Top 69 Clinical trial manager Jobs in Somerville, Nj

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
Manager, Clinical Pharmacology
EPM Scientific —Princeton, NJ
- $130,000 - $150,000 a year
- Medicine
- 5 years
- Doctor of Philosophy
Quick Apply
5d
Associate Director - External Data Acquisition Lead (EDAL)
Genmab —Plainsboro, NJ
- $157,360 - $236,040 a year
- Online Application
- Master's degree
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave
Clinical Program Manager
IQVIA —Parsippany-Troy Hills, NJ
- $93,100 - $285,500 a year
- Full-time
- Remote
- Bachelor's degree
- Conflict management
- Senior level
- Work from home
Clinical Program Manager
Kite Pharma —Parsippany-Troy Hills, NJ
- $165,495 - $235,620 a year
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Dental insurance
Junior / Lower Mid-Level - Clinical Trial Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Microsoft Outlook
- English
- Mid-level
Quick Apply
5d
Clinical Study Associate Manager
Regeneron —Warren, NJ
- $109,900 - $179,300 a year
- Bachelor's degree
- Team management
- Travel
- Health insurance
- Dental insurance
Clinical Research Manager, Immunology, Remote
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- Remote
- 5 years
- English
- Bachelor's degree
- Paid holidays
- Health insurance
2h
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
Clinical Trial Liaison Manager
Recordati —Bridgewater, NJ
- $109,800 - $164,700 a year
- Weekends as needed
- Hybrid work
- 5 years
- English
- Mid-level
- AD&D insurance
- Paid holidays
Clinical Trial Manager/Senior Clinical Trial Manager
Precision for Medicine —Gladstone, NJ
- $110,700 - $200,900 a year
- Online Application
- Remote
- 7 years
- Microsoft Excel
- Microsoft Outlook
Quick Apply
11d
CLINICAL DATA MANAGER
Zenith LifeScience —South Plainfield, NJ
- $100,000 - $120,000 a year
- Full-time
- Bachelor of Science
- Math
- Bachelor's degree
Manager, Clinical Study Lead
Regeneron —Warren, NJ
- $128,600 - $210,000 a year
- Microsoft Word
- Microsoft Excel
- 6 years
- Health insurance
- Dental insurance
Sr. Clinical Trial Manager, Therapeutics and Oncology
Moderna, Inc. —Princeton, NJ
- $130,800 - $209,400 a year
- Full-time
- 5 years
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
Contracts Manager, Clinical Supply Services
Catalent —Bridgewater, NJ
- $122,000 - $160,000 a year
- Email
- Writing skills
- Mid-level
- Office
- Paid holidays
- Health insurance
7d
Senior Project Manager Clinical Research
Abbott Laboratories —Princeton, NJ
- $86,700 - $173,300 a year
- Full-time
- Office
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Tuition reimbursement
Title Clinical Trial Liaison Manager
Recordati —Bridgewater, NJ
- $109,800 - $164,700 a year
- Weekends as needed
- Hybrid work
- 5 years
- English
- Mid-level
- AD&D insurance
- Paid holidays
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
Senior Manager, Clinical Data Systems
AbbVie —Florham Park, NJ
- $124,500 - $236,500 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- SQL
- Paid holidays
- Health insurance

I want to receive the latest job alert for clinical trial manager in somerville, nj

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical trial manager jobs near somerville, nj

Contract Manager jobs in Bridgewater, NJ

Clinical Trial Manager jobs in Princeton, NJ

Clinic Manager jobs in Princeton, NJ

Clinical Program Manager jobs in Parsippany-Troy Hills, NJ

Senior Project Manager jobs in Princeton, NJ

Contract Manager jobs in Marietta, GA

Contract Manager jobs in Oklahoma City, OK

Case Manager jobs in Denton, TX

Contract Administrator jobs in Los Angeles, CA

Construction Project Manager jobs in Portland, OR

Contract Jobs jobs in Boston, MA

Contract Manager jobs in Rockville, MD

Contract Manager jobs in State College, PA

Non Clinical Social Work jobs in Tampa, FL

Clinical Trial Manager jobs in Dallas, TX

Clinical Trial Manager jobs in Houston, TX

Clinical Trial Manager jobs in Michigan

Practice Manager jobs in Charlotte, NC

Clinical Trial Manager jobs in Tucson, AZ

Clinical Trial Manager jobs in San Diego, CA

Programming Manager, Clinical Programming

Genmab -
Princeton, NJ

Apply Now

Job Details

Full-time
$117,840 - $176,760 a year

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

SAS
Employee relationship building
English
SAS language
Bachelor's degree
Pharmaceutical company experience
International corporation experience
Data analysis software

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!

The Role

Work arrangement: This role offers flexibility to work away from the office for 20%–40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager.

Responsibilities/tasks – including but not limited to:

Implements and assists on developing company Study Data Tabulation Model (SDTM) standards that support the scientific need of a study/program while ensuring quality, consistency and compliance to CDISC standards and other industry standards that supports the exchange of data, reporting, and analysis
Ensures alignment of SDTM standards with data collection standards and relevant company tools/system requirements by reviewing study eCRFs, supporting creation of external data collection standards, and providing SDTM mapping guidance
Ensures study or portfolio-level SDTM datasets are in compliance with CDISC and regulatory submission requirements, reviews study submission data packages to ensure quality and integrity
Creates quality control processes, metrics and other measures to ensure compliance with standards
Ensures work carried out in accordance with applicable SOP’s and working practices, as well as global agency regulations/guidance’s
Supports developing and reviewing standard processes and templates.
Working with Digital Solutions and IT, support the implementation of future strategies and technology-enabled processes and tools for clinical trials standards, change control management and the exchange of standards information to internal downstream consumers and externally consumers
Supports development of GenSense Dashboards by providing guidance on data structure, organization and contents of the Genmab SDTM-databases to the Dashboard developers and programmers
Produce other in-house checks of data consistencies
Contributes to knowledge sharing, skill building and good collaboration with stakeholders and colleagues
Contributes to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge

Maintains up-to-date knowledge on relevant regulatory guidelines/requirements
Maintains a good working relationship with stakeholders and colleagues
Participates and represent clinical programming in teams and meetings

Requirements:

Bachelor’s degree in Statistics, Computer Science, Life Sciences. Master’s degree in Statistics, Computer Science, Life Sciences preferred
Has experience working in a global context
Proficient in both written and spoken English
At least 3-5 years of experience within the pharmaceutical industry
Has experience with the SAS software package

As Programming Manager, Clinical Programming, it is expected that the employee:

Acts as a role model
Leads programming study team in an effective and professional manner
Proactively engages in department activities
Arranges lessons learned to share learnings
Leads various initiatives within the department
Proactively contributes to support a global organization
Acts as mentor for new employees or consultants

Competences and skills:

SAS programming
Analytical and problem-solving skills
Expert knowledge of the CDISC SDTM data model: the corresponding structures and organizations of the data.
Contextual understanding of the data
Writes efficient, easily maintained and well documented computer programs
Is systematic and organized in writing and archiving computer programs
Proactive and Accountable and Goal oriented
Innovative
Good team player
Good at sharing knowledge
Works independently, take responsibility and show initiative
Good communication skills
Good planning and coordinating skills
Ability to flexibly work on multiple tasks without compromise of the quality of the work

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

$117,840.00-$176,760.00

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

clinical trial manager jobs in somerville, nj

Programming Manager, Clinical Programming

Manager, Clinical Pharmacology

Associate Director - External Data Acquisition Lead (EDAL)

Clinical Program Manager

Clinical Program Manager

Junior / Lower Mid-Level - Clinical Trial Manager

Clinical Study Associate Manager

Clinical Research Manager, Immunology, Remote

Clinical Trial Manager

Clinical Trial Liaison Manager

Clinical Trial Manager/Senior Clinical Trial Manager

CLINICAL DATA MANAGER

Manager, Clinical Study Lead

Sr. Clinical Trial Manager, Therapeutics and Oncology

Senior Clinical Trial Manager

Contracts Manager, Clinical Supply Services

Senior Project Manager Clinical Research

Title Clinical Trial Liaison Manager

Senior Clinical Trial Manager

Senior Manager, Clinical Data Systems

I want to receive the latest job alert for clinical trial manager in somerville, nj

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected