ZipRecruiter

Log In

2

Remote Apple Clinical Research Jobs (NOW HIRING)

Trice Healthcare

Clinical Research Informatician

Remote Duration: Direct Hire FTE Must Have's: * Bachelor's Degree in Health Information Management ... Clinical Research * Clinical Informatics * Information Technology and/or Academic Healthcare ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

next page

Showing results 1-20

All Jobsremote JobsHealthcare JobsMedical Research JobsClinical Researcher JobsRemote Apple Clinical Research Jobs

Remote Apple Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do remote apple clinical research jobs pay per year?

As of Aug 26, 2026, the average yearly pay for remote apple clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is remote Apple Clinical Research?

A Remote Apple Clinical Research job involves conducting or supporting clinical research activities for Apple, often related to the development and validation of health technologies and products like the Apple Watch or Health app. Professionals in these roles may design studies, collect and analyze health data, and collaborate with medical and engineering teams, all while working from a remote location. The goal is to advance innovative digital health solutions by ensuring they are safe, effective, and meet regulatory standards. These positions often require backgrounds in clinical research, data analysis, or biomedical sciences, and familiarity with digital health technologies.

What are the key skills and qualifications needed to thrive in remote Apple Clinical Research?

To excel in Remote Apple Clinical Research, you generally need a background in life sciences or healthcare, experience in clinical research, and familiarity with regulatory guidelines like GCP. Proficiency with electronic data capture (EDC) systems, remote monitoring tools, and Apple Health technologies is typically required. Strong attention to detail, analytical thinking, and effective communication are vital soft skills for coordinating studies and collaborating remotely. These competencies ensure rigorous data integrity, regulatory compliance, and effective teamwork in a distributed research environment.

What are some common challenges faced by professionals in remote Apple Clinical Research roles, and how can they be addressed?

Professionals in remote Apple Clinical Research positions often face challenges related to coordinating with cross-functional teams across different time zones and ensuring clear communication without in-person meetings. Managing sensitive clinical data securely while working remotely also requires strict adherence to data privacy protocols. To address these challenges, it's important to establish regular virtual check-ins, use secure collaboration platforms, and maintain thorough documentation of research activities. Proactively communicating with team members and participating in virtual training sessions can further help ensure project goals are met efficiently.

What is the difference between Remote Apple Clinical Research vs Remote Apple Clinical Trial Coordinator?

AspectRemote Apple Clinical ResearchRemote Apple Clinical Trial Coordinator
CredentialsTypically requires clinical research certifications, life sciences degreeRequires similar certifications, often with additional trial management training
Work EnvironmentRemote, primarily data analysis, protocol developmentRemote, coordinating trial activities, communication with sites
Employer & IndustryPharmaceutical/biotech companies, research institutionsPharmaceutical companies, clinical research organizations

Remote Apple Clinical Research involves designing and analyzing clinical studies, while Remote Apple Clinical Trial Coordinators manage trial logistics and site communication. Both roles require similar certifications and are remote, but they focus on different aspects of clinical research processes.

More about Remote Apple Clinical Research jobs

What cities are hiring for Remote Apple Clinical Research jobs?

Cities with the most Remote Apple Clinical Research job openings:

What are the most commonly searched types of Apple Clinical Research jobs?

The most popular types of Apple Clinical Research jobs are:

What states have the most Remote Apple Clinical Research jobs?

States with the most job openings for Remote Apple Clinical Research jobs include:

What job categories do people searching Remote Apple Clinical Research jobs look for?

The top searched job categories for Remote Apple Clinical Research jobs are:

Remote Apple Clinical Research jobs near you
Infographic showing various Remote Apple Clinical Research job openings in the United States as of August 2026, with employment types broken down into 5% Internship, 90% Full Time, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 4 days ago. Applications are no longer accepted.

Job description

This is a remote position.

Position Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support the coordination and administration of clinical research studies while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process.

This position is ideal for someone with excellent organizational skills, strong attention to detail, and an interest in contributing to clinical research in a remote environment.

Essential Responsibilities
  • Assist with the day-to-day management of assigned clinical studies.
  • Maintain investigator site files, regulatory binders, and essential study documents.
  • Prepare, review, and file research documentation in accordance with study requirements.
  • Support participant scheduling and study visit coordination.
  • Enter, verify, and reconcile clinical data within electronic research systems.
  • Monitor study timelines and assist with tracking project deliverables.
  • Communicate effectively with investigators, sponsors, study participants, and internal research teams.
  • Identify and escalate documentation discrepancies or protocol deviations when appropriate.
  • Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements.
  • Perform additional administrative and research support duties as assigned.


RequirementsQualifications
Required
  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related discipline, or equivalent healthcare experience.
  • Strong organizational and problem-solving abilities.
  • Excellent verbal and written communication skills.
  • High level of accuracy and attention to detail.
  • Proficiency with Microsoft Office and web-based software applications.
  • Ability to manage multiple priorities while working independently in a remote setting.
Preferred
  • Previous experience supporting clinical research or healthcare operations.
  • Familiarity with ICH-GCP guidelines and FDA regulations.
  • Experience using Electronic Data Capture (EDC), CTMS, or eTMF systems.
  • Knowledge of clinical trial documentation and research workflows.
Work Schedule
  • Full-time
  • Monday through Friday
  • Standard business hours


BenefitsBenefits
  • Competitive salary
  • Comprehensive medical, dental, and vision coverage
  • 401(k) with employer contribution
  • Paid time off and company holidays
  • Remote work environment
  • Professional development and career advancement opportunities