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Scientific Research Project Manager Jobs (NOW HIRING)

uthscsa.edu

Clinical Research Project Manager

San Antonio, TX · On-site

$65K - $83K/yr

Manages the oversight of clinical projects ensuring completion within specifications, established ... UT San Antonio serves approximately 42,000 students in 320 academic programs spanning science ...

Penn State University

$65K - $94K/yr

## Research Project Manager - Survey Research CenterApplyremote type: Hybridlocations: Penn State ... Providing cutting-edge recommendations and best practices for social science data collection.

Kaiser Permanente

$52K - $67K/yr

... for research projects; managing the execution of research studies including data gathering ... Bachelors degree in Public Health, Health Care Administration, Epidemiology, Health Sciences ...

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

As of Sep 11, 2026, the average yearly pay for scientific research project manager in the United States is $86,032.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,500.00 and $91,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Scientific Research Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $86,032 per year, or $41.4 per hour.

Clinical Research Project Manager

Valhalla, NY • On-site

New York Medical College
Colleges, Universities, and Professional Schools • 1 - 5K employees
Learn more about New York Medical Collegeexternal

$56K - $70K/yr

Full-time

Re-posted 9 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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