Top 628 Pharmaceutical clinical Jobs in Princeton, Nj

Senior Clinical Trial Manager
Genmab —Princeton, NJ
- $130,720 - $196,080 a year
- Online Application
- Master's degree
- 8 years
- Bachelor's degree
- Commuter assistance
- Paid parental leave
12d
Biologics Pharma Sales Rep
Prism Biotech —Princeton, NJ
- $85,409 - $116,661 a year
- Full-time
- Organizational skills
- Leadership
- Communication skills
Quick Apply
Pharma Sales Account Rep
Prism Biotech —Plainfield, NJ
- $86,030 - $117,282 a year
- Full-time
- Mid-level
- Continuous improvement
- Commercial
Quick Apply
Clinical Trial Manager
Genmab —Princeton, NJ
- $119,120 - $178,680 a year
- Online Application
- 5 years
- Master's degree
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Programming Manager, Clinical Programming
Genmab —Princeton, NJ
- $117,840 - $176,760 a year
- Online Application
- Computer science
- Computer Science
- Writing skills
- Commuter assistance
- Paid parental leave
CLINICAL TRIAL ASSOCIATE (multiple openings)
Zenith LifeScience —South Plainfield, NJ
- $111,925 a year
- Full-time
- Mid-level
- Travel
- Experience equivalent to degree accepted
DRUG SAFETY ASSOCIATE (multiple openings)
Zenith LifeScience —South Plainfield, NJ
- $111,925 a year
- Full-time
- Mid-level
- Travel
- Scripting
Quality Assurance / Document Control
Sciecure Pharma Inc. —Monmouth Junction, NJ
- Full-time
- 3 years
- Bachelor's degree
- Organizational skills
Clinical Scientist
SystImmune —Princeton, NJ
- $80,000 - $130,000 a year
- Full-time
- Mid-level
- Leadership
- Communication skills
- Paid holidays
- Disability insurance
Clinical Research Associate- West Coast
Zydus Therapeutics Inc. —Pennington, NJ
- $100,000 - $110,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
MEDICAL REVIEWER
Zenith LifeScience —South Plainfield, NJ
- $100,000 - $120,000 a year
- Full-time
- Medicine
- Microsoft Excel
- English
CLINICAL DATA MANAGER
Zenith LifeScience —South Plainfield, NJ
- $100,000 - $120,000 a year
- Full-time
- Bachelor of Science
- Math
- Bachelor's degree
Clinical Research Coordinator
Saint Peter's University Healthcare System —New Brunswick, NJ
- $54,018 - $86,445 a year
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
- Free parking
- Health insurance
Quick Apply
Project Coordinator / Assistant
Insmed Incorporated —Bridgewater, NJ
- $54 - $69 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Employee stock purchase plan
- Disability insurance
BioPharma Account Rep
Prism Biotech —Edison, NJ
- $85,136 - $116,388 a year
- Full-time
- Mid-level
- Continuous improvement
- Commercial
Quick Apply
Medical Writer
SystImmune —Princeton, NJ
- $80,000 - $130,000 a year
- Full-time
- Mid-level
- Office
- Master's degree
- Paid holidays
- Disability insurance
Scientist I, Process Development
Legend Biotech US —Somerset, NJ
- $96,267 - $126,351 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Regulatory Affairs Specialist
Amneal Pharmaceuticals —Piscataway, NJ
- $117,000 - $120,000 a year
- Full-time
- 5 years
- Mid-level
- Office
Translational Scientist
ADLAI NORTYE USA INC —North Brunswick, NJ
- Full-time
- Analysis skills
- Doctor of Philosophy
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Computer System Validation Engineer
Katalyst Healthcares & Life Sciences —Princeton, NJ
- Contract
- Hybrid work
- Computer Science
- Mid-level
- Bachelor's degree
Quick Apply

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pharmaceutical clinical jobs near princeton, nj

Senior Clinical Trial Manager

Genmab -
Princeton, NJ

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Job Details

Full-time
$130,720 - $196,080 a year
12 days ago

Benefits

Commuter assistance
Paid parental leave
Health savings account
Paid holidays
Health insurance
Dental insurance
Tuition reimbursement
Parental leave
Vision insurance
401(k) matching

Qualifications

Bachelor's degree

Full Job Description

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

About the Role

At Genmab, we’re dedicated to developing and delivering innovative antibody-based therapeutics to improve the lives of patients. As a Senior Clinical Trial Manager (CTM), you will play a pivotal role in driving the success of our clinical trials through strategic oversight, operational excellence, and cross-functional collaboration.

The Senior CTM partners closely with Clinical Trial Teams (CTTs), service providers, and investigators to ensure that our clinical studies are executed on time, within budget, and in full compliance with regulatory standards and Genmab’s high-quality expectations. This role offers the opportunity to work in a dynamic, global, and matrixed environment where you will be empowered to take ownership and lead with autonomy.

Key Responsibilities

Lead the operational planning, setup, and execution of global clinical trials, ensuring delivery on time, and in compliance with regulatory and quality standards.
Oversee trial documentation and systems, ensuring accuracy, completeness, and continuous inspection readiness.
Drive site feasibility, selection, and activation strategies in collaboration with CROs and internal stakeholders.
Manage and oversee CROs and other service providers, ensuring high-quality deliverables, adherence to timelines, and effective collaboration.
Proactively identify, assess, and mitigate operational risks using risk-based quality management approaches.
Oversee protocol deviations, issue management, and ensure appropriate escalation and resolution of trial-level challenges.
Monitor trial performance and data quality, leveraging key metrics to drive decision-making and continuous improvement.
Act as a key cross-functional leader, fostering strong collaboration across internal teams, vendors, and investigators.

Qualifications

Bachelor’s degree in life sciences or related field (Master’s degree preferred).
8+ years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
Solid understanding of ICH/GCP regulations and the clinical drug development lifecycle.
Proven experience managing global, multi-center trials and working in a complex, matrixed organization.
Strong project management and service provider oversight skills.
Excellent communication, collaboration, and interpersonal skills.
Oncology and/or therapeutic area–specific experience is highly desirable.
Ability to lead without authority and mentor others in a cross-functional environment.

For US based candidates, the proposed salary band for this position is as follows:

$130,720.00-$196,080.00

The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you’re joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:

401(k) Plan: 100% match on the first 6% of contributions
Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

Further details on eligibility for compensation and benefits based on role will be provided during the recruitment process

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).

Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

Apply Now

Refine Your Search

pharmaceutical clinical jobs in princeton, nj

Senior Clinical Trial Manager

Biologics Pharma Sales Rep

Pharma Sales Account Rep

Clinical Trial Manager

Programming Manager, Clinical Programming

CLINICAL TRIAL ASSOCIATE (multiple openings)

DRUG SAFETY ASSOCIATE (multiple openings)

Quality Assurance / Document Control

Clinical Scientist

Clinical Research Associate- West Coast

MEDICAL REVIEWER

CLINICAL DATA MANAGER

Clinical Research Coordinator

Project Coordinator / Assistant

BioPharma Account Rep

Medical Writer

Scientist I, Process Development

Regulatory Affairs Specialist

Translational Scientist

Computer System Validation Engineer

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