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Clinical Trials Manager Jobs in Raritan, NJ (NOW HIRING)

Vitalief

Clinical Research Coordinator

New Brunswick, NJ · On-site

$60 - $70/hr

Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus. PHYSICAL DEMANDS Standing, sitting, walking, talking, hearing, and visual ...

Vitalief

Clinical Research Coordinator

New Brunswick, NJ · On-site

$60K - $70K/yr

Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus. PHYSICAL DEMANDS: Standing, sitting, walking, talking, hearing, and visual ...

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All JobsClinical Trials JobsClinical Trials Manager JobsClinical Trials Manager Jobs in Raritan, NJ

Clinical Trials Manager information

See Raritan, NJ salary details

$29

$64

$98

How much do clinical trials manager jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical trials manager in Raritan, NJ is $64.02, according to ZipRecruiter salary data. Most workers in this role earn between $51.92 and $72.12 per hour, depending on experience, location, and employer.

What does a clinical trials manager do?

A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.

What are some common challenges faced by clinical trials managers and how can they be addressed?

Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.

What are the key skills and qualifications needed to thrive as a clinical trials manager, and why are they important?

To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.

What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?

AspectClinical Trials ManagerClinical Research Coordinator
ResponsibilitiesOversees entire clinical trial process, manages teams, ensures compliance, and handles budgets.Assists with patient recruitment, data collection, and site coordination under supervision.
Required CredentialsBachelor’s or higher in life sciences, often with project management experience.Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred.
Work EnvironmentWorks in clinical trial sites, research organizations, or pharmaceutical companies.Primarily works at clinical sites, hospitals, or research facilities.

In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Trials jobs in Raritan, NJ?

The most popular types of Clinical Trials jobs in Raritan, NJ are:

What job categories do people searching Clinical Trials Manager jobs in Raritan, NJ look for?

The top searched job categories for Clinical Trials Manager jobs in Raritan, NJ are:

What cities near Raritan, NJ are hiring for Clinical Trials Manager jobs?

Cities near Raritan, NJ with the most Clinical Trials Manager job openings:

Clinical Trials Manager jobs near you
Infographic showing various Clinical Trials Manager job openings in Raritan, NJ as of August 2026, with employment types broken down into 78% Full Time, 17% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $133,160 per year, or $64 per hour.

CLINICAL TRIALS MANAGER

Global Channel Management, Inc.

Raritan, NJ • On-site

$44/hr

Contractor

Re-posted 7 days ago

Job description

Company Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. 


Qualifications

Qualifications

  • Bachelor Degree required, preferably in biological or medical sciences.  Master's Degree or higher is desirable.  
  • Minimum
    of 8 years direct clinical research experience, of which a minimum of 4
    years clinical research supervisory or management capacity with
    budgetary responsibility.
  • Knowledge of applicable standards and regulations for clinical trial and laboratory conduct
  • Proven oral and written communication skills
  • Proven planning skills; ability to create and track detailed project plans
  • Proven interpersonal, leadership and organizational skills & Effective time management
  • Ability
    to work independently and within a cross-functional team environment to
    analyze and solve problems, and to make sound decisions
  • Basic biostatistical knowledge
  • Must
    be willing to periodically work with potentially biohazardous materials
    in an approved safe manner and to work in biohazardous environments
  • Demonstrated experience in computer skills to include Microsoft Word, Excel and basic templates

Preferred:

  • 2 years IVD Monitoring experience
  • Experience in Cardiac clinical studies
  • Strong technical lab expertise with demonstrated ability in assay analysis and data interpretation
Additional Information

$44/hr

12 months

Global Channel Management logo

About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

Social media

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