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Study Com information

See Summit, NJ salary details

$23.4K

$133.1K

$218.9K

How much do study com jobs pay per year?

As of Jun 23, 2026, the average yearly pay for study com in Summit, NJ is $133,133.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,300.00 and $166,800.00 per year, depending on experience, location, and employer.

How much does Study.com pay?

Study.com offers various roles such as content creators and educators, with pay rates typically ranging from $15 to $30 per hour depending on the position and experience. Compensation may also include bonuses or incentives based on performance and project requirements.

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 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.

How to make $10,000 a month with no degree?

Study Com roles such as online tutoring, freelance writing, or digital marketing can generate high income without a degree by leveraging skills, building a strong portfolio, and using platforms like Upwork or Fiverr. Success depends on experience, reputation, and consistent effort to scale income over time.

Is study.com legit to work for?

Study.com offers various remote teaching and content creation positions, and many employees report it as a legitimate employer. However, as with any job opportunity, it is advisable to research current reviews and verify the specific role's requirements before applying.

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.

How can I make 2000 a week working from home?

Study Com and similar remote roles often pay based on the number of completed tasks or hours worked, with earnings varying by workload and efficiency. To make $2000 a week, you typically need to work full-time hours consistently, develop strong study or communication skills, and possibly hold relevant certifications or experience to increase earning potential.
What job categories do people searching Study Com jobs in Summit, NJ look for? The top searched job categories for Study Com jobs in Summit, NJ are:
What cities near Summit, NJ are hiring for Study Com jobs? Cities near Summit, NJ with the most Study Com job openings:
Study Com jobs near you
Infographic showing various Study Com job openings in Summit, NJ as of June 2026, with employment types broken down into 2% As Needed, 81% Full Time, 13% Part Time, 2% Temporary, 1% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $133,133 per year, or $64 per hour.
Senior Study Manager

Senior Study Manager

US Tech Solutions

Jersey City, NJ • On-site

Contractor

Posted 10 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

Job Description:

The Senior Study Manager manages and is responsible for all aspects of assigned Phase I and extended Phase I/II a complex clinical trials, within the approved Clinical Sciences Development Plan (CSDP). 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 related activities from approved study concept to the final clinical research report (CSR) and ensures that study execution is on track. As a member of the Operational Sub-team of the ECT/CST he/she provides input to this team to ensure there is accurate tracking. Within the framework given by the ECL/CPL and the OPL, the Sr. Study Manager develops controls and is accountable for the overall study budget and informs the team on budget issues and/or concerns. The Sr. Study Manager implements, manages and leads a
cross functional study team for the entire duration of the study. The overall objective for the Sr. Study Manager is to manage the planning, implementation, analysis and reporting of assigned clinical pharmacology studies within the established timelines and budget, ensuring high quality of study conduct and data obtained as well as all requirements necessary for global regulatory approvals. The Sr. Study Manager is expected to proactively provide and implement ideas and suggestions for global process improvement efforts.

Sr. Study Manager Job description

The incumbent will:

Manages and is responsible for all activities related to clinical pharmacology, complex phase I, extended phase I/II a oncology clinical trials from the approved study concept to the clinical study report.

Manages all Study Team activities as defined per SOPs/OIs and ensures the organization of

regular Study Team meetings

Manages the selection and oversight of External Suppliers (e.g. site management and monitoring CROs, Central Labs, central ECG reading center, etc.)

Develops and manages budget, timelines and quality of the study and its deliverables.

Responsible for forecasting and tracking of study costs. Ensuring all relevant IT-systems are updated with current and accurate information (e.g. IMPACT)

Responsible for all start up activities e.g. CRO selection, CRF development, drug forecasting, study manuals, monitoring plan, data management plan, definition of end points, selection of

safety and efficacy assessments, recruitment planning and oversight.

Writes protocols and amendments in collaboration with study team members

Responsible for study specific feasibility and site selection to meet study enrollment and

timelines.

Together with OPL and ECL/CPL responsible for developing the total external study budget and accountable for providing monthly and yearly estimates, tracking study budget, initiating

payments, providing monthly information to controlling, OPL, ECL/CPL, identifying budget/estimate issues and proactively developing a plan for resolving study finance issues.

Tracks and compiles patient enrollment, data quality and cleaning progress and overall study progress and ensures study timelines are met

Responsible for training and oversight of CROs to ensure compliance with timelines and budget.

Develops appropriate study related training for monitors and site personnel according to GCP

and company standards

The incumbent is responsible for the direct management of Phase I & IIa complex oncology global clinical trials. This requires an in-depth knowledge of study management/project management. In addition Good Clinical Practices (GCP), federal regulations and international regulations (International Harmonization Committee-ICH regulations).

The position also requires strong awareness and understanding of cultural differences as well as regional operational differences.

Demonstrated leadership in project management and vendor management.

The incumbent requires comprehensive knowledge of the drug development process including, monitoring, regulatory requirements, drug safety requirements, data management processes and budget parameters.

Effective written and verbal communication, thorough knowledge of oral and written English, strong oral presentation, and excellent interpersonal, decision-making and issue resolution skills are required. In addition, the incumbent requires effective planning and organization skills, attention to detail and excellent follow through.

Qualifications

Qualifications

Bachelor's degree or equivalent education with 8+ years of relevant healthcare experience of which 5 years working in early clinical operations pharmaceutical (preferably oncology) including direct monitoring and clinical trial/study management experience.

Ideal candidate will have solid clinical operations experience working as a study manager including 2 years of monitoring experience and a minimum of 3 years of study management (early oncology) experience is preferred

Additional Information

Richha Saini

Senior Clinical/Pharmaceutical Recruiter

Tel: (201) 524 9600 Ext 7179

Direct: 781-262-3067

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

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