286 matching jobs for “Safety Data Lead I”

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Coupang

Area Manager (Taichung)

Taichung, Taiwan

Full time (company default)

Lead and Scale Regional Operations: Oversee day-to-day fulfillment and logistics operations across your …

Added Oct 4, 2026

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KLA

Senior Electrical Systems Engineer

Allentown, Pennsylvania, United States

Full time
Regular

Pay posted by employer$100,100–$146,833 per year

… including advanced etch and deposition systems. This role combines electrical system design, product safety, regulatory compliance, sustaining engineering, and new product development. The ideal candidate is a …

Added Oct 15, 2026

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Thermo Fisher Scientific

Medical Director - Principal Investigator

Prague, Czechia

… on – now and in the future. Day to day responsibilities: The Medical Director of our Integrated Phase I - IV clinic serves as a Principal Investigator and senior medical authority for the clinic, providing …

Added Oct 16, 2026

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Caterpillar

Autonomy Engineering Integration Specialist

Irving, Texas, United States

Pay posted by employer$128,470–$208,770

… enjoy living in it. This role contributes to the design, integration, validation, and delivery of Driver Safety System capabilities at Caterpillar. The Integration Engineer leads system-level integration activities that …

Added Oct 27, 2026

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Carrier Global

Director, HR Technology & AI Solutions

POL2789: Bobrowiecka 1, Warszawa, 00-728, Poland

The Director, HR Technology & AI Solutions position is a newly created leadership role designed to lead Carrier's HR AI transformation journey. You will develop and execute a multi-year workforce technology …

Added Oct 27, 2026

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Bristol-Myers Squibb

Director, Global Clinical Physician - Early HOCT

Cambridge Crossing - MA - US

Full time
Regular

Pay posted by employer$308,700–$374,075

… a primary source of medical accountability and oversight for multiple clinical trials · Manages Phase I/II studies, with demonstrated decision making capabilities, · Provides medical and scientific …

Added Oct 18, 2026

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Gilead Sciences

Assoc Clinical Development Director

Shanghai, China

Full time
Regular

… a clinical perspective. External Environment Assessment Maintain deep understanding of emerging clinical data, competitive intelligence, treatment guidelines, and evolving regulatory expectations in China. Establish …

Added Oct 15, 2026

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Thermo Fisher Scientific

Supervisor, Kit Production

Vilvoorde, Belgium

… the environment, making sure our food is safe or helping find cures for cancer. Position Overview: Lead and develop a high-performing manufacturing team to execute production schedules with precision, uphold …

Added Oct 16, 2026

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Thermo Fisher Scientific

Clinical Research Nurse II (Flexible Day Hours)

Prague, Czechia

… involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during …

Added Oct 16, 2026

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Thermo Fisher Scientific

Clinical Research Nurse

Prague, Czechia

Added Oct 16, 2026

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Bristol-Myers Squibb

Senior Pharmacovigilance Associate

Warsaw - PL

Full time
Regular

… stakeholders to provide strategic and operational support across therapeutic areas for signal detection, safety data review, safety management teams, and risk management. The position involves dedicated scientific and …

Added Oct 15, 2026

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Thermo Fisher Scientific

Qualified Person - PV, EU

Remote, Bulgaria +8 locations

… 2001/83/EC, associated EU regulatory guidance and applicable CRG procedures. Contributes to scientific safety services, such as safety writing, signal detection and/or literature surveillance. Oversees and supports …

Added Oct 16, 2026

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Coupang

Catalog Manager

Taipei, Taiwan

Full time (company default)

Strategic Leadership & People Management Team of Teams Leadership: Directly lead, mentor, and scale a multi-tiered organization, managing Assistant Managers and frontline auditors to …

Added Oct 14, 2026

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Merck (MSD)

Reliability Engineer Intern

SGP - Singapore - Singapore (70 Tuas West Dr)

… reduce repeat failures, and optimize lifecycle cost. Drive systematic defect elimination by providing data analysis on failure modes of recurring equipment issues. Track reliability KPIs (e.g., unplanned downtime, …

Added Oct 16, 2026

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IQVIA Holdings

Senior Statistical Programmer - FSP

Nairobi, Kenya +10 locations

and Accountabilities: Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, …

Added Oct 15, 2026

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Boeing

Senior Seat Systems Software Certification Engineer

GBR - Bristol, UK

Hybrid
Full time
Regular

… our suppliers and global Boeing sites. You will ensure our aircraft not only meets but exceeds the rigorous safety standards set forth by the European Aviation Safety Agency (EASA) and/or US Federal Aviation Authority …

Added Oct 14, 2026

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Coupang

Sortation Manager

Taoyuan, Taiwan

Full time (company default)

… labor plan for sort associates. Manages shift schedules, time-off requests, and performance coaching. * Safety & Quality: Maintains a safe working environment on the dock and sort floor. Oversees quality checks to …

Added Oct 4, 2026

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Coupang

Assistant Manager, Sortation Management

Taoyuan, Taiwan

Full time (company default)

… labor plan for sort associates. Manages shift schedules, time-off requests, and performance coaching. Safety & Quality: Maintains a safe working environment on the dock and sort floor. Oversees quality checks to …

Added Oct 4, 2026

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Thermo Fisher Scientific

AVI Software, Vision and Automation Systems Engineer

Greenville, North Carolina, United States

… configurations, recipes, control logic, and technical specifications. • Analyze inspection results, image data, and equipment behavior to improve accuracy, reliability, and operational performance; lead or support …

Added Oct 16, 2026

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Thermo Fisher Scientific

Senior Scientist, Biopharma - Athlone

Athlone, Ireland

… and testing oversight, owns non-routine technical deliverables within defined scope, and mentors Scientist I and II staff to ensure high-quality, consistent laboratory performance. This role serves as a senior …

Added Oct 25, 2026

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IQVIA Holdings

Senior Statistical Programmer - FSP

Nairobi, Kenya +10 more

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Experience · employer excerpt

• At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment• Indepth understanding of clinical programming and/or statistical programming processes and…
• Good experience in R Programming is mandatory for this role (Hands on experience)
• Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM).• Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent).• Proven…
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…
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,…

About this opportunity

Original employer description

The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.

Main Responsibilities and Accountabilities:

Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.
Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO.
Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.
Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables.

Additional tasks:

• Collaborates with CR&D staff regarding data analysis requests.
• Performs additional statistical analyses including but not limited to:
o support responses to regulatory agencies,
o generate integrated summary of safety and efficacy,
o support publications and presentations,
o support planning and reporting of clinical trials via exploratory analyses of available data,

Position Qualifications and Experience Requirements:

Education

• BSc in Computer Science, Mathematics, Statistics or related area with relevant experience

Experience

• At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment
• Indepth understanding of clinical programming and/or statistical programming processes and standards.
• Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills.

• Good experience in R Programming is mandatory for this role (Hands on experience)

• Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM).
• Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent).
• Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines.
• Experience in working in cross-functional, multicultural and international clinical trial teams.

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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