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

Gilead

Director, Clinical Operations

Parsippany, NJ · On-site

$210K - $272K/yr

... direct impact. We believe every employee deserves a great leader. People Leaders are the ... Prior experience leading and overseeing oncology clinical trials with a minimum of 5 years ...

Gilead

Director, Clinical Operations

Parsippany, NJ · On-site

$210K - $272K/yr

... direct impact. We believe every employee deserves a great leader. People Leaders are the ... Prior experience leading and overseeing oncology clinical trials with a minimum of 5 years ...

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

Clinical Trials Director information

See Raritan, NJ salary details

$10

$55

$119

How much do clinical trials director jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trials director in Raritan, NJ is $55.64, according to ZipRecruiter salary data. Most workers in this role earn between $33.22 and $73.37 per hour, depending on experience, location, and employer.

What does a clinical trials director do?

A Clinical Trials Director oversees the planning, execution, and management of clinical research trials to ensure they are conducted ethically, safely, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and ensure that trials meet scientific and operational objectives. Their responsibilities also include liaising with regulatory agencies, monitoring trial progress, and addressing any issues that arise during the study.

What are the key skills and qualifications needed to thrive as a clinical trials director?

To thrive as a Clinical Trials Director, you need a strong background in clinical research, regulatory compliance, and project management, typically supported by an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are commonly required. Exceptional leadership, strategic thinking, and communication skills are crucial for managing cross-functional teams and stakeholder relationships. These competencies ensure successful trial execution, regulatory adherence, and the delivery of safe and effective clinical outcomes.

What are some common challenges faced by a clinical trials director and how can they be managed?

Clinical Trials Directors often encounter challenges such as coordinating large, cross-functional teams, ensuring strict regulatory compliance, and managing tight timelines for multiple studies. Effective communication, strong leadership, and proactive risk management are essential to address these issues. Staying updated on regulatory changes and fostering collaboration between departments can also help streamline processes and ensure trials run efficiently.

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

AspectClinical Trials DirectorClinical Research Manager
ResponsibilitiesOversees entire clinical trial programs, manages teams, and ensures regulatory complianceManages daily operations of clinical research projects, coordinates activities, and supports trial execution
Required CredentialsTypically requires a clinical research or life sciences degree, with extensive experienceRequires similar degrees and experience, often with less strategic oversight
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple projectsOperational roles within research sites or CROs, focusing on project execution

The Clinical Trials Director focuses on strategic oversight and leadership of clinical trial programs, while the Clinical Research Manager handles day-to-day project management. Both roles require relevant credentials and industry experience, but differ in scope and level of responsibility.

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 Director jobs in Raritan, NJ look for?

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

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

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

Clinical Trials Director jobs near you
Infographic showing various Clinical Trials Director job openings in Raritan, NJ as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $115,726 per year, or $55.6 per hour.

CLINICAL TRIALS MANAGER

Global Channel Management, Inc.

Raritan, NJ • On-site

$44/hr

Contractor

Re-posted 8 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

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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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