New · posted Nov 1
IQVIA · Biotechnology
Sr. CRA, Oncology, IQVIA Biotech
- Durham, NC
- On-site
- Full-time
- Senior & Principal
The role
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Hiring Senior Clinical Research Associates
We are seeking an experienced Senior Clinical Research Associate to join our Clinical Monitoring team. In this role, you will independently manage and monitor clinical trial sites to ensure studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, regulatory requirements, and sponsor expectations.
As a key member of the study team, you will perform site monitoring activities including site qualification, initiation, routine monitoring, and closeout visits. You will partner closely with investigative sites to support patient recruitment and retention efforts, provide protocol and study-related training, and proactively identify and resolve quality or compliance issues.
The Sr CRA is responsible for overseeing site performance, tracking study milestones, reviewing source documentation, managing data query resolution, ensuring regulatory and essential documents are maintained, and documenting monitoring activities through timely and accurate reports. You will collaborate with cross-functional teams to support the successful execution of clinical trials and may mentor junior CRAs through co-monitoring and training activities.
What you need
- Bachelor’s degree in a scientific, healthcare, or related discipline (or equivalent combination of education and experience).
- Minimum of 4 years of on-site clinical monitoring experience.
- Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes.
- Experience conducting monitoring visits across multiple phases of clinical research.
- Excellent organizational, communication, and problem-solving skills.
- Ability to effectively manage multiple priorities in a fast-paced environment.
- Proficiency with Microsoft Office applications and clinical trial systems.
Preferred Skillsnice to have
- Strong therapeutic area knowledge and protocol management experience.
- Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams.
- Experience mentoring or supporting the development of junior clinical research professionals.
Join us in helping accelerate the development of innovative therapies that improve patient lives worldwide.
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 $105,100.00 - $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.
Pay and benefits
$105,100 – $197,500 a year
Employer providedHealth and welfare benefits
Incentive plans
Bonuses
Where you'll work
Durham, NCOn-siteOpen in Maps (opens in a new tab)
More jobs in Durham, NCEqual 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 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 22% above the US median for Clinical Research roles at this level.
This roleEmployer provided
Senior & Principal roles in the US50 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $105,100 | — | $197,500 |
| All US (middle half) | $123,750 | $124,500 | $130,500 |
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 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 193 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 18 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct10
- Collaboration and leadership6
- GMP and compliance3
- Investigations and CAPA2
- Validation and qualification2
- Documentation and SOPs1
- Data and digital systems1
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%
More roles at IQVIA
- View role
Clinical Research Coordinator
Bountiful, UTAssociate & SpecialistPharmaceuticals$37K–$91K
- View role
Clinical Research Associate 2
Durham, NCAssociate & SpecialistPharmaceuticals$75K–$198K
- View role
(Senior) Clinical Research Associate
Durham, NCAssociate & SpecialistPharmaceuticals$90K–$175K
- View role
Clinical Research Associate II
Durham, NCAssociate & SpecialistPharmaceuticals$75K–$198K
Similar Clinical Research roles elsewhere
- View role
Clinical Research Associate/Senior Clinical Research Associate- FSP
ParexelRemote, US NortheastSenior & PrincipalBiotechnologySalary not listed
- View role
Senior Clinical Research Associate
ICONRemote, USSenior & PrincipalBiotechnologySalary not listed
- View role
Senior Clinical Research Associate
ICONLos Angeles, CA · HybridSenior & PrincipalBiotechnology$111K–$138K
- View role
Sr. CRA - Phase 1 Oncology West Coast
ICONRemote, USSenior & PrincipalBiotechnology$111K–$138K
Sr. CRA, Oncology, IQVIA Biotech at IQVIA
Open until filled. $105K–$198K a year, employer provided.