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Study Com Jobs in Remote, OR (NOW HIRING)

IT ENGAGEMENTS INC

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CGM Statistician (Contract Role)

OR · On-site

$65 - $70/hr

Perform statistical analysis for Continuous Glucose Monitoring (CGM) studies. * Develop statistical ... Regards, vinaya [at] Itengagements [dot] com

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IT ENGAGEMENTS INC

Be Seen First

CGM Statistician (Contract Role)

OR · On-site

$65 - $70/hr

Perform statistical analysis for Continuous Glucose Monitoring (CGM) studies. * Develop statistical ... Regards, vinaya [at] Itengagements [dot] com

New

Kemira

Coordinator, Sales, P&HS, NA Corporate Accounts

OR · Remote

$67K - $84K/yr

Learn more about Kemira at www.kemira.com/careers. We are now seeking a Sales Coordinator to join ... Bachelor's degree or equivalent in a relevant field of study such as Business Administration ...

Kemira

Coordinator, Sales, P&HS, NA Corporate Accounts

OR · On-site +1

$67K - $84K/yr

Learn more about Kemira at www.kemira.com/careers. We are now seeking a Sales Coordinator to join ... Bachelor's degree or equivalent in a relevant field of study such as Business Administration ...

KurzSolutions

Primary Care Physician

Roseburg, OR · On-site

... tests, imaging studies (e.g., X-rays), and other diagnostic procedures as needed. * Analyze ... market. www.kurzsolutions.com KurzSolutions is an Equal Opportunity Employer. We do not ...

All JobsStudy Com JobsStudy Com Jobs in Remote, OR

Study Com information

See Remote, OR salary details

$22K

$125.2K

$205.8K

How much do study com jobs pay per year?

As of Sep 8, 2026, the average yearly pay for study com in Remote, OR is $125,167.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,900.00 and $156,800.00 per year, depending on experience, location, and employer.

What is a study com?

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 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 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 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 popular job titles related to Study Com jobs in Remote, OR?

For Study Com jobs in Remote, OR, the most frequently searched job titles are:

What cities near Remote, OR are hiring for Study Com jobs?

Cities near Remote, OR with the most Study Com job openings:

Study Com jobs near you
Infographic showing various Study Com job openings in Remote, OR as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, and 6% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $125,167 per year, or $60.2 per hour.

CGM Statistician (Contract Role)

IT ENGAGEMENTS INC

OR • On-site

$65 - $70/hr

Contractor

Posted 3 days ago

New

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Job description

Greetings from IT Engagements



Job Title: CGM Statistician (Contract Role)
Work Location: Remote


Responsibilities:

  • Perform statistical analysis for Continuous Glucose Monitoring (CGM) studies.
  • Develop statistical analysis plans and statistical programming specifications.
  • Analyze CGM and clinical trial data and interpret statistical results.
  • Support study reports, tables, listings, and figures.
  • Collaborate with clinical, data management, and programming teams.


Requirements:

  • Experience as a Statistician/Biostatistician in clinical research.
  • Experience working with Continuous Glucose Monitoring (CGM) data.
  • Strong SAS programming and statistical analysis skills.
  • Experience with clinical trial data and statistical methodologies.


Regards,

vinaya [at] Itengagements [dot] com