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Open nowPosted today

RWE Senior Site Strategy Lead

IQVIA1,848 open roles

Pay
$93,100 – $232,800 a year
Where
Durham, North Carolina, United States of America
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Your applicationOpen nowRWE Senior Site Strategy LeadIQVIA · Durham, North Carolina, United States of America

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The clock on this job

Early applications get read.

13.9% of postings close within 7 days. Measured by our own scanner across the market. IQVIA postings stay open a median of 29 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 13.9%7 days
  4. 22.4%14 days
  5. 38.1%30 days
  6. 59.0%60 days
This job: posted today

IQVIA median: 29 days open

The posting

Job Overview

The Site Strategy Lead (SSL) is integral to the development of our delivery strategies at the very early phase of proposal development, and is a key player in supporting the study specific requests for the Data Generation group from the clients in the request for proposal.

The SSL is key in building the most efficient and effective scenario for study execution during our sales process. This global team is working closely with other functional unit leads, and having the ability to build a strong proposal that IQVIA is able to operationalize and execute.

In addition to the pre-award support the team provides, the SSL is very involved in the post award phase early on, and will work with the assigned Clinical Operations Lead (COL) to ensure that the sold Data Generation strategy is passed on to the assigned study team.

Key Activities

  • Assist with overall project efficiency and adherence to project timelines and financial goals.
  • Assist with turning a study budget and strategy into action that make RWE studies more predictable, shorten timelines, improve data quality and provide innovative solutions to the clients.
  • Act as a single functional lead for Data Generation proposals, covering Site ID, Site and Patient Engagement, Site Management and Technology strategies.
  • Partners with internal teams to understand relevant challenges within a study and to identify the Data Generation strategies that can help meet these challenges.
  • Serves as single point of contact on the study to answer pre and post award site strategy questions.

Qualifications

  • Prior experience and knowledge of clinical operations – monitoring processes, documentation, GCP standards
  • In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Knowledge of project budgets and the use of pricing tools.
  • Strong analytical skills with ability to dissect budgets, negotiate prices with internal teams and understand the “big budget picture”.
  • Strong verbal and written communication skills
  • Results-driven with focus on excellence and quality.
  • Excellent time management skills, ability to manage several projects with overlapping deliverables & schedule.
  • Strong team player and collaborator with ability to operate in fast-paced environment.

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

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 $93,100.00 - $232,800.00. 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.

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