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Freelance Clinical Research Associate Jobs in Ridgewood, NJ

Touro University

Clinical Research Associate

Hawthorne, NY · On-site

$48K - $60K/yr

Ensure compliance with the Good Clinical Practice guidelines in clinical research. * Monitor study patients for adverse events in collaboration with clinical team and report as required. * Enter data ...

Columbia University

Clinical Research Aide

Manhattan, NY · On-site

$90K/yr

The Assistant Clinical Research Manager is responsible for supporting the operational management of ... Show more Full-time Research Assistant/Associate (Survey Research Operations Manager).This position ...

IQVIA

Clinical Research Associate

Parsippany, NJ

$87K - $182K/yr

Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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All JobsClinical Research Associate JobsFreelance Clinical Research Associate JobsFreelance Clinical Research Associate Jobs in Ridgewood, NJ

Freelance Clinical Research Associate information

See Ridgewood, NJ salary details

$36.4K

$95.4K

$145.2K

How much do freelance clinical research associate jobs pay per year?

As of Aug 21, 2026, the average yearly pay for freelance clinical research associate in Ridgewood, NJ is $95,426.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $129,500.00 per year, depending on experience, location, and employer.

What is a freelance clinical research associate?

A Freelance Clinical Research Associate (CRA) is an independent professional who monitors clinical trials to ensure compliance with regulatory guidelines, protocols, and Good Clinical Practice (GCP). Unlike full-time CRAs, freelancers work on a contract basis for multiple sponsors, contract research organizations (CROs), or clinical sites. Their responsibilities include site visits, data verification, risk assessment, and communication with investigators. This role offers flexibility, diverse project opportunities, and control over workload but requires strong self-management and networking skills.

What are the key skills and qualifications needed to thrive as a freelance clinical research associate?

To thrive as a Freelance Clinical Research Associate, you need a strong background in clinical research, understanding of ICH-GCP guidelines, and typically a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as GCP training are commonly expected. Excellent organizational skills, self-motivation, and clear communication are essential soft skills for managing independent workloads and liaising with multiple stakeholders. These abilities ensure regulatory compliance, accurate data collection, and successful coordination of clinical trials across diverse settings.

What are the typical challenges faced by freelance clinical research associates, and how can they be managed?

As a freelance Clinical Research Associate, you'll often manage multiple studies or sites at once, requiring strong time management and organizational skills. Challenges can include juggling different sponsor requirements, keeping up with regulatory changes, and maintaining clear communication across virtual teams. Effective use of project management tools, regular updates with stakeholders, and continuous professional development help address these challenges. Freelancers often enjoy greater flexibility but must proactively seek new contracts and networking opportunities to maintain steady work. Being adaptable and detail-oriented are key traits to thrive in this dynamic environment.

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

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

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

The top searched job categories for Freelance Clinical Research Associate jobs in Ridgewood, NJ are:

What cities near Ridgewood, NJ are hiring for Freelance Clinical Research Associate jobs?

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Freelance Clinical Research Associate jobs near you

Senior Clinical Research Associate - Oncology

410 ICR United States USA

New York, NY

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago

Job description

Senior Clinical Research Associate - Oncology -

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.


What You Will Be Doing:

  • Serve as the primary point of contact between investigational sites and the sponsor

  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

  • Ensure site compliance with ICH-GCP, SOPs, and regulations

  • Maintain up-to-date documentation in CTMS and eTMF systems

  • Support and track site staff training and maintain compliance records

  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

  • Support subject recruitment and retention efforts at the site level

  • Oversee drug accountability and ensure proper storage, return, or destruction

  • Resolve data queries and drive timely, high-quality data entry

  • Document site progress and escalate risks or issues to the clinical team

  • Assist in tracking site budgets and ensuring timely site payments (as applicable)

  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

  • A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN

  • Eligible to work in United States without visa sponsorship

  • A clinical research professional with 3+ years of on-site monitoring experience in the pharmaceutical or CRO industry

  • Experienced across multiple therapeutic areas, ideally including Oncology (Prostate Cancer, and Lung Cancer) and Hematology

  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

  • A clear communicator, problem-solver, and collaborative team player

  • Willing and able to travel up to 50% for on-site monitoring visits across northeast region; preference given to candidates residing in NJ / NY near major HUB airports to support efficient regional travel


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