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Study Delivery Lead

Job in Bernards Township, Somerset County, New Jersey, USA
Listing for: Daiichi Sankyo
Full Time position
Listed on 2026-01-01
Job specializations:
  • Healthcare
    Healthcare Management
  • Management
    Healthcare Management, Data Science Manager
Salary/Wage Range or Industry Benchmark: 168000 - 252000 USD Yearly USD 168000.00 252000.00 YEAR
Job Description & How to Apply Below

Join a Legacy of Innovation 125 Years and Counting!

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world‑class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people.

In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.

Summary

The Study Delivery Lead (SDL) leads the cross‑functional core and extended clinical study team in end‑to‑end delivery of the clinical trial with consistency, quality and per planned timelines. The SDL has the accountability for one or several complex studies in various settings including Phase I‑III, within a delivery model comprising outsourced studies or outsourced studies with elements of in sourcing. This includes global operational execution and delivery of clinical studies across multiple geographic regions, in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Health Authority regulations, International Conference on Harmonization (ICH) guidelines and local regulations, as required.

The SDL is accountable for operational planning and execution at the study level with responsibility for clinical study plans and execution (from planning start‑up, conduct, reporting and close‑out) including timeline and budget. The SDL will partner with the Strategic Vendor Oversight (SVO) team and collaborate with the core and extended team to ensure robust CRO oversight including third‑party vendors to achieve study milestones and deliverables according to agreed quality standards and timelines and that quality of data is suitable for regulatory submission.

The SDL collaborates with cross‑functional stakeholders and the Metrics, Analytics, Reporting and Solutions (MARS) team to drive and monitor progress. The SDL fosters an environment where the core study team maximizes their expertise and contribution to trial delivery, including but not limited to issue resolution, risk mitigation and escalation to the Global Project Team (GPT), SCORE and other governance levels as needed.

The SDL will have regular interactions with key internal and external stakeholders to discuss project status, elevate issues, and troubleshoot inquiries. For this role, strong written and verbal communication skills in English, operational leadership, decision‑making, the ability to delegate, strategic thinking, conflict resolution, clinical project management experience and attention to detail are required. The SDL is an experience matrix leader and serves as a mentor to more junior colleagues on clinical trial execution.

Outside interfaces may include other Daiichi‑Sankyo business groups and subsidiaries in the US and abroad, governmental, academic, community and industry organizations. The SDL is the reference and role model within the study delivery lead team that drives the culture for a healthy team. The role is primarily responsible for operational study strategy and study execution while exhibiting leadership qualities.

Responsibilities
  • Lead the core study team while project managing and collaborating with internal stakeholders to ensure cross‑functional integration and delivery of study milestones (e.g., protocol, eCRF/EDC, IXRS, Clinical Study Oversight Plan)
  • Ensure operational study‑level timeline, budget, deliverables and quality management
  • Facilitate escalation and resolution of issues with CRO/vendors/site/country performance raised by the study team, including serious quality incidents and serious breaches of GCP. The SDL is accountable for escalation to the OPL/Asset Lead or Senior Line…
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