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Global Study Manager Jobs in Delaware (NOW HIRING)

Vialto Partners

Proposal Senior Manager

Dover, DE · On-site +1

As a team member at Vialto, you'll be part of a global network with real impact. We support 10,000 ... bios, and case studies, using content libraries and templated assets. Edit and proofread ...

Amgen

Imaging Specialist Manager

Wilmington, DE · On-site +1

Experience in operationalizing global clinical studies with imaging and vendor management * Good understanding of quality oversight and process improvement * Ability to network and establish ...

Straumann

Territory Manager - Delaware

Wilmington, DE · On-site

Why Straumann? • Global Market Leader: The Straumann Group has built a distinguished legacy as a ... Actively participate in Study Clubs, ensuring Straumann presentations are delivered and ...

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Global Study Manager information

See Delaware salary details

$23K

$61.4K

$102.6K

How much do global study manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for global study manager in Delaware is $61,404.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,100.00 per year, depending on experience, location, and employer.

How does a global study manager collaborate with cross-functional teams during a clinical trial?

A Global Study Manager plays a pivotal role in coordinating with cross-functional teams, such as clinical operations, data management, regulatory affairs, and safety teams, to ensure smooth execution of clinical trials. They facilitate regular meetings, provide clear communication on study timelines and deliverables, and address any issues that arise across different geographic regions. Effective collaboration is crucial for aligning global processes, maintaining data consistency, and meeting regulatory requirements, making strong interpersonal and project management skills essential for success in this role.

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

To excel as a Global Study Manager, you need expertise in clinical trial management, regulatory requirements, and project leadership, often backed by a life sciences degree and experience in global studies. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Excellent organizational skills, cross-cultural communication, and problem-solving abilities are vital soft skills for this role. These skills ensure effective coordination of international studies, compliance with regulations, and the successful delivery of complex clinical projects.

What does a global study manager do?

A global study manager oversees the planning, execution, and management of clinical research studies across multiple regions or countries. They coordinate with cross-functional teams, ensure compliance with regulatory requirements, and monitor study progress using project management tools to meet deadlines and quality standards.

What are popular job titles related to Global Study Manager jobs in Delaware?

For Global Study Manager jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Global Study Manager jobs in Delaware look for?

The top searched job categories for Global Study Manager jobs in Delaware are:

What cities in Delaware are hiring for Global Study Manager jobs?

Cities in Delaware with the most Global Study Manager job openings:

Global Study Manager jobs near you
Infographic showing various Global Study Manager job openings in Delaware as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $61,404 per year, or $29.5 per hour.

Specialist Study Management

US Tech Solutions

Wilmington, DE

$33.75 - $45.25/hr

Full-time

Re-posted 11 days ago

Key responsibilities

  • Set up, maintain, and close the local Trial Master File (eTMF) and Investigator Site File in compliance with ICH/GCP guidelines and local requirements.

  • Contribute to the production, maintenance, and import of study documents into the Global Electronic Library (GEL) according to the Global Document List (GDL).

  • Handle clinical-regulatory documents for electronic applications and submissions, ensuring compliance with technical standards and supporting publishing and delivery to regulatory authorities.

Job description

Company Description

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website www.ustechsolutions.com.

We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.

Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.

Job Description
  • Bachelor's degree is preferred
  • 3-5 years of experience in clinical trial DOCUMENT MANAGEMENT and regulatory documents is required
  • Operational responsibility to set-up the local Trial Master File (eTMF) and Investigator Site File including tracking of documents. Maintain and close the local TMF (in electronic or paper form depending on study) ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance and local requirements. Support the CRA in the maintenance and close out activities for the ISF.
  • Contribute to the production and maintenance of study documents, ensuring template and version compliance.
  • Create and/or import clinical-regulatory documents into the Global Electronic Library (GEL) according to the Global Document List (GDL) ensuring compliance with the Client Authoring Guide for Regulatory Documents to support publishing in GEL
  • Contribute to electronic applications/submissions by handling clinical-regulatory documents according to the requested technical standards i.e. Submission Ready Standards (SRS), supporting effective publishing and delivery to regulatory authorities
  • Set-up, populate and accurately maintain information in Client tracking and communication tools (e.g. IMPACT, SharePoint etc) and support others in the usage of these systems

Skills and Competencies

  • Experience with electronic trial master file system(s) including uploading, reviewing, QC, approval of study required documents.
  • Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines
  • Working knowledge of clinical study documents
  • Ability to develop advanced computer skills to increase efficiency in day-to-day tasks
  • Good verbal and written communication
  • Good interpersonal skills and ability to work in an international team environment
  • Willingness and ability to train others on study administration procedures
  • Display excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high volume environment with shifting priorities
  • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities
  • Integrity and high ethical standards
Qualifications
  • Experience with electronic trial master file system(s) including uploading, reviewing, QC, approval of study required documents.
Additional Information

Sneha Shrivastava

Sr Technical Recruiter

862 - 579 - 4236


US Tech Solutions logo

About US Tech Solutions

Sourced by ZipRecruiter

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.

Industry

It services

Company size

1,001 - 5,000 Employees

Headquarters location

Jersey City, NJ, US

Year founded

2000

Social media

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