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Medical Monitor Jobs in Alabama (NOW HIRING)

Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical monitor, safety physician, or clinical development physician. * Proficiency with CTCAE grading ...

Riverview Regional Medical Center - Gadsden, AL We are seeking a Monitor Technician, sometimes referred to as our Telemetry Monitor Technician (Tech) or Tele Monitor Tech. A Tele Monitor Tech will be ...

Riverview Regional Medical Center - Gadsden, AL We are seeking a Monitor Technician , sometimes referred to as our Telemetry Monitor Technician (Tech) or Tele Monitor Tech. A Tele Monitor Tech will ...

Troubleshoots and resolves issues with monitoring equipment, escalating unresolved problems to Bio-med or IT as directed. * Organizes and tracks monitoring equipment during the shift, ensuring proper ...

Troubleshoots and resolves issues with monitoring equipment, escalating unresolved problems to Bio-med or IT as directed. * Organizes and tracks monitoring equipment during the shift, ensuring proper ...

Troubleshoots and resolves issues with monitoring equipment, escalating unresolved problems to Bio-med or IT as directed. * Organizes and tracks monitoring equipment during the shift, ensuring proper ...

MONITOR I

Columbiana, AL · On-site

$17.25 - $18.50/hr

... such as resident medical problems, disciplinary problems, or new arrivals and any special ... monitors the state of the building. Examples of activities include smelling for marijuana ...

MONITOR I

Columbiana, AL · On-site

$19.75/hr

... such as resident medical problems, disciplinary problems, or new arrivals and any special ... monitors the state of the building. Examples of activities include smelling for marijuana ...

MONITOR I

Columbiana, AL · On-site

$17.25 - $18.50/hr

... such as resident medical problems, disciplinary problems, or new arrivals and any special ... monitors the state of the building. Examples of activities include smelling for marijuana ...

MONITOR I

Columbiana, AL · On-site

$17.25 - $18.50/hr

... such as resident medical problems, disciplinary problems, or new arrivals and any special ... monitors the state of the building. Examples of activities include smelling for marijuana ...

MONITOR I

Columbiana, AL · On-site

$19.75/hr

... such as resident medical problems, disciplinary problems, or new arrivals and any special ... monitors the state of the building. Examples of activities include smelling for marijuana ...

MONITOR I

Columbiana, AL · On-site

$17.25 - $18.50/hr

... such as resident medical problems, disciplinary problems, or new arrivals and any special ... monitors the state of the building. Examples of activities include smelling for marijuana ...

The Women's Medical Center provides comprehensive women's services through all stages of life ... Responsibilities Monitors and reviews patient information to determine baseline cardiac rhythm.

The Women's Medical Center provides comprehensive women's services through all stages of life ... Responsibilities • Monitors and reviews patient information to determine baseline cardiac rhythm ...

The Women's Medical Center provides comprehensive women's services through all stages of life ... Responsibilities • Monitors and reviews patient information to determine baseline cardiac rhythm ...

Showing results 21-40

Medical Monitor information

See Alabama salary details

$19K

$83.9K

$161.3K

How much do medical monitor jobs pay per year?

As of Aug 11, 2026, the average yearly pay for medical monitor in Alabama is $83,891.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,600.00 and $76,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the medical monitor position, and why are they important?

To thrive as a Medical Monitor, you need a deep understanding of clinical research, medical evaluation, and regulatory compliance, typically supported by a medical degree (MD or equivalent) and clinical experience. Familiarity with clinical trial management systems (CTMS), safety databases, and Good Clinical Practice (GCP) certification is essential. Excellent communication, analytical thinking, and problem-solving skills help you clearly communicate findings and collaborate with cross-functional teams. These competencies are vital to ensure participant safety, data integrity, and the smooth conduct of clinical trials.

What is a medical monitor?

A Medical Monitor is a physician responsible for ensuring the safety and integrity of clinical trials. They provide medical oversight by reviewing patient data, assessing adverse events, and ensuring compliance with regulatory guidelines. Medical Monitors work closely with clinical teams, investigators, and regulatory agencies to support the study's progress and ethical conduct. Their expertise helps ensure that trials meet safety standards while gathering reliable data for drug development.

What are the typical daily responsibilities of a medical monitor in a clinical research setting?

As a Medical Monitor, your daily responsibilities often include reviewing adverse event reports, monitoring patient safety data, and providing medical input during clinical trial meetings. You will interpret clinical data, ensure protocol adherence, and address any medical queries from site staff or sponsors. Additionally, you collaborate closely with clinical operations, safety, and regulatory teams to ensure trials are conducted safely and efficiently. This role requires ongoing communication with investigators and the ability to rapidly assess and respond to potential safety concerns.

Infographic showing various Medical Monitor job openings in Alabama as of August 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,891 per year, or $40.3 per hour.

Hematologist / Oncologist

micro1 AI

Montgomery, AL • 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.