Clinical Research Site Manager, On-Site, Kansas City, MO
Clinical Research Site Manager, On-Site, Kansas City, MO
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$ 62400 - 156000
1 Vacancy
Job Description
Lead Clinical Trial Operations at Our Kansas City Site!
This is a fully on site leadership position within the Avacare site network group. Join Avacares dynamic and mission-driven team in Kansas City MO as a Site this leadership role youll drive clinical trial success through strategic oversight operational excellence and team development. Be a key contributor to advancing medical research and achieving organizational goals.
Overview
As Site Manager you will oversee the daily operations of our clinical research site ensuring studies are conducted in compliance with regulatory guidelines and internal standards. Youll lead a high-performing team collaborate cross-functionally and play a pivotal role in study execution across multiple therapeutic areas.
Essential Functions
Lead and manage site operations including staff training and development
Partner with Business Development to evaluate and place new studies
Develop and implement patient recruitment strategies to ensure enrollment success
Oversee multiple concurrent studies across various therapeutic areas
Conduct regular 1:1 meetings and annual performance reviews
Perform quality control checks and collaborate with Quality Assurance
Manage scheduling and coordination of patient/research participant activities
Ensure accurate source documentation data entry and query resolution
Support collection and review of essential study documents
Maintain compliance with study protocols GCP/ICH and regulatory requirements
Obtain informed consent and ensure participant safety and well-being
Facilitate site qualification initiation monitoring and close-out visits
Ensure proper handling and processing of laboratory specimens
Participate in leadership and management training programs
Qualifications
Hands-on clinical experience including obtaining vitals performing blood draws EKGs etc.
Associate Degree or higher preferred
Proven success as a lead Clinical Research Coordinator (CRC) with experience managing concurrent studies
Demonstrated ability to fulfill responsibilities equivalent to a CRC II or higher
Extensive knowledge of GCP/ICH guidelines and clinical trial regulations
Strong understanding of site operations and the drug development lifecycle
Experience in leadership project management and process improvement
Skilled in onboarding and training new team members including Research Assistants and CRCs
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
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. potential base pay range for this role when annualized is $62400.00 - $156000.00. 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.
Required Experience:
Manager
Employment Type
Full-Time
