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Job Title: Associate Director, Regulatory Affairs
Job Location: Indianapolis, Indiana, United States of America
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Job Overview
Line Management responsibilities for a team of Regulatory staff or may be responsible for the performance of one or more Regulatory Affairs sites. Responsible for the development of regulatory business, in accordance with Global Regulatory Affairs business plans. Participates in project-related work, as necessary.
Essential Functions
Manage staff in accordance with organization’s policies and applicable regulations; Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems; Approve actions on human resources matters, including salary administration;
Independently handles personnel issues, conflict management, defines goals that increase knowledge and skills of staff, and defines staff expectations, without involvement of senior managers;
Assists in the coordination of projects and resources, ensuring quality deliverables to customers;
May contribute to discussions on implementation of business strategy on a regional basis and will set and implement site-specific objectives, as appropriate; Ensures staff have a consistent understanding and positive impression of strategy for regional and global objectives;
May have financial responsibility and accountability for one or more Regulatory Affairs sites; Undertakes business development activities and monitors growth and performance, as required;
May undertake risk analysis and manages the outcome as appropriate;
Builds strong relationships with managers of other operations and acts as a positive ambassador for Regulatory Affairs;
May act as a Project Manager for a large stand-alone programme, involving several regulatory or technical deliverables and/or region, and/or operation; May provide strategic regulatory and/or technical consultancy on a variety of projects;
May manage meetings with Regulatory Agencies;
May write and/or review a complete single service regulatory proposal and defend costs and timelines to clients;
May plan and deliver workshops or presentations on Regulatory Affairs topics for conferences or publications;
Responsible for leading moderate to significant improvements of processes, systems or products to enhance performance of job area;
Problems faced are difficult and moderately complex, and require detailed information gathering, analysis and investigation to understand;
May be assigned as Reviewer and/or Approver for Regulatory standard operating porcedures or cross-functional standard operating porcedures owned by other operations;
May support global regulatory or technical initiatives or act as a regional representative on a cross-functional initiative;
Performs other duties, as business needs require;
Qualifications
Bachelor's Degree Degree in Lifescience or related discipline Req Or
Master's Degree Degree in Lifescience or related discipline
At least 6 years regulatory experience including 3 years management experience (or a combination of education, training and experience)
Possesses a specific regulatory or technical expertise;
Good, solid interpersonal communication (oral and written) and organization skills;
Strong software and computer skills, including Microsoft Office applications;
Demonstrates negotiation skills and is confident in making decisions with minimal supervision;
Ability to work on several projects, retaining quality and timelines;
Possess demonstrated working knowledge of corresponding professional grade level responsibilities, skills and abilities, as required for guidance of staff
Demonstrate success in leading teams or previous experience in a supervisory capacity;
Advanced negotiating and influencing skills and the ability to identify and resolve issues, using flexible adaptable approach. Remains calm, assertive and diplomatic in challenging interactions with customers;
Sets a positive example to staff, relating to professionalism, attitude and interaction with colleagues and customers;
Understands and promotes Corporate and Global Regulatory Affairs Business Unit strategies, communicating this in a positive manner to staff;
Ability to provide fair, timely, appropriate and constructive feedback and guidance to staff;
Ability to earn trust of staff, acting in confidence and with sensitivity when dealing with personnel issues, staff expectations and conflict management;
Demonstrates confidence and appropriate communication style in representing staff issues or concerns to senior management; Possess demonstrated working knowledge of corresponding professional grade level responsibilities, skills and abilities, as required for guidance of staff;
Line management experience required, with demonstrated success in staff development, engagement, and performance;
Ability to manage competing priorities, as appropriate;
Advanced negotiating and influencing skills and the ability to identify and resolve issues, using flexible adaptable approach, Remains calm, assertive and diplomatic in challenging interactions with staff and customers;
Sets a positive example to more junior staff relating to professionalism, positive attitude and communication style to customers and colleagues, Communicates effectively and confidently with various levels of the organization, as appropriate; remains motivated and enthusiastic in times of change and other pressure situations
Possess practical knowledge in leading and managing the execution of processes, projects and tactics within one department or multiple related departments;
Ability to exercise independent judgement taking calculated risks when making decisions;
Applicable certifications and licenses as required by country, state, and/or other regulatory bodies
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 $103,600.00 - $288,600.00. 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.
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