Job Summary

The Research Compliance Coordinator must be knowledgeable of standard research and oncology care practices. The Research Compliance Coordinator advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.

Essential Duties and Responsibilities

Essential and other important responsibilities and duties may include but are not limited to the

following:

Protocol Compliance

• Reviews and comprehends the research protocol

• Adheres to applicable federal, state, and institutional regulations, policies, and procedures

related to clinical research

• Complies with NEXT Oncology SOPs

• Develops and maintains source documents, templates, or forms in a timely fashion.

• Ensure all protocol requirements have been captured on site specific forms, documents,

or templates.

• Assesses protocol for discrepancies or questions to ensure accurate source documents

and forms are created

• Assess and update forms for protocol amendments or protocol clarification letters

• Assess and update forms when issues are identified during the course of patient

treatments

• Participates in quality control activities to ensure data integrity, including timely

responses to database or sponsor queries

• Provide monthly reports to team to ensure compliance with protocol specified task

Knowledge, Skills and Abilities

• Bilingual in English/Spanish, preferred

• Knowledge of appropriate software including Microsoft Word, Excel, and Outlook,

Microsoft PowerPoint and Adobe Acrobat

• Attention to detail, organizational and accuracy skills

Required Education and Experience

• Current State Registered Nursing License for RNs

• Bachelor’s degree required for non-RNs

• Oncology clinical trial experience preferred

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 $47,400.00 - $118,600.00. 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.