IQVIA · 20 hours ago
Senior Research Scientist
Durham, North Carolina, United States of America
Full-time
Onsite
Mid, Senior Level
$77K/yr - $161K/yr
3+ years expIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Senior Research Scientist will provide medical, clinical and scientific advisory expertise, monitor clinical trials, and collaborate with various teams to ensure compliance with protocols and regulatory requirements.
AnalyticsHealth CareLife Science
Responsibilities
Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements
Review and evaluate clinical data in the generation of study concepts and protocols in the relevant therapeutic area and maintaining a high level of awareness of scientific developments and the competitive environment to assist on ongoing strategic re-evaluation of the program
Work closely with the Clinical Operations, Clinical Sciences and Global functional teams to ensure the translation of the protocol and clinical development plans into executable operational processes
Lead internal or external training as required and support the medical monitor in responses to investigators and other site personnel regarding clinical and study conduct questions
Independently review study subject level data for presentation to the medical monitor for clinical decision making, throughout the study life cycle. Liaises closely with the clinical safety scientist to support ongoing aggregate safety data review during a given clinical study
May manage alone or in collaboration with clinical safety the operational functioning of data monitoring committees and/or clinical adjudication committees. Clinical Scientist may participate in and present at these meetings, as required
Participate in analyzing and interpreting data from clinical studies, and writing/editing or reviewing results in study reports, regulatory submissions, abstracts, posters, presentations, peer reviewed manuscripts, and other documents. As required, lead internal data review meetings to determine strategic interpretation
May become a member of the company publication group. Additionally serve as a scientific reviewer for company publications and external research proposals in the area(s) of expertise
Participate in the Clinical Operations and Clinical Development teams. Provide support to the clinical development team (CDT) through meeting management support and communication. Act as the delegate or lead where required
Interact with internal auditing groups on a study level to ensure clinical development activities are conducted according to internal SOPs and work practices and in compliance with ICH-GCP
Qualification
Required
Bachelor's Degree or equivalent experience
3-5 Years of relevant industry experience
Excellent communication (interpersonal, verbal and written) skills, ability to communicate effectively at all levels
Knowledge of PC applications
Ability to work with global teams
Ability to travel
Knowledge of Health/Safety and Environment good practice
Duty to comply with all applicable standards as required by the company
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
10001+ employees
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (294)
2023 (261)
2022 (229)
2021 (208)
2020 (180)
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
Recent News
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