招聘
Job Overview Manage and lead activities associated with Feasibility and/or Site Identification for regional and/or country projects and/or programs.
Essential Functions
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Manage assigned opportunities/projects/programs for country or region and adhere to timelines and budget.
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Ensure the site list for assigned studies includes an adequate number of appropriate investigators in accordance with the needs of the sponsor and specificataions of the protocol.
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Collect and analyze country/regional Feasibility and/or Site Identification information to meet timelines of each study.
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Attend kick off meetigs to understand study requirements include investigator profile, protocol, process speoifics and timelines.
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Raise questions and make suggestions based on SID SOPs and Work Instructions.
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Distribute, track, negotiate and review the Condidential Disclosure Agreements (CDAs) for Feasibility and/or Site Identification with input from the study team, management and Legal when appropriate.
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Distribute, track and review Site Questionnaires for Feasibility and/or Site Information Forms or Site Qualification Questionnaires for SID
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Ensure completeness, site capability and suitability fo the study.
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For SID review SIF and/or SQQ vs the guidance document and approve for SSV or select appropriate sites.
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Manage investigator database entry and quality, ensuring complete investigator and site information is captured and monitor for duplicate entries.
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Maintain and update company information repositories and databases.
Qualifications
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Bachelor’s degree in Life Sciences, or a related field
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1-2 years clinical research experience on Feasibility and/or Site Identification ready to enroll activities. Equivalent combination of education, training and experience.
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 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.
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About IQVIA

IQVIA
PublicFocused on health information technology and clinical research.
10,001+
Employees
Durham
Headquarters
$17B
Valuation
Reviews
3.9
2 reviews
Work Life Balance
2.5
Compensation
2.0
Culture
2.8
Career
3.0
Management
2.5
65%
Recommend to a Friend
Pros
Structured feedback and development process
Meaningful contribution to client businesses
Problem-solving with specialized knowledge
Cons
Strict performance requirements and termination risk
High-level rubric definitions lack detail
No performance bonuses offered
Salary Ranges
42 data points
Mid/L4
Director
Mid/L4 · Client Operations Lead
2 reports
$102,928
total / year
Base
$89,416
Stock
-
Bonus
-
$101,093
$104,664
Interview Experience
3 interviews
Difficulty
3.0
/ 5
Duration
14-28 weeks
Experience
Positive 0%
Neutral 33%
Negative 67%
Interview Process
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Manager Interview
5
Executive/GM Interview
6
Offer
Common Questions
Behavioral/STAR
Case Study
Technical Knowledge
Past Experience
Culture Fit
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