Top 29 Director of science Jobs in Hampton Nj

Associate Director, Clinical Science
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $162,400 - $243,600 a year
- Office
- Master's degree
- Bachelor's degree
Associate Director, Consumer Safety Science
Haleon —Warren, NJ
- $156,313 - $214,930 a year
- Full-time
- Hybrid work
- Medicine
- 5 years
- Office
- Paid parental leave
- Health insurance
Head of Clinical Data Management
Insmed Incorporated —Bridgewater, NJ
- $255,000 - $347,500 a year
- Full-time
- Remote
- Computer Science
- Master's degree
- 8 years
- Employee stock purchase plan
- Disability insurance
Director, Data Management Process, Quality & Inspection Readiness
Regeneron —Warren, NJ
- $183,100 - $305,200 a year
- Office
- Bachelor's degree
- Travel
- Health insurance
- Dental insurance
Senior Director, Clinical Science
Celldex Therapeutics —Hampton, NJ
- $203,157 - $263,841 a year
- Business development
- Doctor of Philosophy
- Mentoring
- Paid holidays
- Health insurance
3d
Senior Director, Clinical Safety Scientist
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $242,700 - $404,500 a year
- 5 years
- Doctor of Philosophy
- Mentoring
Associate Director, Companion Diagnostics Leader
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $166,720 - $250,080 a year
- Bachelor of Science
- Analysis skills
- Bachelor's degree
8d
Associate Director, Biostatistics (Late Stage)
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $175,440 - $263,160 a year
- 5 years
- Office
- Master's degree
Senior Director, Global Health Economics Outcomes Research (HEOR)
PTC Therapeutics, Inc. —Warren, NJ
- $246,900 - $310,800 a year
- Full-time
- Medicine
- Doctor of Philosophy
- Children
- Dental insurance
- Vision insurance
Quick Apply
Director, Clinical Science
Celldex Therapeutics —Hampton, NJ
- $176,659 - $229,427 a year
- Analysis skills
- Continuous improvement
- Doctor of Philosophy
- Paid holidays
- Health insurance
3d
Director, Formulation Development
PTC Therapeutics, Inc. —Bridgewater, NJ
- $215,200 - $270,900 a year
- Full-time
- Master's degree
- 8 years
- Doctor of Philosophy
- Dental insurance
- Vision insurance
Quick Apply
Director, Project Management - Oncology
Precision Medicine Group —Gladstone, NJ
- $162,000 - $243,000 a year
- Online Application
- Remote
- Microsoft Excel
- Microsoft Outlook
- Business development
1d
Associate Director, Epidemiology Analytics
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $157,920 - $236,880 a year
- Master's degree
- SQL
- Analysis skills
Sr. Director, Epidemiology, Immunology - Hampton, NJ
Celldex Therapeutics —Hampton, NJ
- $203,157 - $263,841 a year
- 8 years
- Doctor of Philosophy
- Senior level
- Paid holidays
- Health insurance
3d
Head of Global Biostatistics
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $271,500 - $452,500 a year
- 6 years
- Math
- Doctor of Philosophy
Director, Pharmacovigilance / Product Safety
Insmed Incorporated —Bridgewater, NJ
- $247,000 - $337,000 a year
- Full-time
- Medicine
- Microsoft Excel
- Microsoft Outlook
- Employee stock purchase plan
- Disability insurance
Director, Clinical Data Management
PTC Therapeutics, Inc. —Warren, NJ
- $200,700 - $252,600 a year
- Full-time
- Hybrid work
- Java
- C++
- Supervising experience
- Dental insurance
- Vision insurance
Quick Apply
Director, Translational Bioanalytical Sciences
Insmed Incorporated —Bridgewater, NJ
- $185,000 - $252,500 a year
- Full-time
- Hybrid work
- Office
- Doctor of Philosophy
- Travel
- Employee stock purchase plan
- Disability insurance
2d
Associate Director, Regulatory Affairs
Insmed Incorporated —Bridgewater, NJ
- $164,000 - $213,000 a year
- Full-time
- Remote
- Microsoft Outlook
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
4d
Associate Director, Clinical Data Management
PTC Therapeutics, Inc. —Warren, NJ
- $163,800 - $206,200 a year
- Full-time
- Hybrid work
- Java
- 8 years
- C++
- Dental insurance
- Vision insurance
Quick Apply

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director of science jobs near hampton nj

Associate Director, Clinical Science

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

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Job Details

$162,400 - $243,600 a year

Qualifications

Bachelor's degree

Full Job Description

Job Title:
Associate Director, Clinical Science

Job Requisition ID:
1799

Posting Start Date:
7/13/26

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 more than 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.

Job Summary

Under supervision of Clinical Science Asset Lead or Clinical Science Lead within Hematology, drafts development plans, protocol profiles, protocols, informed consent forms, and sections of submission documents. Oversees a clinical trial. Prepares clinical section of regulatory document. Represents Clinical Science on Project Team and collaborates as team member with other functions, AROs/CROs. Provides scientific direction to Clinical Operations and other functions. This position requires minimal supervision to provide critical study-level support to the CSL/PS/MM/GCL for the successful execution of assigned studies.

Responsibilities

Study Strategy:
Under supervision of Clinical Science Asset Lead or Clinical Science Lead, drafts development plans.

Participates in the development of study design to meet study objectives by owning sections/components.

Provides strategic direction to Biostatistics and Data Operations (BDO) for EDC, edit checks, data quality listings, SAP, Data Mgmt plan and to Clinical Operations on SDV plan.

Develops biomarker/PK strategy in collaboration with Translational Medicine and Clinical Pharmacology (TMCP).

With Data Management, co-leads or provides input to the Integrated Data Review Plan process.

Study Planning and Execution:
Provides input on major milestones of trial, clinical trial plan and contingency planning.

Analyzes and updates management on potential risks to study deliverables.

Leads study team in authoring of protocol and responsible for ICF creation or provides input on ICF creation.

Consults and recruits members for DSMB and/or adjudication committee setup and develops supporting documents and charters.

Leads development of protocol deviation management plan and contributes to monitoring protocol compliance to ensure proper identification and categorization of protocol deviations.

Reviews inclusion/exclusion criteria and other study design elements for consistency with study strategy.

Oversees recruitment and retention; establishes and implements contingency plans for shortfalls.

Study outputs:
Reviews emerging clinical data regularly and shares data review findings with the study team.

Performs quality assessment with Delivery Lead e.g. review Tables/Listings/Graphs before database lock and quality check of data; works with BD&O to ensure SAP update.

Leads dose-escalation meetings and other site facing interactions with Clinical Operations.

Collaborates with Translational Medicine and Clinical Pharmacology to ensure appropriate biomarker, PK / PD measurements.

Draft clinical sections of regulatory documents and responses to IRBs and Health Authorities.

External collaboration:
Consults with internal experts and external KOLs, Ad Boards for protocol development.

Provides input on CRO / ARO Statement of Work and Budget; represents Clinical Science in study team meetings with CRO and ARO

Establishes effective communication between CRO / vendors / ARO.

Additional non-study related activities:
Occasional senior management interactions at FIHC, WDC.

Initiates contact w/KOL and prepares material for KOL interactions to support study-based needs.

Supports due diligence activities related to in-licensing and acquisitions.

Qualifications

Education Qualifications

Bachelor's Degree life sciences or related field required

Master's Degree, PharmD, or PhD preferred

Postgraduate training in TA or related specialty, or equivalent, preferred

Experience Qualifications

4+ years with PharmD, PhD and relevant clinical experience preferred

7+ years with Bachelor's or Master’s degree and relevant clinical experience preferred

Hematology experience is preferred

Advanced Technical Expertise: Possess advanced understanding of pre-clinical and clinical research, including protocol writing, data review, study design, and disease area knowledge preferred

Travel Requirements

In-house office position that may require travel (global, up to 30%).

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration 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.

Salary Range:
USD$162,400.00 - USD$243,600.00

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Refine Your Search

director of science jobs in hampton nj

Associate Director, Clinical Science

Associate Director, Consumer Safety Science

Head of Clinical Data Management

Director, Data Management Process, Quality & Inspection Readiness

Senior Director, Clinical Science

Senior Director, Clinical Safety Scientist

Associate Director, Companion Diagnostics Leader

Associate Director, Biostatistics (Late Stage)

Senior Director, Global Health Economics Outcomes Research (HEOR)

Director, Clinical Science

Director, Formulation Development

Director, Project Management - Oncology

Associate Director, Epidemiology Analytics

Sr. Director, Epidemiology, Immunology - Hampton, NJ

Head of Global Biostatistics

Director, Pharmacovigilance / Product Safety

Director, Clinical Data Management

Director, Translational Bioanalytical Sciences

Associate Director, Regulatory Affairs

Associate Director, Clinical Data Management

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