Clinical Research Assistant

Pinnacle Clinical Research- A Summit Solution; Austin (TX); On-site; USD 46,000 - 65,000; Full time

Job summary

Pinnacle Clinical Research- A Summit Solution in Austin, TX seeks a candidate to support the Clinical Research Coordinator and the principal investigator with study activities, patient coordination, and regulatory documentation. You will handle scheduling, data entry, and reporting while maintaining confidentiality.

Responsibilities include preparing study materials, assisting with regulatory submissions, liaising with sponsors and sites, and ensuring compliance with FDA, ICH-GCP, HIPAA, and IRB

Qualifications

• High school diploma or GED; or 2–4 years related experience
• Knowledge of medical terminology
• Experience with clinical trial documentation and regulatory submissions

Responsibilities

• Assist with study documents and new study prep
• Maintain regulatory files and assist with submissions
• Serve as secondary liaison with sponsors
• Prepare for monitor visits and create reports
• Conduct patient assessments and coordinate visits
• Support subject screening and recruitment
• Update CTMS and other study systems
• Coordinate multiple projects with competing priorities

Skills

Oral communication

Written communication

Organizational skills

Attention to detail

Medical terminology

Diplomatic communication

Flexibility with changing priorities

Education

High school diploma or GED

Tools

Microsoft Word

Microsoft Excel

Browsers (IE/Chrome/Firefox)

CTMS

eCRF systems

Job description

Summary: Assists the Clinical Research Coordinator and the principal investigator with administering activities to facilitate clinical research, which may include working with an affiliate or collaborating research sites. Exercises judgment within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the study Investigator and supervisor. Always maintains subject and document confidentiality, understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards (IRB), and institutional policies and procedures by performing the following duties.

Duties and Responsibilities:

• Assists with the creation and completion of study related documents and new study preparation.
• Assists with the completion of regulatory submissions and maintains regulatory files as directed.
• Acts as a secondary liaison with sponsors.
• Assists with the preparation for study monitor visits as directed.
• Creates reports as requested.
• Completes study directed assessments with patients to include, but not limited to adverse events, test article (TA) handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessment.
• Assists with subject screening and recruitment as directed.
• Updates Clinical Trial Management Software (CTMS) as directed.
• Coordinates multiple projects with competing priorities and deadlines, as needed based on clinical trial protocol directives and study volume.
• Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients.

Duties, responsibilities, and activities may change, or new ones assigned at any time.

Education Experience:

High school diploma or general education degree (GED); or two to four years related experience and/or training; or equivalent combination of education and experience.

Certificates and Licenses:

• Clinical research certification preferred

Knowledge, Skills, and Other Abilities:

• Ability to demonstrate competence in oral and written communication
• Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor
• Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
• Medical knowledge, including medical terminology
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
• Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems.

Work Environment and Physical demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Work is performed in an office/laboratory and/or a clinical environment.
• Exposure to biological fluids and/or bloodborne pathogens.
• Personal protective equipment required such as protective eyewear, garments, and gloves.
• Occasional travel may be required domestic and/or international.
• Ability to work in an upright and/or stationary position for 6-10 hours per day.
• Frequent mobility required.
• Occasional squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.