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Remote Merck Clinical Trials Jobs (NOW HIRING)

Gilead

Sr Clinical Trials Manager

Foster City, CA · On-site +1

$157K - $203K/yr

Clinical Operations leads the global execution of Phase I-IV clinical trials across therapeutic ... Will not consider fully remote candidates. Responsibilities: * Lead all aspects of assigned ...

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Remote Merck Clinical Trials information

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$20

$43

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How much do remote merck clinical trials jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote merck clinical trials in the United States is $43.09, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $43.03 per hour, depending on experience, location, and employer.

What is a remote Merck clinical trial?

Remote Merck Clinical Trials are research studies conducted by Merck & Co., Inc. that allow participants to take part from their homes or other locations outside of traditional clinical sites. These trials use digital technologies, such as telemedicine, mobile apps, and wearable devices, to monitor participants, collect data, and communicate with study teams. Remote trials aim to make participation more convenient, increase patient diversity, and improve data collection. They may include virtual visits, home delivery of study medications, and remote monitoring of health outcomes. This approach helps expand access to clinical research while maintaining the safety and integrity of the study.

How do remote team members in Merck clinical trials collaborate with on-site staff and ensure seamless trial operations?

Remote team members in Merck Clinical Trials utilize secure digital platforms for communication, data management, and document sharing to stay connected with on-site colleagues. Regular virtual meetings, clear scheduling, and standardized protocols help bridge the distance and maintain alignment on clinical trial milestones. Collaboration tools such as electronic trial master files (eTMF) and project management software are commonly used to track progress and address challenges promptly. This structure enables remote staff to contribute effectively to trial operations, support patient recruitment, and monitor compliance while maintaining efficiency and strong team integration.

What are the key skills and qualifications needed to thrive as a remote clinical trials specialist at Merck?

To excel as a Remote Clinical Trials Specialist at Merck, you generally need a background in life sciences or healthcare, experience in clinical research, and familiarity with Good Clinical Practice (GCP) guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and sometimes certifications like SOCRA or ACRP are commonly required. Strong organizational skills, attention to detail, and effective remote communication are essential soft skills for managing study protocols and collaborating with diverse teams. These competencies are crucial for ensuring regulatory compliance, data integrity, and the efficient coordination of clinical research activities from a remote setting.

What is the difference between Remote Merck Clinical Trials vs Remote Clinical Research Associate?

AspectRemote Merck Clinical TrialsRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonSame as Merck Clinical Trials, often requiring similar degrees and certifications
Work EnvironmentRemote, often within pharmaceutical or biotech companies like MerckRemote, working on clinical trial sites or for research organizations
Employer & Industry UsagePrimarily employed by pharmaceutical companies like Merck, focusing on clinical trial managementEmployed by CROs or pharmaceutical companies, focusing on site monitoring and trial coordination

Both roles involve clinical trial work with similar credentials and work environments. The main difference is that Remote Merck Clinical Trials refers to roles within Merck's clinical trial programs, while Remote Clinical Research Associates typically work across various organizations, focusing on site monitoring and trial coordination.

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Remote Merck Clinical Trials jobs near you
Infographic showing various Remote Merck Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 8% Part Time, and 15% Contract. Highlights an 100% Remote job distribution, with an average salary of $89,619 per year, or $43.1 per hour.

Spanish Bilingual Registered Dietician Clinical Trials Telehealth

IQVIA

Kansas City, MO • Remote

Part-time

Re-posted 8 hours ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 225 rated it services

Job description

Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Missouri

Location: Remote in United States

Job Type: Per Diem

About the Opportunity

Are you a Registered Dietitian seeking a flexible and meaningful role in clinical research?

IQVIA, a global leader in advancing healthcare and clinical research, is seeking experienced Registered Dietitians to support patients participating in clinical trials. This remote role focuses on delivering highquality nutrition assessments and counseling, particularly for individuals living with rare and complex conditions.

This position is ideal for clinicians who want to leverage their expertise in a telehealth environment, contribute to innovative research, and earn supplemental income while maintaining flexibility.

Key Responsibilities

As a Remote Registered Dietitian, you will:

  • Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients with varying disease classifications

  • Provide ongoing dietary counseling and education to patients and their families

  • Deliver nutrition services only to patients in states where you are licensed to practice

  • Support patients enrolled in clinical research studies by monitoring nutritional progress and adherence

  • Maintain accurate, timely, and confidential clinical documentation

  • Participate in virtual team meetings, training sessions, and studyrelated activities

Qualifications

  • Credentialed Registered Dietitian (CDR) with current national registration

  • Active, unrestricted state licensure (except CA, MI, NJ, AZ, VA, and CO)

  • Minimum 1 year of experience providing nutrition planning and patient coaching

  • Minimum 1 year of experience delivering care remotely via telehealth

  • Strong communication and interpersonal skills

  • Experience working with patients with obesity, with or without diabetes (preferred)

  • Experience managing patients on GLP1 therapies (preferred)

  • SpanishEnglish bilingual proficiency is required.

Why Join IQVIA?

  • Flexible per diem schedule that fits your lifestyle

  • Opportunity to gain exposure to clinical trials and researchfocused care

  • Competitive supplemental income

  • Be part of a global organization advancing innovation and patient outcomes

Additional Information

  • This position is not eligible for visa sponsorship.

Ready to make a meaningful impact from anywhere?
Apply today and help support patients while contributing to the future of healthcare research.

#LI-CES and #LI-DNP #LI-HCP #remote

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 athttps://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 is 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

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