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Remote Clinical Research Jobs in Raritan, NJ (NOW HIRING)

Overview The Virtual Clinical Coordinator (temp/fixed term) plays a critical role in supporting the execution of clinical research studies by coordinating and performing remote clinical activities in ...

This is a full-time position that is fully remote. What you'll do * Publish novel, high impact ... Experience supporting clinical research studies or research programs, including coordinating ...

Senior Clinical Research Associate - Oncology - New York ICON is a global healthcare intelligence ... Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ...

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Remote Clinical Research information

See Raritan, NJ salary details

$50.2K

$109.9K

$193.5K

How much do remote clinical research jobs pay per year?

As of Sep 6, 2026, the average yearly pay for remote clinical research in Raritan, NJ is $109,916.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,900.00 and $125,400.00 per year, depending on experience, location, and employer.

What is remote clinical research?

A Remote Clinical Research job involves conducting and managing clinical trials and research studies from a remote location, rather than in a traditional on-site setting. Responsibilities may include data collection, regulatory compliance, patient monitoring, and communication with study teams. These roles often use digital tools and electronic data capture systems to ensure research integrity and efficiency. Remote clinical research professionals typically work for pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This job offers flexibility while still contributing to medical advancements and patient care.

What are the key skills and qualifications needed to thrive in remote clinical research?

To thrive in Remote Clinical Research, a strong background in life sciences, research methodologies, and clinical trial protocols is essential, often supported by a relevant bachelor’s or master’s degree. Familiarity with tools such as Electronic Data Capture (EDC) systems, CTMS (Clinical Trial Management Systems), and certifications like Good Clinical Practice (GCP) are highly valued. Exceptional written and verbal communication, self-motivation, and organizational skills help remote researchers successfully collaborate and manage studies from a distance. These skills ensure rigorous data integrity, compliance with regulations, and effective teamwork in a remote setting.

What are some unique challenges and benefits of working in remote clinical research?

Working remotely in clinical research often requires you to be highly independent, organized, and proficient with digital collaboration tools, as you'll be coordinating with cross-functional teams and managing regulatory documentation from a distance. One challenge can be maintaining consistent communication with clinical sites and colleagues across different time zones, but many companies provide robust digital platforms to facilitate this. On the plus side, remote roles offer flexibility and a better work-life balance while still allowing you to contribute to impactful research. Many remote clinical research professionals report developing strong self-discipline and process management skills, which can open doors to advanced positions such as Clinical Research Associate or Project Manager.

What are the most commonly searched types of Clinical Research jobs in Raritan, NJ?

The most popular types of Clinical Research jobs in Raritan, NJ are:

What are popular job titles related to Remote Clinical Research jobs in Raritan, NJ?

For Remote Clinical Research jobs in Raritan, NJ, the most frequently searched job titles are:

What cities near Raritan, NJ are hiring for Remote Clinical Research jobs?

Cities near Raritan, NJ with the most Remote Clinical Research job openings:

Infographic showing various Remote Clinical Research job openings in Raritan, NJ as of August 2026, with employment types broken down into 3% As Needed, 68% Full Time, 21% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $109,916 per year, or $52.8 per hour.

Clinical Research Recruiter

Prism Vision Group

New Providence, NJ • On-site, Remote

$75/hr

Full-time

Posted yesterday

New


PRISM Vision Group rating

7.2

Company rating: 7.2 out of 10

Based on 15 frontline employees who took The Breakroom Quiz


Job description

This exempt role can be remote or based out of a Prism Vision Group location.

Compensation Range: $75.000.00 - $85,000.00 (Dependent on Experience)

The Clinical Research Recruiter I (CRR) is responsible for supporting centralized patient recruitment and pre-screening activities across Prism Vision Group's network of ophthalmology research sites. The CRR partners with research coordinators, physicians, office staff, and sponsors to identify potential clinical trial participants, conduct preliminary qualification reviews, and facilitate timely referral of eligible patients to site research teams. The role plays a critical part in achieving enrollment goals through proactive outreach, accurate documentation, and consistent follow-up with prospective participants.

Key Responsibilities 

  • Conduct centralized patient recruitment and pre-screening activities for clinical research studies across Prism Vision Group. 
  • Review referral opportunities, patient records, scheduling reports, and other recruitment sources to identify potential research candidates. 
  • Perform protocol-specific pre-screening to assess patient eligibility based on inclusion and exclusion criteria. 
  • Contact prospective participants via phone, text, email, and other approved communication methods to discuss research opportunities. 
  • Ensure timely follow-up on all referral opportunities and patient inquiries. 
  • Maintain accurate and complete documentation of recruitment activities within approved systems and databases. 
  • Track recruitment metrics, screening outcomes, enrollment conversions, and site performance indicators. 
  • Generate recruitment reports and provide updates to leadership, site teams, sponsors, and other stakeholders as needed. 
  • Collaborate with research coordinators, investigators, physicians, and office staff to support enrollment strategies and patient engagement initiatives. 
  • Participate in study kickoff meetings and develop recruitment summaries outlining eligibility criteria, target patient populations, outreach strategies, and enrollment goals. 
  • Escalate recruitment barriers, enrollment concerns, and operational issues to leadership as appropriate. 
  • Support implementation of new recruitment initiatives, technologies, workflows, and process improvement efforts. 
  • Participate in department, site, cross-functional, and sponsor meetings as required. 
  • Other duties as assigned. 

Knowledge 

  • Knowledge of clinical research processes, GCP guidelines, FDA regulations, and medical terminology. 
  • Understanding of patient recruitment, patient retention, and enrollment strategies within clinical research. 
  • Knowledge of ophthalmology clinical research preferred. 
  • Working knowledge of electronic medical records and patient database systems. 
  • Experience reviewing patient charts to identify potential clinical trial candidates. 

Skills 

  • Strong patient communication and customer service skills. 
  • Ability to build rapport with prospective study participants. 
  • Excellent verbal and written communication skills. 
  • Strong organizational, multitasking, and time management skills. 
  • Detail-oriented with excellent documentation practices. 
  • Proficiency in Microsoft Excel, Word, Outlook, PowerPoint, and CRM/recruitment tracking systems. 
  • Ability to achieve recruitment KPIs, enrollment goals, and conversion targets. 

Experience 

Minimum 

  • 2-3 years of experience in patient recruitment, clinical research recruitment, healthcare outreach, clinical research coordination, or a related healthcare role. 
Qualifications:

Knowledge 

  • Knowledge of clinical research processes, GCP guidelines, FDA regulations, and medical terminology. 
  • Understanding of patient recruitment, patient retention, and enrollment strategies within clinical research. 
  • Knowledge of ophthalmology clinical research preferred. 
  • Working knowledge of electronic medical records and patient database systems. 
  • Experience reviewing patient charts to identify potential clinical trial candidates. 

Skills 

  • Strong patient communication and customer service skills. 
  • Ability to build rapport with prospective study participants. 
  • Excellent verbal and written communication skills. 
  • Strong organizational, multitasking, and time management skills. 
  • Detail-oriented with excellent documentation practices. 
  • Proficiency in Microsoft Excel, Word, Outlook, PowerPoint, and CRM/recruitment tracking systems. 
  • Ability to achieve recruitment KPIs, enrollment goals, and conversion targets. 

Experience 

Minimum 

  • 2-3 years of experience in patient recruitment, clinical research recruitment, healthcare outreach, clinical research coordination, or a related healthcare role. 
Education:UNAVAILABLEEmployment Type: FULL_TIME

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