Coordinates and schedules procedures as per research study.

Screens, recruits, enrolls and follows subjects according to research protocol guidelines (non-clinical and clinical procedures).

May also assist with the consent processes. Maintains and coordinates data collection information required for each study.

Conducts research procedures according to the protocol with proper training and check offs to maintain scope of service.

Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards.

Enters data or assists in assembling data to enter in the assigned clinical trial management system, and/or other required data entry systems.

Maintains required subject documentation for each study protocol.

Knowledge, Skills & Abilities

Work requires knowledge of basic and clinical research terminology, regulations, and procedures.

Work requires strong computer skills (spreadsheets, databases, and interactive web-based software)

Work requires ability to communicate effectively with various levels of internal and external contacts.

Work requires ability to work with confidential information on daily basis

Proactively works to maximize results of the team and organization

Follows and understands the regulations for Protected Health Information (PHI)

Work requires good communication skills.

Work requires the ability to problem solve.

Benefits:

Medical, dental and vision

PTO

401k plus matching after 1 year of employment

Paid major holidays.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Medical Practices

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