Top 277 Associate director pharmaceutical Jobs in New Jersey

Associate Director, Biostatistics (Late Stage)
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $175,440 - $263,160 a year
- 5 years
- Office
- Master's degree
Director, Clinical Operations - AAV
Rocket Pharmaceuticals —Cranbury, NJ
- $196,000 - $294,000 a year
- Full-time
- Microsoft Outlook
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
8d
Associate Director Access & Reimbursement
CSL Seqirus —Summit, NJ
- $210,000 - $250,000 a year
- Full-time
- Bachelor's degree
- Contracts
- Budgeting
Production Operator
Biocon Biologics Limited —Cranbury, NJ
- $20 - $28 an hour
- Full-time
- OSHA
- English
- Mid-level
- Health insurance
- Dental insurance
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Associate Director, Heplisav B
Sanofi EU —Morristown, NJ
- $148,500 - $214,500 a year
- Hybrid work
- 5 years
- Bachelor's degree
- Neurology
- Parental leave
Associate Director, Statistical Programming
Everest Clinical Research —Bridgewater, NJ
- $170,000 - $205,000 a year
- Remote
- Computer Science
- 11+ years
- Databases
- AD&D insurance
- Disability insurance
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13d
Associate Director, US Brand Marketing
CSL Seqirus —Summit, NJ
- $180,000 - $205,000 a year
- Full-time
- 7 years
- Marketing
- Analysis skills
Associate Director Biostatistics
Penfield Search Partners —Princeton, NJ
- $185,000 a year
- Hybrid work
- 5 years
- Office
- Continuous improvement
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Associate Director, P2P Marketing
Novartis —East Hanover, NJ
- $152,600 - $283,400 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Travel
- Health insurance
- 401(k) matching
Senior Scientist, Viral Vector Process Development - Downstream
Rocket Pharmaceuticals —Cranbury, NJ
- $118,000 - $158,000 a year
- Full-time
- Microsoft PowerPoint
- Microsoft Word
- 6 years
- Paid holidays
- Health insurance
1d
Associate Director, Data Science - Market Access
Sanofi EU —Morristown, NJ
- $148,500 - $214,500 a year
- 5 years
- Bachelor of Science
- Office
- Parental leave
Associate Director, Precision Medicine
Bristol-Myers Squibb —Princeton, NJ
- $186,110 - $259,344 a year
- Email
- Hybrid work
- 3 years
- Doctor of Philosophy
- Travel
- Paid holidays
- Disability insurance
Associate Director, Global Medical Cardiovascular, Mavacamten
Bristol-Myers Squibb —Princeton, NJ
- $166,350 - $201,571 a year
- Email
- Hybrid work
- Medicine
- 5 years
- Doctor of Philosophy
- Paid holidays
- Disability insurance
Associate Director, Real World Evidence (RWE) Analytics
Sanofi —Morristown, NJ
- $148,500 - $214,500 a year
- Remote
- Bachelor of Science
- 3 years
- SQL
- Parental leave
11d
Associate Director, Contract Analytics
Sanofi —Morristown, NJ
- $148,500 - $214,500 a year
- Contract
- Hybrid work
- CPA
- Bachelor of Science
- 3 years
- Parental leave
Associate Director, Patient Experience, Respiratory
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- 5 years
- Bachelor of Science
- Bachelor's degree
- Paid holidays
- Health insurance
6d
Associate Director, Market Access Contracting
Sanofi —Morristown, NJ
- $148,500 - $214,500 a year
- Remote
- 5 years
- Bachelor's degree
- Continuous improvement
- Parental leave
Associate Director, Government Contracts
Eisai —Nutley, NJ
- $161,500 - $212,000 a year
- Full-time
- Hybrid work
- Office
- Master's degree
- 8 years
Associate Director, FP&A - Technical Operations
Insmed incorporated —New Jersey
- $155,000 - $201,500 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Oracle
- Microsoft Outlook
- Employee stock purchase plan
- Disability insurance
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
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Associate Director, Biostatistics (Late Stage)

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

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Job Details

$175,440 - $263,160 a year

Qualifications

Master's degree
Pharmaceutical company experience

Full Job Description

Job Title:
Associate Director, Biostatistics (Late Stage)

Job Requisition ID:
1282

Posting Start Date:
4/2/26

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

Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems.

Responsibilities

Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. Acts as main statistical contact for the assigned studies and projects. Provides guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data. Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile. CRO / Vendor Oversight: Review CRO/vendor proposal and budget. Establishes procedures through regular interaction, setting expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers on complex studies. Ensures deliverables are accurate and delivered according to the timelines. Global Health Authority Interaction / Negotiation: Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health Authorities Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.

Qualifications

Education Qualifications

Master's Degree in statistics or biostatistics required PhD in statistics or biostatistics preferred

Experience Qualifications

8+ Years of relevant experience in the pharmaceutical industry with a masters degree required

5+ Years of relevant experience in the pharmaceutical industry with a PhD preferred

Travel Requirements

Ability to travel up to 10% of the time.

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$175,440.00 - USD$263,160.00

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Professionals

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Refine Your Search

associate director pharmaceutical jobs in new jersey

Associate Director, Biostatistics (Late Stage)

Director, Clinical Operations - AAV

Associate Director Access & Reimbursement

Production Operator

Associate Director, Heplisav B

Associate Director, Statistical Programming

Associate Director, US Brand Marketing

Associate Director Biostatistics

Associate Director, P2P Marketing

Senior Scientist, Viral Vector Process Development - Downstream

Associate Director, Data Science - Market Access

Associate Director, Precision Medicine

Associate Director, Global Medical Cardiovascular, Mavacamten

Associate Director, Real World Evidence (RWE) Analytics

Associate Director, Contract Analytics

Associate Director, Patient Experience, Respiratory

Associate Director, Market Access Contracting

Associate Director, Government Contracts

Associate Director, FP&A - Technical Operations

Associate Director, Clinical Data Management

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