Director, Data Sciences, Safety and Regulatory, FSP Sales

DURHAM (US)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

Director, Data Sciences, Safety and Regulatory, FSP Sales

Director, Data Sciences, Safety and Regulatory, FSP Sales will contribute to a major segment of the Sales organization – FSP services for the Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions - and will be responsible for achieving FSP Sales targets from assigned portfolio of accounts.

Core responsibilities include

Achieving annual sales quota for assigned account portfolio, including individual quotas for each line of business.

Developing relationships with both IQVIA traditional customer base and non-traditional/new customers and markets, and actively prospecting new business opportunities for FSP services.

Establishing and executing a comprehensive sales plan for each target account. Monitor actions and results against plan.

Maintaining an advanced understanding of IQVIA’s specialized FSP offerings and providing “best practice” advice and solutions throughout sales cycle.

Cultivating relationships with key decision-makers within Account Teams and developing in-depth knowledge of the customers' organizations.

Identifying and responding to customer needs, defining potential opportunities, and proposing appropriate strategy/solution to customer.

Coordinating and overseeing the development of proposals and contracts for assigned accounts.

Maintaining customer, proposal, and contract tracking for assigned portfolio of accounts.

Managing customer inquiries and requests for information from both internal and external customers in a timely manner.

Developing and maintaining knowledge bank of IQVIA's position vs competitors in the FSP market, including positioning and pricing, specific reasons for awards and non-awards, duration of contractual engagements, and status.

Maintaining general knowledge of all IQVIA R&DS services for appropriate cross-sell opportunities and working across company's service lines and with sales teams to cross-promote and respond to RFPs as well as develop internal relationships needed to create solutions designed using multiple services.

Support sales and marketing services by attending, participating, and speaking at trade shows and industry conferences.

Skills and abilities

Must have direct experience with FSP delivery models, principles, pricing, and commercial terms.

Must have a proven track record with high-level customer contacts.

Must have excellent verbal, written, and presentation skills

Must act with a sense of urgency and be able to work both independently and within a team environment.

Must be Sales-driven, knowledgeable, consultative, a problem solver, customer focused, creative, resourceful, and fast-moving.

Requirements

Bachelor's Degree

12 years related experience, including 5 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or

Equivalent combination of education, training and experienceRequired

General knowledge of the Clinical Development space and Clinical Research Organization (CRO) operations are required.

Experience in the sales, contracting, and delivery of services in an FSP model.

Sales experience in a Clinical Research Organization, BPO, or Clinical Staffing Agency is required.

Operational experience in Clinical Data Management, Biostatistics, Statistical Programming, Medical Writing, Lifecycle Safety or Regulatory Affairs field is beneficial.

30% travel is required (based on location).

To be eligible for this position, you must reside in the same country where the job is located.

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  https://jobs.iqvia.com

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. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $111,200.00 - $309,800.00. 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.

REQUIRED VERIFIED SKILLS

Biostatistics
Regulatory Affairs
Medical Writing
Clinical Data Management
Clinical Research

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Director, Data Sciences, Safety and Regulatory, FSP Sales position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Clinical Data Associate ➔ Senior Data Manager ➔ Clinical Data Lead ➔ CDM Director.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: Biostatistics, Regulatory Affairs, Medical Writing. Prepare real-world examples demonstrating these skills for the interview.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.