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

Senior Clinical Editor ICON plc is a world-leading healthcare intelligence and clinical research ... NR1 #LI- Remote What ICON can offer you: Our success depends on the quality of our people. That ...

Senior Patient Recruitment Lead - United States & Canada (Remote) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Director, Project Management - Remote, US (Boston, MA Preferred) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ...

Director, Business Development - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Clinical Project Manager (CNS/Rare Disease) - Remote, US ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving ...

Senior Director, Business Development - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Consulting Statistician

Philadelphia, PA · On-site +1

$110K - $184K/yr

... remote based, Canada or USA) Statistical Consulting Services * Communicates with clients and ... Reviews literature related to clinical research, assigned therapy areas and in the areas of clients ...

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Remote Clinical Research information

See Riverside, NJ salary details

$49.5K

$108.4K

$190.9K

How much do remote clinical research jobs pay per year?

As of Jun 23, 2026, the average yearly pay for remote clinical research in Riverside, NJ is $108,409.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,800.00 and $123,700.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Clinical Research position, and why are they important?

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 is a Remote Clinical Research job?

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 some unique challenges and benefits of working in a remote clinical research role?

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 Riverside, NJ? The most popular types of Clinical Research jobs in Riverside, NJ are:
What job categories do people searching Remote Clinical Research jobs in Riverside, NJ look for? The top searched job categories for Remote Clinical Research jobs in Riverside, NJ are:
What cities near Riverside, NJ are hiring for Remote Clinical Research jobs? Cities near Riverside, NJ with the most Remote Clinical Research job openings:
Senior Clinical Editor

Senior Clinical Editor

Icon plc

Blue Bell, PA • Remote

Full-time

Medical, Life, Retirement, PTO

Posted yesterday


Job description

Senior Clinical Editor

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

As a Senior Medical Editor at ICON, you will be responsible for ensuring the accuracy, clarity, and quality of scientific documents and publications related to clinical trials.

What You Will Do:

Your experience in editorial and content services will be key in delivering high-quality outcomes and mentoring colleagues.
Key responsibilities include:

  • Editing and proofreading a wide range of scientific documents, including clinical study reports, regulatory submissions, publications, and presentations, ensuring adherence to quality standards and consistency.

  • Collaborating with medical writers to improve the clarity and effectiveness of scientific content, providing guidance on structure, style, and language.

  • Ensuring compliance with applicable regulatory requirements, guidelines, and best practices in medical writing and publishing.

  • Providing mentorship and training to junior editors and medical writers, fostering a culture of continuous improvement and excellence in scientific communication.

  • Conducting thorough fact-checking and verification of data to ensure accuracy and reliability of published materials.

  • Staying updated with industry trends, regulatory changes, and advancements in medical writing and editing practices.

  • Participating in the development and implementation of standard operating procedures (SOPs) related to document editing and quality control.

Your Profile:

You will have a strong foundation in editorial and content services, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or communications-related field

  • Extensive experience in medical editing, with a strong understanding of clinical research and regulatory documentation. Experience with CSRs and submission documents editing.

  • Exceptional editing and proofreading skills, with a keen eye for detail and the ability to enhance the clarity and impact of scientific content.

  • Strong knowledge of medical terminology and scientific writing conventions, with experience in using editing style guides.

  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.

  • Proficiency in editing software and tools, as well as document management systems.

  • Demonstrated ability to manage multiple projects and meet deadlines in a fast-paced environment.

#LI-NR1

#LI- Remote

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family's needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply