Sr. Dir, Product Offering, MedTech Quality, Regulatory, Safety & Compliance

IQVIA MedTech provides solutions and services dedicated to supporting the needs of the medical device and in vitro diagnostics industry from Concept to Patient.

Position Overview:

Align IQVIA MedTech sales consulting product management and marketing around a common growth strategy to expand the customer base and strengthen executive relationships with Quality Regulatory and Compliance professionals within the MedTech & IVD industry.

Essential Functions and Responsibilities:

• Partner with key IQVIA stakeholders and external leaders to develop competitive differentiated and relevant technology and consulting offerings for the QARA and Compliance functions.
• Expand C-suite and QARA functional leadership engagement within priority accounts strengthen strategic relationships and increase influence with Quality Regulatory and Safety decision makers.
• Lead the adoption of integrated solutions selling strategies across technology consulting and services offerings to increase share of wallet and deliver greater customer value.
• Develop marketplace analysis that monitors trends and helps quantify the most promising opportunity areas.
• Maintain an advanced technical and commercial understanding of Quality Regulatory and Safety technologies and services offerings and provide best practice advice throughout the sales cycle.
• Drive the development and execution of marketing and promotional plans.
• Build relationships with internal stakeholders create in-depth strategy presentations and define and drive the execution of implementation plans.
• Actively participate in proposal preparation meetings and/or proposal defense meetings as needed.
• Manage staff in accordance with organizations policies and applicable regulations.

Requirements & Qualifications:

• To be eligible for this position you must reside in the same country where the job is located.
• US remote with ability to travel approximately 20%.
• Bachelors Degree Required.
• 15 years relevant experience in Quality Regulatory Safety or Commercial Compliance within the MedTech industry or agency environment with 4 years management experience Required.
• Exceptional leadership presentation communication and influencing skills
• Demonstrated experience in managing global teams in a matrixed multi-regional organization delivering global initiatives
• Strategic business awareness of Medical Device and/or IVD industry and the ability to translate emerging industry trends relevant to the organization.
• Ability to work creatively in a fast-paced environment maintaining flexibility and changing priorities to meeting demanding timelines.
• Strong team player with high level of stress tolerance.
• Strong financial analytical and problem-solving skills with the ability to develop and articulate recommendations and solutions based on this analysis.
• Strong organizational planning project management and logistics skills.
• Strong software and computer skills including MS Office applications.

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.