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Clinical Research Project Manager Jobs in Paramus, NJ

Winaxis

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

Key Responsibilities Coordinate and manage clinical research studies in compliance with study ... projects How to Apply Interested candidates can submit their updated resume along with a cover ...

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Clinical Research Project Manager information

See Paramus, NJ salary details

$50.6K

$87.1K

$133.6K

How much do clinical research project manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for clinical research project manager in Paramus, NJ is $87,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $92,600.00 per year, depending on experience, location, and employer.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are the key skills and qualifications needed to thrive as a clinical research project manager?

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are some common challenges faced by clinical research project managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What are popular job titles related to Clinical Research Project Manager jobs in Paramus, NJ?

For Clinical Research Project Manager jobs in Paramus, NJ, the most frequently searched job titles are:

What job categories do people searching Clinical Research Project Manager jobs in Paramus, NJ look for?

The top searched job categories for Clinical Research Project Manager jobs in Paramus, NJ are:

What cities near Paramus, NJ are hiring for Clinical Research Project Manager jobs?

Cities near Paramus, NJ with the most Clinical Research Project Manager job openings:

Clinical Research Project Manager jobs near you
Infographic showing various Clinical Research Project Manager job openings in Paramus, NJ as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $87,057 per year, or $41.9 per hour.

Clinical Research Project Manager

New York Medical College

Valhalla, NY • On-site

$56K - $70K/yr

Full-time

Re-posted 2 days ago

Job description

Overview
The candidate will report to the Vice President of Research. Incumbent will manage all aspects of ongoingresearch studies. Attention to detail, self-starter, well organized as well as good communication skills. Applicant must adhere to Patient confidentially. The individual will be responsible for the oversight of studies conducted out of the clinical trials unit, and as such, will be responsible for contracts, oversee the research coordinators and study progress reports, orders, and other tasks as needed.
Responsibilities
  • Monitor study metrics and site performance using standard study management tools.
  • Oversee the individual study progress over duration of each project.
  • Direct liaison between sponsors/investigators and the research coordinator or Vice President
  • Establish research data and work flow plans.
  • Contribute to the development and implementation of SOPs, project-specific procedures, and technical guidance documents, patient acquisition plans, etc.
  • Direct establishment of clinical and analytical study related protocols and documents, as well as research/clinical data analysis.
  • Manage the orders, sample deliveries and supplies required for each study.
  • Interface with investigational sites, clinical consultants, and labs.
  • Management of research data sites and renewal terms related with each study and CTU functions.
  • Direct all aspects of research data generation and analysis including external site clinical studies and internal analytical studies.
  • Drive internal communication, including timelines, budget, progress, and project needs for clinical trials to product teams and senior management.
  • Interface with ORA, IRB, WMC and other pharmaceutical/hospital research offices

Qualifications
Education requirement: Bachelor's degree in biology, mathematics, computer science, natural sciences or related areas.
Licenses or certifications: CITI
Technical/Computer skills:
• Ability to use a combination of validated Electronic Data Capture (EDC) systems and/or other
internal or commercial software tools and proven ability to learn and apply new software quickly
as projects require. Familiarity with REDCap preferred.
• Strong IT skills, including excellent knowledge of various software programs and packages
including MS Word, Excel, Access
Prior experience: Minimum of two years of related professional experience
Skills:
• Ability to multi-task and meet established deadlines.
• Ability to work effectively both as part of a project team and independently is essential
• Excellent oral and written English communication skills.
• Proven experience using data management systems, tools and processes to support multi-site, multimode research studies.
• Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to
required guidelines, SOPs and client expectations.
• Good organizational and analytical/problem-solving skills with strong attention to detail.
• Ability to work productively with minimal supervision.
• Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs.
• Strong customer focus and excellent interpersonal skills.
To qualify, applicants must be legally authorized to work in the United States and should not require now, or in the future, sponsorship for employment visa status.
Minimum Salary
USD $56,000.00/Yr.
Maximum Salary
USD $70,000.00/Yr.

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