ZipRecruiter

Log In

1

Study Com Jobs in Virginia (NOW HIRING)

Iteris

Traffic Safety Engineer

Salem, VA · On-site

$97K - $108K/yr

Support engineering safety study program for VDOT Salem District in Salem, VA * Perform safety ... For more information, visit Iteris' website at www.iteris.com. The Almaviva Group designs ...

AbbVie

Clinical Research Associate II

Richmond, VA · On-site

For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn ... Advanced level of competency connecting the study protocol, scientific principles and clinical ...

AbbVie

Clinical Research Associate II

Richmond, VA · On-site +1

$78K/yr

For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn ... Advanced level of competency connecting the study protocol, scientific principles and clinical ...

AbbVie

Clinical Research Associate II

Richmond, VA · On-site

For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn ... Advanced level of competency connecting the study protocol, scientific principles and clinical ...

GovernmentJobs.com

Fire Medic II (Advanced- EMT)

Windsor, VA · On-site

$16.75 - $22.25/hr

... studies street and road patterns and networks of the County in order that future runs may be made with minimum difficulty and delay. * Inspects and tests fire apparatus and ambulances and their ...

previous page

Showing results 41-60

All JobsStudy Com JobsStudy Com Jobs in Virginia

Study Com information

See Virginia salary details

$21.8K

$124.2K

$204.2K

How much do study com jobs pay per year?

As of Aug 8, 2026, the average yearly pay for study com in Virginia is $124,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,300.00 and $155,700.00 per year, depending on experience, location, and employer.

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.

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 popular job titles related to Study Com jobs in Virginia? For Study Com jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Study Com jobs in Virginia look for? The top searched job categories for Study Com jobs in Virginia are:
What cities in Virginia are hiring for Study Com jobs? Cities in Virginia with the most Study Com job openings:
Study Com jobs near you
Infographic showing various Study Com job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 21% Part Time, 1% Temporary, and 5% Contract. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $124,215 per year, or $59.7 per hour.

Clinical Protocol Developer

Culmen International LLC

Portsmouth, VA

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 28 days ago

Job description

Culmen International, LLC is hiring a Clinical Protocol Developer to assist the Naval Medical Center in Portsmouth, VA. 

This position will support the Department Head of CID and is accountable for research related matters to the PIs of each research protocol. Provide support to the Department Head of CID and the PI of each protocol in accordance with written policies and procedures as set forth in Title 21 of the Code of Federal Regulations, NMCP and Bureau of Medicine & Surgery (BUMED) instructions

This position is onsite in Portsmouth, VA. 


  • Assist physicians/scientists in developing, writing, and producing human and animal research protocols in support of the military medicine research programs 
  • Assist with the preparation of investigator-initiated trials to include coordination of the protocol submission, submission of amendments and regulatory compliance reports, and the development of presentations and/or publications 
  • Assist with preparing informed consent statements and other study-related research documents 
  • Conduct literature reviews and draft scientific and technical documents 
  • Contribute to the preparation and modification of internal study budgets 
  • Assist with ensuring PI-initiated protocols contain quality research design, and meet DOD standards for ethics and compliance 
  • Assist the PI with addressing Scientific Review Committee (SRC), Institutional Review Board (IRB), and other committee queries 
  • Attend and assist with the planning of committee meetings for disease-specific working groups to facilitate research development 
  • Assist with administering the study development tracking system and updating protocol details and development events in eIRB system 
  • Work with the data management team, clinical operations team, and other research collaborators in transitioning projects from the development team to the operations team that incorporates the clinical details needed to treat patients and the research elements to answer study questions 
  • Assist the clinical research coordinators in the development of specimen submission.  
  • Assist the research and statistical data coordinators, database developers, and database administrators in study database development and data monitoring planning 
  • Assist with collecting information on reported problems regarding consistency and/or clarity in open protocols. 
  • Assist with initial and follow-on updates of study registration on clinicaltrials.gov, including facilitation of Quality Assurance (QA)  
  • Participate in the collection of data, supporting both human and animal protocols. 
  • Provide education and training to researchers and staff on protocol development  

  • Bachelor's Degree
  • 5 Years of Clinical Research Experience
  • Ability to obtain a Secret Clearance

Culmen International is committed to enhancing international safety and security, strengthening homeland defense, advancing humanitarian missions, and optimizing government operations. With experience in over 150 countries, Culmen supports our clients to accomplish critical missions in challenging environments.

  • Exceptional Medical/Dental/Vision Insurance, premiums for employees are 100% paid by Culmen, and dependent coverage is available at a nominal rate (including same or opposite sex domestic partners) 

  • 401k – Vested immediately and 4% match
  • Life insurance and disability paid by the company
  • Supplemental Insurance Available
  • Opportunities for Training and Continuing Education
  • 12 Paid Holidays

To learn more about Culmen International, please visit www.culmen.com

At Culmen International, we are committed to creating and sustaining a workplace that upholds the principles of Equal Employment Opportunity (EEO). We believe in the importance of fair treatment and equal access to opportunities for all employees and applicants.  Our commitment to these principles is unwavering across all our operations worldwide.

The determination of compensation at Culmen International, LLC is based on various factors such as location, the individual's unique combination of education, knowledge, skills, competencies, clearance level, experience, internal equity, contract-specific affordability, and organizational requirements. 

Apply