ZipRecruiter

Log In

1

Oncology Research Project Manager Jobs in Ridgewood, NJ

next page

Showing results 1-20

All JobsOncology Research Project JobsOncology Research Project Manager JobsOncology Research Project Manager Jobs in Ridgewood, NJ

Oncology Research Project Manager information

See Ridgewood, NJ salary details

$50.6K

$87K

$133.6K

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

As of Aug 22, 2026, the average yearly pay for oncology research project manager in Ridgewood, NJ is $87,045.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,300.00 and $92,600.00 per year, depending on experience, location, and employer.

What does an oncology research project manager do?

An Oncology Research Project Manager oversees the planning, execution, and completion of research projects focused on cancer studies. They coordinate between multidisciplinary teams, ensure regulatory compliance, manage budgets and timelines, and facilitate communication among stakeholders. Their role is vital in advancing cancer research by ensuring projects run smoothly and meet scientific and ethical standards. They may also contribute to grant writing, data analysis, and reporting findings to sponsors or regulatory bodies.

What are the key skills and qualifications needed to thrive as an oncology research project manager?

To thrive as an Oncology Research Project Manager, you need expertise in clinical research processes, regulatory compliance, and project management, typically supported by a degree in a health-related field and experience in oncology studies. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as PMP or SOCRA/ACRP are highly valued. Exceptional organizational skills, attention to detail, and effective communication are crucial for coordinating teams and ensuring protocol adherence. These skills ensure research projects are executed efficiently, safely, and in compliance with regulatory standards, ultimately advancing oncology care.

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

Oncology Research Project Managers often navigate complex regulatory requirements, tight timelines, and coordination among multidisciplinary teams. Managing patient recruitment and retention in clinical trials can be particularly challenging due to strict eligibility criteria and the sensitive nature of oncology studies. Building strong communication channels, staying organized with detailed project plans, and fostering collaboration between clinical staff, sponsors, and regulatory bodies are key strategies for overcoming these challenges. Proactive risk assessment and adaptability are also essential for success in this role.

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

The top searched job categories for Oncology Research Project Manager jobs in Ridgewood, NJ are:

What cities near Ridgewood, NJ are hiring for Oncology Research Project Manager jobs?

Cities near Ridgewood, NJ with the most Oncology Research Project Manager job openings:

Oncology Research Project Manager jobs near you

Clinical Research Project Manager

New York Medical College

Valhalla, NY

$70K/yr

Full-time

Re-posted 18 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 otherinternal or commercial software tools and proven ability to learn and apply new software quicklyas projects require. Familiarity with REDCap preferred. Strong IT skills, including excellent knowledge of various software programs and packagesincluding 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 torequired 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 SalaryUSD $56,000.00/Yr.Maximum SalaryUSD $70,000.00/Yr.Employment Type: FULL_TIME

Apply