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Study Com Jobs in Alaska (NOW HIRING)

KA Recruiting Inc.

Radiology Manager in Alaska

Angoon, AK · On-site

$44 - $59.75/hr

The Radiology Manager oversees activities of Radiology program; tracks radiology studies coming ... To apply, email your resume to leah@ka-recruiting.com/call or text 617-746-2751! You can also ...

GovernmentJobs.com

Eligibility Technician 2

Anchorage, AK · On-site

$47K - $61K/yr

... Study; therefore, the title and/or pay range currently assigned may be subject to change upon ... For information on allowing emails from the 'governmentjobs.com' domain, visit the Lost Password ...

palmerprojectak

Senior Geologist

Palmer, AK · On-site

$80 - $120/hr

Interested candidates can send a detailed resume and cover letter to careers@constantinemetals.com ... Supervise on-the-ground aspects of the company drill programs and related geoscience studies ...

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Showing results 1-20

All JobsStudy Com JobsStudy Com Jobs in Alaska

Study Com information

See Alaska salary details

$23.7K

$134.9K

$221.9K

How much do study com jobs pay per year?

As of Aug 16, 2026, the average yearly pay for study com in Alaska is $134,931.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,500.00 and $169,100.00 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 job categories do people searching Study Com jobs in Alaska look for?

The top searched job categories for Study Com jobs in Alaska are:

Study Com jobs near you
Infographic showing various Study Com job openings in Alaska as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 27% Part Time, 1% Temporary, and 4% Contract. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $134,931 per year, or $64.9 per hour.

Nephrologist (Clinical Trails) - Part-time - Anchorage, AK

ProTouch Staffing

Anchorage, AK • On-site

Other

Re-posted 17 days ago

Job description

Clinical Trial Nephrologist - Anchorage, AK

Job location: Anchorage, AK

Job type: Part-time

Shift: Flexible

Job Description:

We are seeking a board-certified Nephrologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in our current and upcoming clinical trials. The Dermatologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with the research team to maintain high-quality trial execution.

Key Responsibilities:

  • Serve as PI or Sub-I in assigned clinical trials.

  • Conduct medical evaluations and assess participant eligibility.

  • Monitor patient safety, adverse events, and treatment outcomes.

  • Review and sign study-related documentation per protocol and regulations.

  • Collaborate with study coordinators, nurses, and other research staff.

  • Attend protocol training and ensure adherence to Good Clinical Practice (GCP).

Qualifications:

  • MD or DO with an active CA medical license.

  • Board-certified in Nephrology.

  • Interest in clinical research (prior experience preferred; training provided if needed).

  • Strong communication, teamwork, and organizational skills.

Benefits:

  • Flexible schedule: 0-8 hours/week.

  • Professional growth opportunities in clinical research.

  • Contribute to advancing dermatology treatments and patient outcomes.

For more information, please reach out to Dheeraj Mohan: at (469) 430-0547 or by Email: at dheeraj.mohan@protouchstaffing.com.

Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

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