Full-time
Oncology Clinical Research Associate (CRA 2), Sponsor Dedicated
$72K/yr – $182K/yr
Overland Park, KSScience & PharmaceuticalPosted 18d ago
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Role overview
Job type
Salary
$72K/yr – $182K/yr
Location
Sector
Posted
18 days ago
Job description
Oncology Clinical Research Associate (CRA 2), Sponsor Dedicated jobs in United States
Tags
25+ applicants
Original Job Post
IQVIA
+2 more
$72K/yr - $182K/yr
0–2 years exp
93
STRONG MATCH
Experience Level
100
Skill
89
Responsibilities
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Collaborate and liaise with study team members for project execution support as appropriate
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Preferred
Cardiovascular/Renal/Metabolic, and/or Neurology
Bachelor's Degree Degree in scientific discipline or health care preferred
Benefits
Dependent on the position offered, incentive plans and/or bonuses may be offered.
Dependent on the position offered, a range of health and welfare and/or other benefits may be offered.
Glassdoor
3.9
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
Durham, North Carolina, USA
https://www.iqvia.com
Distribution of Different Job Fields Receiving Sponsorship
46
Represents job field similar to this job
Engineering and Development
Management and Executive
Sales
Customer Service and Support
Product Management
Education and Training
Marketing
Accounting and Finance
Creatives and Design
Arts and Entertainment
Trends of Total Sponsorships
*2026
(150)
2025
(163)
2024
(282)
2023
(255)
2022
Qualifications
Candidate are required to have 6 months to 2 years of onsite monitoring experience within oncology
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
Good therapeutic and protocol knowledge as provided in company training
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable)
Written and verbal communication skills including good command of English language
Organizational and problem-solving skills
Effective time and financial management skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Cardiovascular/Renal/Metabolic, and/or Neurology
Bachelor's Degree Degree in scientific discipline or health care preferred
Required skills
Oncology Clinical Research, Onsite Clinical Monitoring, Clinical Practice (GCP), International Conference on Harmonization (ICH) Guidelines, Clinical Research Protocol Knowledge, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Preferred skills
Cardiovascular/Renal/Metabolic, and/or Neurology
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