Clinical Trial Assistant

IQVIA • San Antonio, TX

2d • $34,400 - $86,000

About The Position

Job Summary Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Review pathology reports from PK department to redact any require information. Review lab reports from the Data Management department to redact any required information. Review eligibility documentation and serious adverse event documentation. Redact the necessary information. Assist in redaction of Serious Adverse Event documentation for safety reporting. Assist in redaction and verification of all PHI removal from images within internal imaging portal (Nucleus). All other duties as assigned. Knowledge, Skills and Abilities Must be able to work independently and with a team. Must be able to complete assigned tasks in a timely manner. Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $34,400.00 - $86,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Requirements

• Must be able to work independently and with a team.
• Must be able to complete assigned tasks in a timely manner.
• High School Diploma required.
• Microsoft Office and Adobe experience required.

Nice To Haves

• Bachelor’s degree from an accredited university is preferred.
• Clinical Research experience preferred.
• Medical terminology preferred.

Responsibilities

• Review pathology reports from PK department to redact any require information.
• Review lab reports from the Data Management department to redact any required information.
• Review eligibility documentation and serious adverse event documentation.
• Redact the necessary information.
• Assist in redaction of Serious Adverse Event documentation for safety reporting.
• Assist in redaction and verification of all PHI removal from images within internal imaging portal (Nucleus).
• All other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED