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59 Incyte Clinical Trial Manager Jobs Hiring Near You

Prior launch experience and clinical trial expertise preferred. * Experience in strategic planning ... Management reserves the right to change or modify such duties as required. Incyte Corporation is ...

New Product Planning

Chadds Ford, PA

$125.30K - $165.40K/yr

... to trial design/evidence generation, regulatory/labeling strategy, and differentiation vs. standard of care; translate scientific and clinical data into commercial implications, risks, and ...

New Product Planning

Chadds Ford, PA · On-site

$125.30K - $165.40K/yr

... to trial design/evidence generation, regulatory/labeling strategy, and differentiation vs. standard of care; translate scientific and clinical data into commercial implications, risks, and ...

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Incyte Jobs Information

What are the key skills and qualifications needed to thrive as a Clinical Trial Manager, and why are they important?

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What are some common challenges Clinical Trial Managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.

What does a Clinical Trial Manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.
What are the most popular categories at Incyte?
Infographic showing various Clinical Trial Manager job openings at Incyte in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 95% Physical, and 5% Remote job distribution.
Data Analytics Manager (Clinical)

Data Analytics Manager (Clinical)

Incyte Corporation

Chadds Ford, PA • Hybrid

Other

Posted 14 days ago


Job description

Overview

A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity

Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.

Data Analytics Manager (Clinical)

Reporting to the IT Director of Data Products and Analytics, the Data Analytics Manager will own the development and operation of data products aligned to Incyte's Clinical Development Operations and PMO functions. The data product portfolio consists of data pipelines, outbound integrations to external applications, data lakehouses, and reporting built in Microsoft Fabric + Power BI. The Data Analytics Manager will lead a primarily offshore (India & LATAM) technical team of 10-20 contract data engineers and data analysts. The ideal candidate has a blend of hands-on data analytics technical expertise, leadership ability, and clinical development operations domain expertise. The ideal candidate is comfortable working in a dynamic fast-paced environment and highly motivated to grow in responsibility. This position is hybrid with expectation to be in office 4 days per week in Chadds Ford PA and/or Wilmington, DE.

Responsibilities

* Accountable for data product delivery in a GxP-regulated environment using Microsoft Fabric / Power BI for Clinical Development Operations and PMO functions.

* Engage and manage business and IT stakeholders throughout the requirements gathering, delivery, and testing process. Negotiate project scope, cost, timeline, and changes.

* Design technical solutions based on business requirements in alignment with IT architecture standards and processes.

* Lead technical project delivery teams consisting of data / BI engineers including assigning work, tracking progress, and providing technical guidance.

* Work with clinical stakeholders to define data strategy including overall architecture, data governance, and KPIs.

Required Skills & Experience

* Excellent communication and stakeholder management skills. Must be able to effectively explain complex technical information to non-technical stakeholders.

* Demonstrated ability to design and govern enterprise-scale lakehouse architectures (e.g., medallion pattern, dimensional modeling, RBAC, data lineage, performance optimization) in Microsoft Fabric or comparable cloud platforms.

* Experience with managing complex projects with tight deadlines, budget constraints, and dependencies across multiple teams.

* Experience managing distributed global teams across time zones including vendor management, contract oversight, code review, capacity planning, and performance management.

* Experience with relevant life sciences clinical data systems / providers (CTMS, EDC, CROs) and analytics related to risk based quality management (RBQM), operational trial performance, study startup, and site performance monitoring.

* Experience with GxP in a data engineering & analytics context including computer system validation, data integrity, supporting audits, and 21 CFR Part 11

* 10+ years of experience related to the above requirements in roles with increasing responsibility.

Preferred Experience

* Direct experience with Veeva Development Cloud (CTMS, CDB, eTMF, OpenData, etc), Planisware, CRO data (IQVIA, ICON, etc), and other Clinical Development related data systems/providers.

* Hands-on technical expertise with the following data platform technologies: Microsoft Fabric, Databricks, PySpark, and/or Power BI.

* Hands-on experience with the following developer tools / practices: Azure DevOps, GitHub, CI/CD, AI-assisted code generation (e.g. Cursor, GitHub CoPilot, Claude Code, etc)

* Prior people management experience

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

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Learn more at: http://www.incyte.com/privacy-policy

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