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Study Com Jobs in Delaware (NOW HIRING)

US Tech Solutions

Specialist Study Management

Wilmington, DE · On-site

$33.75 - $45.25/hr

To know more about US Tech Solutions, please visit our website www.ustechsolutions.com. We are ... Maintain and close the local TMF (in electronic or paper form depending on study) ensuring ...

TechTrueUp

Clinical Scientist

Newark, DE · On-site +1

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE ... Prepare clinical documentation such as Investigator Brochures, Clinical Study Protocols, and ...

SA Technologies Inc.

Accountant

Newark, DE · On-site

Company Description SA Technologies Inc. (www.satincorp.com) is a market leader and one of the ... studies. Respond to data requests from Regulatory Commissions, the Internal Revenue Service and/or ...

Techtrueup

Clinical Scientist

Newark, DE · Remote

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE ... Prepare clinical documentation such as Investigator Brochures, Clinical Study Protocols, and ...

Techtrueup

Clinical Scientist

Newark, DE · On-site

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE ... Prepare clinical documentation such as Investigator Brochures, Clinical Study Protocols, and ...

Techtrueup

Clinical Scientist

Newark, DE · Remote

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE ... Prepare clinical documentation such as Investigator Brochures, Clinical Study Protocols, and ...

MMS

Principal Biostatistician - Remote

Wilmington, DE · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. Roles and Responsibilities * Lead complex ... Provide valuable feedback to the Sponsor on the statistical aspects of the study. * Prepare and ...

State of Delaware

Internship Opportunity

Dover, DE · On-site

For your convenience, you will be able to select your preferred location and field of study when ... com. You may also call (302) 739-5458 or email DHR_ADAConcerns@delaware.gov for additional ...

Mesa Associates Inc.

Substation Design Engineer

Newark, DE · On-site

$97.10K - $123.70K/yr

Be cautious and only respond to emails from our "mesainc.com" domain. We will never ask for ... May also complete Lightning Studies, Illumination Studies, Rigid Bus Evaluations, and Conduit Fill ...

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Study Com information

See Delaware salary details

$22K

$125.4K

$206.2K

How much do study com jobs pay per year?

As of May 31, 2026, the average yearly pay for study com in Delaware is $125,398.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,100.00 and $157,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What are the typical responsibilities of a Study Coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What are Study Com jobs?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

What job categories do people searching Study Com jobs in Delaware look for? The top searched job categories for Study Com jobs in Delaware are:
What cities in Delaware are hiring for Study Com jobs? Cities in Delaware with the most Study Com job openings:
Study Com jobs near you
Specialist Study Management

Specialist Study Management

US Tech Solutions

Wilmington, DE • On-site

$33.75 - $45.25/hr

Other

Posted 4 days ago

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


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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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