New · posted Nov 1
IQVIA · Pharmaceuticals
Clinical Research Associate, Sponsor Dedicated, Oncology
- Remote, US
- Remote
- Full-time
- Associate & Specialist
The role
Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.
What you need
- Education: BS Degree in a scientific discipline or healthcare preferred.
- Experience: Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.
- Knowledge: Strong understanding of GCP and ICH guidelines, with expertise in oncology protocols.
- Skills: Proficiency in Microsoft Office, excellent communication skills, and strong organizational and problem-solving abilities.
- Attributes: Effective time and financial management, and the ability to build strong working relationships.
Why Join Us? Be part of a team that’s driving innovation in clinical research. Your contributions will help shape the future of healthcare. Apply now and embark on a rewarding career journey with us!
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 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 $90,200.00 - $197,500.00. 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.
What you'll do
- Site Visits: Conduct selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Recruitment Drive: Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.
- Training & Communication: Provide protocol training and maintain regular communication with sites to manage expectations and address issues.
- Quality Assurance: Evaluate site practices for protocol adherence and escalate quality issues as needed.
- Study Progress: Track regulatory submissions, recruitment, enrollment, and data management to ensure smooth study progress.
- Documentation: Maintain essential documents in the Trial Master File (TMF) and Investigator’s Site File (ISF) as per regulatory requirements.
- Mentorship: Mentor clinical staff through co-monitoring and training visits.
- Collaboration: Work closely with study team members to support project execution.
- Financial Management: Manage site finances and retrieve invoices as per local requirements.
Pay and benefits
$90,200 – $197,500 a year
Employer providedHealth and welfare benefits
Incentive plans
Bonuses
Equal opportunity, accessibility and legal noticesIQVIA's statements, word for word
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
Job intelligence
The context around this role
Live data · November 3, 2026
Salary intelligence
How the pay compares
This role's midpoint is 39% above the US median for Clinical Research roles at this level.
This roleEmployer provided
Associate & Specialist roles in Kansas6 roles publishing pay
Associate & Specialist roles in the US62 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $90,200 | — | $197,500 |
| Kansas (middle half) | $128,500 | $135,500 | $139,125 |
| All US (middle half) | $92,750 | $103,250 | $126,125 |
This role: IQVIA's own published range. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 210 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not IQVIA's own promotion track.
Career resources on Clinical Research
Skills DNA
What this role leans on
How many of the posting's 19 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct8
- Collaboration and leadership6
- GMP and compliance2
- Data and digital systems2
- Documentation and SOPs1
- Investigations and CAPA1
- Validation and qualification1
- Regulatory submissions1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
IQVIA on Regulatory Jobs
- 83
- Open roles
- 59
- Distinct roles
- 26
- Locations
By discipline
- Clinical72 87%
- Regulatory7 8%
- Quality4 5%
By level
- Associate & Specialist43 52%
- Manager15 18%
- Senior & Principal15 18%
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Clinical Research Associate, Sponsor Dedicated, Oncology at IQVIA
Open until filled. $90K–$198K a year, employer provided.