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Remote Observational Research Jobs (NOW HIRING)

Vitalief

Clinical Research Coordinator

Newark, NJ · Remote

$40 - $45/hr

Remote Flexibility: Most study coordination activities can be performed remotely, including patient ... Minimum of 2 years of clinical research coordination experience supporting observational and/or ...

Slipstream IT

Statistical Analytical Programmer

PA · On-site +1

... observational research and epidemiologic methods to support regulatory and scientific projects ... Able to work independently in a remote environment and manage timelines effectively. Preferred ...

Slipstream IT

Statistical Analytical Programmer

PA · Remote

... observational research and epidemiologic methods to support regulatory and scientific projects ... Able to work independently in a remote environment and manage timelines effectively. Preferred ...

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How much do remote observational research jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for remote observational research in the United States is $22.22, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $23.80 per hour, depending on experience, location, and employer.

What is remote observational research?

Remote observational research is a method where researchers study participants or environments without being physically present. This is often done using digital tools such as video calls, remote sensors, or online platforms, allowing data collection from a distance. The approach is valuable for reaching wider or hard-to-access populations and can be more convenient and cost-effective. Remote observational research is commonly used in fields like healthcare, education, and social sciences to observe behaviors, interactions, or outcomes in real time or asynchronously.

What are the key skills and qualifications needed to thrive as a remote observational researcher?

To thrive as a Remote Observational Researcher, you need strong analytical skills, attention to detail, and a background in research methods, often supported by a degree in psychology, sociology, public health, or a related field. Familiarity with data collection tools, survey software, statistical analysis programs (such as SPSS or R), and remote collaboration platforms is typically required. Excellent communication, self-motivation, and organizational skills help you effectively manage independent work and present findings clearly. These capabilities are essential for ensuring accurate data collection and analysis, enabling impactful insights in a remote research setting.

What are some common challenges faced by professionals in remote observational research and how can they be addressed?

Professionals in Remote Observational Research often face challenges such as maintaining data quality across diverse and decentralized study sites, ensuring participant compliance, and managing technical issues with remote data collection tools. To address these, it's important to establish clear protocols, provide thorough training to all study participants and collaborators, and utilize reliable remote monitoring technologies. Regular virtual check-ins and prompt technical support can also help mitigate issues quickly, fostering a productive and collaborative remote research environment.

What is the difference between Remote Observational Research vs Remote User Experience Research?

AspectRemote Observational ResearchRemote User Experience Research
Primary FocusObserving user behavior in natural settings without interferenceGathering user feedback and experiences to improve products
MethodsVideo recordings, ethnographic observation, contextual inquirySurveys, interviews, usability testing, remote sessions
Work EnvironmentField settings, participants' homes, online observation toolsRemote testing platforms, video calls, online surveys
Required SkillsObservation techniques, data analysis, ethnographyUser research, interview skills, data interpretation

Remote Observational Research and Remote User Experience Research both involve understanding user behavior remotely. Observational research emphasizes watching users in their natural environment, while UX research focuses on collecting user feedback to enhance digital products. Both roles often require similar skills and tools, but their core methods and objectives differ.

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Cities with the most Remote Observational Research job openings:

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The most popular types of Observational Research jobs are:

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Remote Observational Research jobs near you
Infographic showing various Remote Observational Research job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $46,222 per year, or $22.2 per hour.

Clinical Research Coordinator

Vitalief

Newark, NJ • Remote

$40 - $45/hr

Part-time

This job post has expired 3 days ago. Applications are no longer accepted.

Job description

ABOUT VITALIEF
Vitalief is a clinical research consulting firm focused exclusively on the clinical research industry, providing consulting, staffing, and technology-enabled services to academic medical centers, health systems, sponsors, CROs, and site networks. By combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients.
POSITION OVERVIEW
Vitalief is seeking an experienced Clinical Research Coordinator (CRC) to support a vascular/cardiovascular medical device clinical study for a leading New Jersey health system. This is an ideal opportunity for an experienced CRC seeking flexible, remote, part-time work with the potential for increased hours and eventual transition to a full-time, fully benefited Vitalief position as the study expands.
 
  • Meaningful Work: Support innovative cardiovascular medical device research with the potential to improve patient care.
  • Initial Workload: Approximately 2 to 4 patients enrolled per month, with 10 to 12 hours of work per enrolled patient (approximately 20 to 40 hours per month).
  • Flexible Schedule: Hours will vary based on patient enrollment and surgical procedures.
  • Remote Flexibility: Most study coordination activities can be performed remotely, including patient enrollment within 48 hours following surgery.
  • Growth Opportunity: The study is initially at one hospital and is expected to expand to three additional sites, increasing patient volume and CRC responsibilities.
  • Competitive Pay: $40 to $45/hour, based on experience.

RESPONSIBILITIES
  • Serve as the primary Clinical Research Coordinator for the study and work closely with the Principal Investigator and health system research team.
  • Identify, screen, and enroll eligible patients following their vascular heart medical device procedure.
  • Conduct remote patient enrollment within 48 hours following surgery, as permitted by the study protocol.
  • Conduct participant follow-up activities, including health status and other study-related calls.
  • Review patient medical records in EPIC to support eligibility determination and clinical data collection.
  • Complete electronic case report forms (eCRFs), perform accurate and timely data entry, and resolve data queries.
  • Maintain accurate source documentation and ensure study records are complete and up to date.
  • Maintain essential regulatory documentation, including investigator files, training records, licenses, and delegation logs.
  • Support IRB submissions, continuing reviews, amendments, and regulatory correspondence as needed.
  • Communicate with sponsors, CROs, investigators, IRBs, and internal research teams as needed.
  • Support monitoring activities, site meetings, issue resolution, and study closeout activities.
  • Help maintain study readiness and ensure timely completion of required study activities.
  • Manage work independently and adjust priorities based on patient enrollment, surgical schedules, and study requirements.
  • As additional hospital sites are added, support the expansion and coordination of study activities across multiple locations.

REQUIRED SKILLS
  • Bachelor's degree in health science, life science, nursing, clinical research, or a related field.
  • Minimum of 2 years of clinical research coordination experience supporting observational and/or interventional clinical trials.
  • Clinical research experience involving medical devices, cardiovascular/vascular studies, registries, or observational research preferred.
  • Experience with patient screening, informed consent, enrollment, and participant follow-up.
  • Experience using EPIC to review patient medical records, support patient eligibility, and facilitate clinical data collection.
  • Experience completing eCRFs, performing clinical data entry, and resolving data queries.
  • Experience maintaining regulatory documentation and supporting IRB submissions.
  • Knowledge of Good Clinical Practice (GCP) and clinical research regulations.
  • Proficiency with Microsoft Office and clinical research databases/CTMS systems.
  • Self-starter with the ability to work independently with limited day-to-day supervision.
  • Strong organizational and time-management skills.
  • Exceptional attention to detail and commitment to data quality and research compliance.
  • Strong written and verbal communication skills.
  • Ability to interact professionally with investigators, patients, sponsors, CROs, and health system personnel.
  • Flexibility to adjust work hours based on patient enrollment and surgical schedules.
  • Ability to work effectively in a remote environment.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing.
 

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