ZipRecruiter

Log In

2

Remote Case Study Writer Jobs in Mississippi (NOW HIRING)

micro1 AI

Hematologist / Oncologist

Jackson, MS · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Provide structured, guideline-based written rationales that clearly explain the validity or ...

micro1 AI

Clinician (Oncology / Hematology)

Jackson, MS · Remote

$160 - $200/hr

Remote micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer's project ... Provide structured, guideline-based written rationales that clearly explain the validity or ...

Varsity Tutors

Arabic Tutor

Starkville, MS · Remote

$18 - $40/hr

Deep knowledge of Arabic script, root-pattern morphology, noun and verb conjugation, case marking ... written MSA with spoken dialect exposure and relates Arabic language to Islamic studies, Middle ...

Vital Care Infusion Services

Billing Associate

Meridian, MS · On-site +1

$18.92 - $20/hr

A remote work opportunity is available after 120 days of training and support, once consistent ... Document case activity, communications, and correspondence in CareTend to ensure completeness and ...

VieMed

Respiratory Sales Representative

Vicksburg, MS · On-site +1

In recent random studies of our patient population, we have shown a 30-day COPD re-admission rate ... Pulmonologist, Hospitalist, Critical Care Physicians, Case Managers, and Social Workers. Essential ...

previous page

Showing results 21-36

All JobsCase Study Writer JobsRemote Case Study Writer JobsRemote Case Study Writer Jobs in Mississippi

Remote Case Study Writer information

What is the difference between Remote Case Study Writer vs Remote Content Writer?

AspectRemote Case Study WriterRemote Content Writer
CredentialsWriting experience, industry knowledge, sometimes marketing or business backgroundGeneral writing skills, SEO knowledge, content marketing experience
Work EnvironmentFreelance or remote, often project-based, working with businesses or agenciesRemote, creating various content types like blogs, articles, social media posts
Industry UsageCommon in consulting, B2B, tech, healthcare sectorsUsed across multiple industries including marketing, media, education

The main difference is that Remote Case Study Writers focus on creating detailed, industry-specific case studies that showcase client success stories, requiring specialized knowledge. Remote Content Writers produce a broader range of content types for various purposes. Both roles are remote and require strong writing skills, but their focus and output differ significantly.

What does a remote case study writer do?

A remote case study writer creates detailed reports that analyze real-world business situations, highlighting challenges, solutions, and results. They research, interview clients or stakeholders, and craft clear, well-structured narratives often using writing and editing skills, typically working independently on flexible schedules.
What are popular job titles related to Remote Case Study Writer jobs in Mississippi? For Remote Case Study Writer jobs in Mississippi, the most frequently searched job titles are:
What job categories do people searching Remote Case Study Writer jobs in Mississippi look for? The top searched job categories for Remote Case Study Writer jobs in Mississippi are:
What cities in Mississippi are hiring for Remote Case Study Writer jobs? Cities in Mississippi with the most Remote Case Study Writer job openings:
Remote Case Study Writer jobs near you

Hematologist / Oncologist

micro1 AI

Jackson, MS • Remote

$160 - $200/hr

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

Role Title: Clinician (Oncology / Hematology)


Role Type: Contractor


Location: Remote


micro1 is engaging Clinician (Oncology / Hematology)s to contribute to a customer’s project at the forefront of AI in healthcare. 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 evaluation tasks that require nuanced clinical judgment, leveraging Clinical Study Reports, periodic safety reports, and regulatory correspondence in oncology and haematology.
  2. Assess the clinical defensibility of efficacy and safety conclusions, ensuring endpoints and effect sizes reflect true clinical significance.
  3. Apply advanced judgment to dose escalation, dose-limiting toxicity, modifications, adverse event grading and attribution, and the coherence of patient narratives.
  4. Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events, and the realism of described management strategies.
  5. Identify and flag content that is clinically implausible or internally inconsistent, distinguishing these from legitimate clinical variation.
  6. Provide structured, guideline-based written rationales that clearly explain the validity or limitations of clinical interpretations for a non-clinical audience.


Preferred Qualifications

  1. Specialist registration or board certification in medical oncology and/or haematology, with 5+ years of post-training clinical experience.
  2. Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical monitor, safety physician, or clinical development physician.
  3. Proficiency with CTCAE grading, relevant response criteria (RECIST, Lugano, IMWG, IWCLL, ELN), and outcome endpoints (ORR, DoR, PFS, OS, MRD).
  4. Hands-on experience with trial documents such as protocols, investigator brochures, CSRs, safety narratives, or DSMB/IDMC materials.
  5. Demonstrated excellence in written communication, with clear, structured explanations of clinical reasoning tailored for non-clinical readers.
  6. Previous roles in medical monitoring or as medical director on oncology or haematology programmes, and committee participation (IDMC, DSMB, adjudication, or independent review committees).
  7. Peer-reviewed publication record or authorship on clinical trial manuscripts, with any exposure to AI-assisted clinical review tools seen as a plus.

Apply