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Remote Ppd Clinical Research Jobs in Ridgewood, NJ

ICON

Senior Clinical Research Associate

New York, NY · On-site +1

$110K - $138K/yr

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 ...

Nourish

Research Associate

New York, NY · On-site +1

This person will report into our Head of Research and work closely with our clinical operations, product, data, and commercial teams. This role is full-time and open to NYC-based or remote candidates.

Nourish

Research Associate

New York, NY · On-site +1

This person will report into our Head of Research and work closely with our clinical operations, product, data, and commercial teams. This role is full-time and open to NYC-based or remote candidates.

Nourish

Research Associate

New York, NY · On-site +1

This person will report into our Head of Research and work closely with our clinical operations, product, data, and commercial teams. This role is full-time and open to NYC-based or remote candidates.

Allen Spolden

Clinical Trial Associate

Manhattan, NY · Remote

$55K - $65K/yr

This is a remote position. This role offers the opportunity to support the planning and execution ... Clinical research experience preferred * Strong organizational and time management skills.

IQVIA

Contract Virtual Clinical Coordinator

New York, NY · Remote

$33K - $82K/yr

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 ...

IQVIA

Contract Virtual Clinical Coordinator

New York, NY · Remote

$33K - $82K/yr

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 ...

Garner Health

Clinical Researcher

New York, NY · On-site +1

$90K - $100K/yr

This role will report to the Director of Healthcare Research. You will be essential in helping ... This role is open to remote candidates across the U.S. For candidates based in New York City, the ...

IQVIA

Clinical Trial Psych Rater

New York, NY · Remote

$62K - $156K/yr

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

IQVIA

Clinical Trial Psych Rater

New Providence, NJ · Remote

$62K - $156K/yr

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

Mondo

Clinical Data Governance Lead

Manhattan, NY · Remote

$77 - $92/hr

Clinical Data Governance Lead, location is Remote. The start date is ASAP for this contract ... Partner with clinical researchers to understand data needs and identify existing datasets that ...

IQVIA

Clinical Project Lead, Oncology

Parsippany, NJ · Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... clinical research. Key Responsibilities Clinical Trial Delivery & Oversight * Lead end-to-end ...

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All JobsPpd Clinical Research JobsRemote Ppd Clinical Research JobsRemote Ppd Clinical Research Jobs in Ridgewood, NJ

Remote Ppd Clinical Research information

See Ridgewood, NJ salary details

$49.6K

$108.6K

$191.2K

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

As of Aug 18, 2026, the average yearly pay for remote ppd clinical research in Ridgewood, NJ is $108,601.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,000.00 and $123,900.00 per year, depending on experience, location, and employer.

What is a remote PPD Clinical Research professional?

A Remote PPD Clinical Research job involves working for PPD (Pharmaceutical Product Development), a global contract research organization, to support clinical trials and research projects from a remote location. Professionals in this role help design, manage, and monitor clinical studies to ensure compliance with protocols, regulatory standards, and data integrity. Responsibilities may include data management, coordinating with study sites, and supporting trial documentation. Working remotely allows employees to collaborate with international teams and clients while maintaining flexibility. This role is essential in advancing new treatments and therapies to market efficiently and safely.

How does working remotely as a PPD Clinical Research professional impact collaboration with on-site teams and study sites?

As a remote PPD Clinical Research professional, you will collaborate closely with on-site teams, investigators, and study coordinators through virtual communication platforms. While you may not be physically present, regular video calls, emails, and project management tools are used to maintain effective communication and ensure study protocols are followed. Adapting to different time zones and proactively addressing challenges in real-time are common aspects of the role. Strong organizational and interpersonal skills are essential for building trust and maintaining seamless coordination across dispersed teams.

What are the key skills and qualifications needed to thrive as a remote PPD Clinical Research professional?

To excel as a Remote PPD Clinical Research professional, you need a comprehensive understanding of clinical trial processes, regulatory guidelines (such as GCP), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and certifications like ACRP or SOCRA are typically valuable. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing studies and collaborating with distributed teams. These competencies ensure compliance, data integrity, and the successful execution of clinical research in a remote environment.

What job categories do people searching Remote Ppd Clinical Research jobs in Ridgewood, NJ look for?

The top searched job categories for Remote Ppd Clinical Research jobs in Ridgewood, NJ are:

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

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

Remote Ppd Clinical Research jobs near you
Infographic showing various Remote Ppd Clinical Research job openings in Ridgewood, NJ as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 100% Remote job distribution, with an average salary of $108,601 per year, or $52.2 per hour.

Senior Clinical Research Associate

ICON

New York, NY • On-site, Remote

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 4 hours ago

Job description

Senior Clinical Research Associate - Oncology - New York
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Responsibilities:
  • Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
  • Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites
  • Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials
  • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs
  • Promptly document monitoring activities and submit/approve visit reports
  • Manage site essential document collection and TMF reconciliation with site files
  • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals
  • Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution
  • Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
  • Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations
  • Support sites and the client's regulatory inspections
  • Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities
  • Lead site engagement initiatives and foster relationships with key Oncology sites and networks

Qualifications
  • Bachelor's degree (scientific field preferred)
  • 5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.
  • 1+ years early development trial experience
  • Solid tumor clinical trial experience is required
  • Experience utilizing Veeva systems is highly preferred
  • Demonstrated experience developing/maintaining site relationships and securing compliance
  • Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology
  • Experience collaborating with sites from initial engagement through close-out phases
  • Experience activating sites
  • Experience training site staff
  • Experience supporting sites and/or sponsors in regulatory inspections
  • Experience working within a Functional Services (or in-house) monitoring model is preferred
  • Willing to travel up to 50%

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
$110,520.00-$138,150.00
Are you a current ICON Employee? Please click here to apply

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