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

• Bachelor's 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.

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 $82,600.00 - $229,900.00. 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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