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Medical Monitoring Associate Jobs (NOW HIRING)

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... Medical Monitoring: * Primarily serves as Global and /or Regional Medical Advisor on assigned ...

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... Medical Monitoring: * Primarily serves as Global and /or Regional Medical Advisor on assigned ...

The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... Medical Monitoring: * Primarily serves as Global and /or Regional Medical Advisor on assigned ...

Alarm Monitoring Representative

Irving, TX · On-site

$34K - $39K/yr

We have exceptional career opportunities for On-Site Monitoring Associates. This is an on-site ... Medical, Dental, Vision, 401(k) with employer matching * Paid vacation time (We all need to ...

$16.80 - $21.83/hr

Assists with training new staff on medical monitoring systems. Qualifications Education * High School Diploma or GED, (Required) * Associates Degree, (Preferred) Experience * 1 year Monitor ...

New

$16.80 - $21.83/hr

Assists with training new staff on medical monitoring systems. Qualifications Education * High School Diploma or GED, (Required) * Associates Degree, (Preferred) Experience * 1 year Monitor ...

$16.80 - $21.83/hr

Assists with training new staff on medical monitoring systems. Qualifications Education * High School Diploma or GED, (Required) * Associates Degree, (Preferred) Experience * 1 year Monitor ...

Mentor and coach safety associates and non-medical team members. Develop and deliver training ... Minimum of 3 years of experience in clinical research or medical monitoring, preferably with a ...

Showing results 41-60

Medical Monitoring Associate information

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$24K

$58.4K

$135K

How much do medical monitoring associate jobs pay per year?

As of Sep 13, 2026, the average yearly pay for medical monitoring associate in the United States is $58,439.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,500.00 and $69,500.00 per year, depending on experience, location, and employer.

What is a medical monitoring associate?

Medical Monitoring Associates are professionals who support clinical trials by overseeing the safety of study participants and ensuring that medical data is accurately collected and reported. They work closely with medical monitors, investigators, and clinical research teams to review adverse events, monitor compliance with study protocols, and help resolve medical queries. Their role is vital in maintaining the integrity of clinical trials and ensuring participant safety throughout the research process.

How does a medical monitoring associate typically collaborate with clinical research teams during a study?

Medical Monitoring Associates play a crucial role in ensuring patient safety and data integrity throughout clinical trials. They work closely with clinical research teams by reviewing safety reports, tracking adverse events, and communicating findings to investigators and study sponsors. Collaboration often involves participating in regular team meetings, providing feedback on protocol adherence, and assisting with the preparation of study documentation. This close teamwork ensures that the trial runs smoothly and adheres to regulatory guidelines.

What are the key skills and qualifications needed to thrive as a medical monitoring associate, and why are they important?

To thrive as a Medical Monitoring Associate, you need a solid background in life sciences or nursing, familiarity with clinical trial protocols, and often a relevant degree or certification. Proficiency in clinical data management systems, safety databases, and regulatory compliance tools is typically required. Attention to detail, strong analytical skills, and effective communication are essential soft skills that help ensure accurate medical oversight and teamwork. These competencies are vital to ensure patient safety, regulatory adherence, and the overall integrity of clinical trials.

What cities are hiring for Medical Monitoring Associate jobs?

Cities with the most Medical Monitoring Associate job openings:

What are the most commonly searched types of Medical Monitoring jobs?

The most popular types of Medical Monitoring jobs are:

What are popular job titles related to Medical Monitoring Associate jobs?

For Medical Monitoring Associate jobs, the most frequently searched job titles are:

Infographic showing various Medical Monitoring Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $58,439 per year, or $28.1 per hour.

Medical Director, Cardiology

Durham, NC • On-site

IQVIA, Inc.
Health Care and Social Assistance • 10K+ employees

Full-time

Re-posted 5 days ago


Key responsibilities

  • Provide medical, clinical, and scientific advisory expertise to all IQVIA divisions as requested.

  • Serve as a medical expert during project delivery lifecycle, including medical monitoring and review of trial-related documentation.

  • Participate in business development activities by providing therapeutic and medical expertise, including developing medically sound delivery strategies and reviewing proposals.


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz


Job description

Job Posting Title- Medical Director, Cardiology
Location: Home-based in the U.S.
Job Overview:
The Associate Medical Director / Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities as requested.
Essential Functions
The role includes predominantly Medical Monitoring responsibilities with therapeutic and medical expertise to Business Development activities as requested.
Medical Monitoring:
  • Primarily serves as Global and /or Regional Medical Advisor on assigned projects.
  • Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.
  • Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
  • Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
  • Provides therapeutic area/indication training for the project clinical team.
  • Attends and presents at Investigator Meetings.
  • Performs review and clarification of trial-related Adverse Events (AEs).
  • May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
  • May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
  • May perform medical review of adverse event coding.
  • Performs review of the Clinical Study Report (CSR) and patient narratives.
  • Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
  • Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.

Medical Strategy:
  • Provides expert advice on the development of medically sounded delivery strategies for small to large and/or complex multi-region studies in partnership with sales and other functions responsible for business development activities.
  • Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring.
  • Provides medical and scientific advice to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
  • Attend and present at bid defense preparation and bid defense meetings, as required.
  • Participates in strategic business development activities including presentations to prospective clients.
  • Maintains awareness of industry development and may author related publications.
  • Requires periodic regional and international travel.

Qualifications
  • Board certification in Cardiology.
  • Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to the specific therapeutic area, plus a minimum of 5 years' experience in clinical medicine post residency period.
  • Typically requires 5 - 7 years of prior relevant experience in the requested medical specialty area; In addition, previous clinical research experience as an investigator or in the Pharma, CRO, or Biotech industry is required.
  • Experience in Clinical Development (Phase I -IV)
  • Prior experience in cardiology with exposure to metabolic disease indications is preferred.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  • Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).
  • Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area.
  • Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
  • Current or prior license to practice medicine.

#LI-Remote
#LI-NITINMAHAJAN
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $154,900.00 - $431,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US