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Study Com Jobs in Connecticut (NOW HIRING)

US Tech Solutions

Scientist IV

Ridgefield, CT · On-site

To know more about US Tech Solutions, please visit our website www.ustechsolutions.com. We are ... Provide dose formulation stability testing for GLP studies. Develop and validated analytical ...

VillageMD

Per Diem Xray Technologist

New Britain, CT · On-site

... summithealth.com, @citymd.net, @villagemd.com, @villagemedical.com, @westmedgroup.com ... Verify proper patient identification on the study and route it PACS. Send required information to ...

VillageMD

Per Diem CT Technologist

New Britain, CT · On-site

... summithealth.com, @citymd.net, @villagemd.com, @villagemedical.com, @westmedgroup.com ... Process studies onto CD for patient study requests while maintaining proper HIPPA compliance.

VillageMD

Float X-Ray Technologist

Greenwich, CT · On-site

... summithealth.com, @citymd.net, @villagemd.com, @villagemedical.com, @westmedgroup.com ... Verify proper patient identification on the study and route it PACS. Send required information to ...

VillageMD

Per Diem CT Technologist

New Britain, CT · On-site

... summithealth.com, @citymd.net, @villagemd.com, @villagemedical.com, @westmedgroup.com ... Process studies onto CD for patient study requests while maintaining proper HIPPA compliance.

VillageMD

Float X-Ray Technologist

Greenwich, CT

... summithealth.com, @citymd.net, @villagemd.com, @villagemedical.com, @westmedgroup.com ... Verify proper patient identification on the study and route it PACS. Send required information to ...

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All JobsStudy Com JobsStudy Com Jobs in Connecticut

Study Com information

See Connecticut salary details

$20.9K

$119.2K

$196K

How much do study com jobs pay per year?

As of Aug 3, 2026, the average yearly pay for study com in Connecticut is $119,187.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,900.00 and $149,400.00 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 jobs pay 4000 a week without a degree?

Study Com is a company that offers online tutoring and educational services, but generally, jobs that pay $4,000 a week without a degree include high-paying sales roles, real estate agents, commercial pilots, or skilled trades like electricians and plumbers with experience. These positions often require specialized skills, certifications, or licenses and may involve variable schedules or commission-based pay structures.

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.

Is study.com legit to work for?

Study.com offers various remote teaching and content creation positions, and many employees report legitimate employment opportunities. However, as with any online job platform, it is advisable to research specific roles, review current employee feedback, and ensure the job posting is official 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 sessions, with earnings varying by workload and efficiency. To reach $2000 weekly, you may need to work full-time hours, develop specialized skills, and maintain consistent productivity. Building a strong reputation and gaining certifications can also help increase earning potential in such roles.
What are popular job titles related to Study Com jobs in Connecticut? For Study Com jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Study Com jobs in Connecticut look for? The top searched job categories for Study Com jobs in Connecticut are:
What cities in Connecticut are hiring for Study Com jobs? Cities in Connecticut with the most Study Com job openings:
Study Com jobs near you
Infographic showing various Study Com job openings in Connecticut as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $119,187 per year, or $57.3 per hour.

Principal Statistical Programmer - Global Studies- REMOTE

Penfield Search Partners

Fairfield, CT • Remote

Other

Re-posted 21 days ago

Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates We are seeking a highly experienced Statistical Programmer to lead programming activities across global clinical studies. This role operates beyond executional programming, with responsibility for oversight of CRO deliverables, validation of outputs, and end-to-end accountability for statistical programming packages. Key Responsibilities Lead statistical programming activities across global studies Serve as primary programming lead in collaboration with Biostatistics Develop, review, and validate SDTM and ADaM datasets in accordance with CDISC standards Review specifications and proactively challenge inconsistencies in protocols, SAPs, and dataset definitions Validate program outputs and ensure accuracy, quality, and regulatory compliance Provide oversight and guidance to CRO partners, consolidating and communicating feedback effectively Manage timelines, delivery packages, and milestone commitments Contribute to continuous improvement of programming processes and standards Core Requirements Strong expertise in CDISC standards, including ADaM and SDTM Demonstrated experience reviewing specs and ensuring high-quality, submission-ready deliverables Working experience in LSAF environment Experience validating CRO programming deliverables Ability to operate with increased performance accountability and ownership Strong CRO-facing communication and collaboration skills Proven ability to manage multiple global studies simultaneously Additional Requirements Practical experience with multiple imputation (MI), particularly under Missing at Random (MAR) assumptions Familiarity with the estimands framework (ICH E9 R1) and managing intercurrent events (ICEs) within ADaM domains using various strategies Qualifications Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related field 5+ years of SAS programming experience within pharmaceutical/biotech Strong understanding of statistical methods used in clinical trial analysis Knowledge of Good Programming Practices and GCP Preferred: Experience with R programming

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