Associate Director Regional Clinical Operations (Oncology- Southeast)

Job Overview
Direct and manage project(s) and/or multi-project programs ensuring the quality of deliverables are on time and within budget. Ensure that all project work is completed in accordance with SOPs policies and practices.

Essential Functions
Manage the scope of work objectives timelines quality of deliverables and all other project management activities for the project(s) and/or multi-project program(s).
Serve as primary project contact with internal and external customers to ensure appropriate communication channels are maintained and reporting schedules adhered to.
Develop project plans for all phases of the project and associated deliverables.
Review project budget and scope of work including management of project budget(s) to meet financial and company goals proactively ensure adherence to change control processes.
Supervise maintenance of project management information and data tracking systems.
May direct project activities for team members regarding their project-oriented tasks to ensure that project milestones are met.
Evaluate impact of risks develop and implement quality and risk management plans for minimizing impact on project objectives and deliverables.
Continually review and ensure adequate internal and external resources are available to meet project deliverables and milestones.
Develop and implement continuous improvement processes for assigned projects.
Participate in RFP development and sales/proposal presentations; provides input on scope and budget development.
Provide technical expertise and project management experience to Project Manager(s) and training efforts.
Serve as a project management liaison with other groups within IQVIA.

Qualifications

Bachelors Degree minimum
7 years experience in Clinical Trial Operations including at least 3 years in a role of primary responsibility for clinical trial execution and management
Deep U.S. institutional engagement experience
Proven ability to build and sustain relationships with operational leaders and high-performing investigators and within key academic centers community sites with a track record of translating those relationships into strong enrollment outcomes.

Strategic partnership with Medical Science Liaisons
Experience working closely with MSLs to engage investigators inform site selection and strengthen overall site strategy. Candidates should be able to articulate how Clinical and Medical Affairs collaboration has enhanced site performance and enrollment and the distinct remits of each role.

Strength in site strategy and feasibility
Ability to proactively identify and prioritize the right sites using data institutional knowledge and field insights (including MSL input) and to continuously optimize the site mix based on performance.

Ownership of U.S. enrollment performance
Demonstrated success driving enrollment through thoughtful site engagement patient access strategies and targeted institutional partnerships including attention to diverse patient populations. Operates at a portfolio and strategy level not task execution

Country-level strategic thinking within global trials
Experience translating global study strategies into effective U.S. execution while serving as the voice of U.S. sites and investigators to global teams.

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. 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.