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Clinical Study Manager Jobs in Edison, NJ (NOW HIRING)

IQVIA

Senior Global Clinical Study Manager

New York, NY · On-site

Required Experience * 2+ years of global study management experience * Experience across multiple countries/regions * Phase I-III clinical trials experience (Phase III required) * Oncology experience ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA ICON is a global ... Manages and maintains team SharePoint and/or shared drive sites, as needed * Communication with ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Manages and maintains team SharePoint and/or shared drive sites, as needed * Communication with ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Manages and maintains team SharePoint and/or shared drive sites, as needed * Communication with ...

Icon plc

Clinical Study Specialist

New York, NY · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Manages and maintains team SharePoint and/or shared drive sites, as needed * Communication with ...

ICON

Clinical Study Specialist

Warren, NJ · On-site

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Manages and maintains team SharePoint and/or shared drive sites, as needed * Communication with ...

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Clinical Study Lead

Warren, NJ · Hybrid

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Coordinates & manages various tasks in collaboration with other sponsor roles to achieve site ...

ICON

Clinical Study Lead

Warren, NJ · On-site +1

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Coordinates & manages various tasks in collaboration with other sponsor roles to achieve site ...

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Clinical Study Manager information

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$64

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How much do clinical study manager jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for clinical study manager in Edison, NJ is $64.72, according to ZipRecruiter salary data. Most workers in this role earn between $52.50 and $72.93 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

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

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Edison, NJ?

The most popular types of Clinical Study jobs in Edison, NJ are:

What are popular job titles related to Clinical Study Manager jobs in Edison, NJ?

For Clinical Study Manager jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Edison, NJ look for?

The top searched job categories for Clinical Study Manager jobs in Edison, NJ are:

What cities near Edison, NJ are hiring for Clinical Study Manager jobs?

Cities near Edison, NJ with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Edison, NJ as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $134,618 per year, or $64.7 per hour.

Clinical Study Manager

New York, NY • On-site

Global Channel Management, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Global Channel Management, Inc.external

$70/hr

Contractor

Re-posted 16 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

3-5 years
Strong Project Management
Regulatory submission experience
Oncology experience
Participate on a cross functional team focused on US regulatory submissions (FDA).
* Previous Pfizer experience is preferred; Pharmaceutical/biotech experience mandatory.
Familiarity with U.S. NDA processes required
Provides Financial Oversight
Forecasts and manages high level clinical trial budget. Oversees the study risk planning process (e.g. IQMP)
Works proactively with AP/CRO
Supports Practical Clinical Trial Design
o Partners with Clinician and other team members and supporting functional lines to provide operational expertise and insight to inform protocol design.
o Initiates and ensures a Protocol Operational Feasibility and Budget assessment is performed by seeking input from other lines within Development Operations and at the Alliance Partner/Vendor as needed.
o Facilitates early engagement of Alliance Partners/Vendors when needed.

Additional Information

$70/hr

6  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

Year founded

2009

Social media

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