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  1. Home
  2. chevron_right
  3. scientific & qa
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  5. Dir Clinical Operations Non-MD
Daiichi Sankyo US logo

Dir Clinical Operations Non-MD

Not Disclosed•Full-TimeOn-site

location_on316, Lyons Road, Liberty Corner, Bernards Township, Somerset County, New Jersey, 07920, United States

Apply Now

About Daiichi Sankyo

At Daiichi Sankyo, we are united by a single purpose: to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and over 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society," we are shaping a healthier, more hopeful future for patients, their families, and society.

About the Role

This Director-level position provides operational oversight to study management personnel within assigned programs, serving as a critical extension of the Senior Director, Clinical Operations. The role exists to ensure that study deliverables are met, risks are identified and mitigated, and data-driven strategies are implemented to keep programs on track.

In this capacity, you will act as a Subject Matter Expert (SME) on study management processes, fostering the growth and credibility of the Global Clinical Operations (GCO) organization. You will work closely with the Asset Lead to share lessons learned and best practices, while also representing operations at Global Project Team (GPT) meetings to support larger program goals. A key part of your day involves mentoring direct reports, ensuring they are properly trained on Standard Operating Procedures (SOPs), and driving continuous improvements in GCO quality and metrics.

Hiring Process

Qualified candidates will be considered for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Equal Opportunity

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. We are committed to building a diverse and inclusive workforce that reflects the communities we serve.

Work location

Work model: On-site

location_on

316, Lyons Road, Liberty Corner, Bernards Township, Somerset County, New Jersey, 07920, United States

Bernards Township, New Jersey

Key Responsibilities

  • check_circleProvide operational oversight to study management personnel and ensure delivery of study milestones
  • check_circleDevelop talent through career development, performance management, and mentoring of direct reports
  • check_circleDesign, update, and implement innovative procedures and SOPs for clinical study oversight and execution
  • check_circleAnalyze study metrics and risks to implement strategies and course corrections for assigned programs
  • check_circleRepresent Global Clinical Operations on strategy teams and collaborate with stakeholders to align goals
  • check_circleReview resources against the development pipeline to identify gaps and ensure adequate staffing levels
  • check_circleManage CRO and vendor relationships to ensure compliance with quality measures and performance standards

Requirements

  • verifiedBachelor's Degree in the Sciences
  • verified10 or More Years relevant experience
  • verified4 or More Years with a MS/MPH preferred
  • verified4 or More Years with PharmD/PhD preferred
  • verifiedCRA experience preferred
  • verifiedAbility to travel up to 20% of the time

Nice to Have

Master of Science (MS) or Master of Public Health (MPH) degree. PharmD or PhD degree. Clinical Research Associate (CRA) experience. Time spent directly in a medical environment (e.g., as a Study Site Coordinator).

Daiichi Sankyo US logo
Company

Daiichi Sankyo US

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

10+ yrs (Lead)

Education

Bachelor's Degree in the Sciences preferred

Job Type

Full-Time

Skills Required

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Skills, education and keywords

Skills: Clinical Study Oversight, Sops, CCSR, CDP, Protocols, Study Management, Global Clinical Operations, Cra, Study Site Coordinator, Pharmaceutical Company.

Education: Bachelor's Degree in the Sciences preferred; PharmD/PhD preferred.

Frequently asked questions about Dir Clinical Operations Non-MD at Daiichi Sankyo US

What does a Dir Clinical Operations Non-MD at Daiichi Sankyo US do?expand_more
A Dir Clinical Operations Non-MD at Daiichi Sankyo US is responsible for the following: Provide operational oversight to study management personnel and ensure delivery of study milestones; Develop talent through career development, performance management, and mentoring of direct reports; Design, update, and implement innovative procedures and SOPs for clinical study oversight and execution; and Analyze study metrics and risks to implement strategies and course corrections for assigned programs.
What are the requirements for this Dir Clinical Operations Non-MD role?expand_more
To qualify for the Dir Clinical Operations Non-MD at Daiichi Sankyo US position, applicants should have: Bachelor's Degree in the Sciences; 10 or More Years relevant experience; 4 or More Years with a MS/MPH preferred; 4 or More Years with PharmD/PhD preferred; CRA experience preferred; and Ability to travel up to 20% of the time.
Where is the Dir Clinical Operations Non-MD role at Daiichi Sankyo US located?expand_more
Dir Clinical Operations Non-MD at Daiichi Sankyo US is based in 316, Lyons Road, Liberty Corner, Bernards Township, Somerset County, New Jersey, 07920, United States. This is a on-site role.
Is this Dir Clinical Operations Non-MD job remote, hybrid, or on-site?expand_more
Daiichi Sankyo US has listed this Dir Clinical Operations Non-MD role as on-site.
How much experience is required for this Dir Clinical Operations Non-MD role?expand_more
Dir Clinical Operations Non-MD at Daiichi Sankyo US typically requires 10+ years of relevant experience at the lead level.
What skills do you need for the Dir Clinical Operations Non-MD role at Daiichi Sankyo US?expand_more
Key skills for Dir Clinical Operations Non-MD at Daiichi Sankyo US include Clinical Study Oversight; Sops; CCSR; CDP; Protocols; Study Management; Global Clinical Operations; and Cra.
What education is required for Dir Clinical Operations Non-MD at Daiichi Sankyo US?expand_more
Educational requirements for this role: Bachelor's Degree in the Sciences preferred; and PharmD/PhD preferred.
What category does the Dir Clinical Operations Non-MD role belong to?expand_more
Dir Clinical Operations Non-MD at Daiichi Sankyo US is part of the scientific & qa job category on Recrutus.
Recrutus

Curating the world's most innovative career opportunities. We bridge the gap between visionary talent and industry-leading companies.

Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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Browse jobsCompanies hiringRemote jobsJobs by locationJobs by cityJobs by categoryJobs by skillCareer guidesCareer blogSalary insights
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Recrutus helps candidates discover roles that match their skills and helps teams reach qualified applicants faster. Browse by metro, discipline, or work style — from internships to senior leadership.

© 2026 Recrutus. All rights reserved.
Terms of serviceCookie policyAcceptable useDMCA policyEmployer termsCandidate terms
Clinical Study OversightSopsCCSRCDPProtocolsStudy ManagementGlobal Clinical OperationsCraStudy Site CoordinatorPharmaceutical Company
US privacy notice
Accessibility