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Clinical Study Jobs in Virginia (NOW HIRING)

micro1 AI

Medical Writing Manager

Norfolk, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Writing Manager

Suffolk, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Alexandria, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Virginia Beach, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Writing Manager

Chesapeake, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Newport News, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Chesapeake, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Roanoke, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Writing Manager

Alexandria, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Norfolk, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Writing Manager

Virginia Beach, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Writing Manager

Richmond, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Billing Specialist

Hampton, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

micro1 AI

Medical Writing Manager

Roanoke, VA · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development. * Apply expert judgment to assess ...

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Showing results 41-60

All JobsClinical Study JobsClinical Study Jobs in Virginia

Clinical Study information

See Virginia salary details

$21.8K

$124.2K

$204.2K

How much do clinical study jobs pay per year?

As of Aug 10, 2026, the average yearly pay for clinical study 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 a clinical study?

Clinical studies are research investigations conducted with human volunteers to evaluate the safety, effectiveness, and side effects of medical treatments, drugs, devices, or interventions. These studies follow strict scientific and ethical guidelines and are usually carried out in several phases before a treatment can be approved for widespread use. Clinical studies help determine whether new approaches to prevention, diagnosis, or therapy are safe and effective for people. Participation in clinical studies is voluntary and can contribute to advancements in medical science.

What are some common challenges faced when managing multiple clinical studies simultaneously?

Professionals involved in clinical studies often juggle several projects at once, which can present challenges such as balancing competing timelines, ensuring regulatory compliance across studies, and coordinating with diverse teams. Effective project management, clear communication, and strong organizational skills are key to addressing these challenges. Utilizing project management tools and maintaining detailed documentation can help keep studies on track and reduce the risk of errors or delays.

Do clinical studies pay well?

Clinical study roles, such as clinical research coordinators or assistants, typically offer moderate pay that varies by experience, location, and employer. Entry-level positions may start at lower wages, while experienced professionals or those with specialized skills can earn higher salaries, especially when working on complex or long-term studies.

What is the difference between Clinical Study vs Clinical Research Coordinator?

AspectClinical StudyClinical Research Coordinator
CredentialsOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are advantageous
Work EnvironmentConducted in hospitals, clinics, or research facilities; involves direct patient interaction and data collectionWorks in research sites, hospitals, or clinics; manages study logistics and coordinates between teams
Employer & IndustryPharmaceutical companies, academic institutions, CROsResearch institutions, hospitals, pharmaceutical companies

While both roles are integral to clinical research, a Clinical Study typically refers to the overall research process or specific studies, whereas a Clinical Research Coordinator is a professional who manages and oversees the day-to-day operations of clinical trials. Understanding these distinctions helps in choosing the right career path or job search focus.

What jobs are there in clinical studies?

Jobs in clinical studies include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research facility, hospital, or pharmaceutical company, with schedules varying from full-time to part-time depending on the role.

What are the key skills and qualifications needed to thrive as a clinical study coordinator?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory guidelines like GCP, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as CCRC or CCRA is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating multiple tasks and interacting with diverse stakeholders. These skills ensure compliance, accurate data collection, and smooth trial operations, which are vital for the integrity and success of clinical studies.
What are the most commonly searched types of Clinical Study jobs in Virginia? The most popular types of Clinical Study jobs in Virginia are:
What cities in Virginia are hiring for Clinical Study jobs? Cities in Virginia with the most Clinical Study job openings:
Clinical Study jobs near you
Infographic showing various Clinical Study job openings in Virginia as of August 2026, with employment types broken down into 2% As Needed, 69% Full Time, 21% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $124,215 per year, or $59.7 per hour.

Medical Writing Manager

micro1 AI

Norfolk, VA • Remote

$50 - $80/hr

Part-time

Posted 6 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply