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

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 ...

These studies are conducted within the standards set by Bayer and according to Good Clinical Practices (GCP) and applicable regulatory and legal requirements. The Sr. Study Manager manages all study ...

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Clinical Study Manager information

See Summit, NJ salary details

$30

$66

$102

How much do clinical study manager jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical study manager in Summit, NJ is $66.43, according to ZipRecruiter salary data. Most workers in this role earn between $53.89 and $74.86 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.
What job categories do people searching Clinical Study Manager jobs in Summit, NJ look for? The top searched job categories for Clinical Study Manager jobs in Summit, NJ are:
What cities near Summit, NJ are hiring for Clinical Study Manager jobs? Cities near Summit, NJ with the most Clinical Study Manager job openings:
Infographic showing various Clinical Study Manager job openings in Summit, NJ as of August 2026, with employment types broken down into 79% Full Time, 16% Part Time, 3% Temporary, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $138,174 per year, or $66.4 per hour.

Full-time

Re-posted 12 days ago


Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Medical Affairs - Global Oncology 

Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments. 

Assist in the management of the Trial Master File (submit documents, reconciliation, QC, etc.).

Participate in development of protocol, case report form, CRF guidelines and other study documents. 

Prepare and/or review regulatory documents (e.g. ICF), contracts, requests for proposal. 

Ensure the training of CROs/investigators on protocol, regulatory, Eisai SOPs and data issues. Reviews and approves monitoring reports and ensures tracking of ongoing site issues. On-site Monitoring 

Minimum of college degree in a relevant discipline. 

Bachelor's degree in relevant scientific discipline preferred. 

CANDIDATES MUST HAVE MIN 3-5 years in-house in pharma company. Not just 3-5 years in CRO or onsite monitoring. We want to see associate in-house large pharma.

Want to see experience in phase 1-3 global study trials in multifunctional areas. 

MUST HAVE experience in reviewing patient data and patient profiles



Qualifications

**Oncology Experience Highly Preferred.**

Additional Information

Best Regards,

Sneha Shrivastava

973-967-3348

 



Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992