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Remote Study Abroad Manager Jobs in Kansas (NOW HIRING)

micro1 AI

Medical Billing Specialist

Topeka, KS · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Alpine Intel

Fire Investigator

Topeka, KS · Remote

They will do all the required studies and all other work necessary to determine the cause and ... Remote Schedule * Competitive Compensation Package * Bonus Opportunity * Career Growth * A Diverse ...

Syneoshealth

... line management; technical and therapeutic area training; peer recognition and total rewards ... US or Canada (Hybrid/Remote) Position Overview The Research Associate/Senior Research Associate ...

Veristat

The Principal Medical Writer works under the direction of Medical Writing management and ... Provide coaching to junior staff for study level documents as well as submission level documents ...

Olsson

Civil Design Manager - Site Design

Topeka, KS · On-site +1

May assist in the preparation of project studies by completing drawings, sketching, or acquiring ... This role offers flexible work options, including remote and hybrid opportunities, to accommodate ...

Olsson

Civil Design Manager - Site Design

Salina, KS · On-site +1

May assist in the preparation of project studies by completing drawings, sketching, or acquiring ... This role offers flexible work options, including remote and hybrid opportunities, to accommodate ...

Olsson

Civil Design Manager - Site Design

Wichita, KS · On-site +1

May assist in the preparation of project studies by completing drawings, sketching, or acquiring ... This role offers flexible work options, including remote and hybrid opportunities, to accommodate ...

Olsson

Civil Design Manager - Site Design

Wichita, KS · On-site +1

May assist in the preparation of project studies by completing drawings, sketching, or acquiring ... This role offers flexible work options, including remote and hybrid opportunities, to accommodate ...

Veristat

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...

Veristat

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...

Veristat

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Experience in the development of clinical documents such as Clinical Study Reports, Investigator ...

Actalent

Wetland Scientist

Leawood, KS · On-site +1

$73K - $95K/yr

Perform independent field studies, including botanical surveys, natural community mapping, wildlife ... remote or rugged environments. * Task or project management experience, including planning ...

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All JobsStudy Abroad JobsRemote Study Abroad Manager JobsRemote Study Abroad Manager Jobs in Kansas

Remote Study Abroad Manager information

What is the difference between Remote Study Abroad Manager vs Remote Education Coordinator?

AspectRemote Study Abroad ManagerRemote Education Coordinator
Required CredentialsBachelor's degree, experience in international educationBachelor's degree, background in education or administration
Work EnvironmentOversees study abroad programs, liaises with partner institutionsSupports educational programs, manages student communications
Employer & Industry UsageUniversities, study abroad agenciesEducational institutions, online learning platforms
Search & Comparison IntentFocuses on international program managementCenters on student support and program coordination

The Remote Study Abroad Manager primarily manages international study programs and liaises with partner institutions, requiring experience in international education. In contrast, the Remote Education Coordinator focuses on supporting educational programs and student communications. Both roles often require similar educational backgrounds but differ in their core responsibilities and work environments.

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Remote Study Abroad Manager jobs near you

Medical Billing Specialist

micro1 AI

Topeka, KS • Remote

$50 - $80/hr

Part-time

Posted 16 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