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5I
5PY IQVIA RDS Inc.
Regulatory Affairs Director
Career Insights for Regulatory Affairs Manager
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Based on North Carolina data
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What they do
A Regulatory Affairs Manager plans, directs, or coordinates production activities of an organization to ensure compliance with regulations and standard operating procedures.
$201,726 / year median in North Carolina
+1% projected growth
Job Description
Job Overview Direct, oversee and manage large, complex, regulatory projects, ensuring quality deliverables on time and within budget. Essential Functions
- May act as a Project Manager for a large and complex stand-alone project or programme, involving several regulatory or technical deliverables and/or region, and/or operations
- Undertakes risk analysis, management and contingency plans
- Must ensure that regulatory colleagues on the project have the tools and training needed to undertake the various tasks
- Provides strategic regulatory and/or technical consultancy on a variety of projects, internally and externally, using innovative solutions where appropriate to produce consistent results
- Ensures compliance of regulatory processes and prepares for full Regulatory Affairs Systems Audits, accountable for any subsequent action plans
- Competently manages meetings/expectations with Regulatory Agencies and/or groups within IQVIA
- May take leadership role in bid defense strategy and planning
- May act as global regulatory or technical representative in major cross-functional global initiatives and/or may lead a global regulatory/technical initiative
- May lead/chair a session on Regulatory Affairs or related topics at a conference; deliver effective presentations to a broad audience
- Responsible for making major improvements to processes and systems across functions or large departments
- Problems faced are highly complex and require solutions drawn from best practices and expertise, as well as from extensive analysis into the root cause Qualifications
- Bachelor's Degree Lifescience or related discipline Required
- At least 10 years relevant experience including 8 years regulatory experience
- Requires extensive knowledge of multiple job areas obtained through advanced education and experience; Viewed as a leading expert within the field by peers
- Extensive experience in regulatory and/or technical writing
- 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
- Strong software and computer skills, including Microsoft Office applications
- Acts as a role model to junior colleagues; possesses a positive attitude and communication style to customers and colleagues
- Communicates effectively with all levels of the organization and remains motivated and enthusiastic in times of change and other pressure situations
- 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.