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Clinical Research Project Lead Jobs (NOW HIRING)

uthscsa.edu

Clinical Research Project Manager

San Antonio, TX · On-site

$65K - $83K/yr

... clinical projects ensuring completion within specifications, established operational objectives and assignments. Responsible for ensuring and maintaining the integrity and quality of the research ...

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Clinical Research Project Lead information

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How much do clinical research project lead jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for clinical research project lead in the United States is $63.00, according to ZipRecruiter salary data. Most workers in this role earn between $50.96 and $78.61 per hour, depending on experience, location, and employer.

What is a clinical research project lead?

A Clinical Research Project Lead is a professional responsible for overseeing and managing clinical research studies to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate study timelines, budgets, and resources, and act as a primary point of contact between research teams, sponsors, and regulatory bodies. Their duties also include monitoring study progress, resolving issues, and ensuring proper documentation and reporting. This role is critical for the successful execution of clinical trials and the advancement of medical knowledge.

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

To thrive as a Clinical Research Project Lead, you need expertise in clinical trial management, regulatory compliance, and a background in life sciences or a related field, often supported by a bachelor's or advanced degree. Familiarity with electronic data capture (EDC) systems, project management tools like MS Project, and certifications such as PMI or ACRP are highly valuable. Strong leadership, organizational skills, and effective communication help manage multidisciplinary teams and ensure project milestones are met. These competencies are essential for delivering high-quality research outcomes while maintaining regulatory standards and efficient project execution.

How does a clinical research project lead typically collaborate with cross-functional teams during a study?

A Clinical Research Project Lead works closely with a variety of cross-functional teams, including clinical operations, data management, regulatory affairs, and biostatistics. They coordinate meetings, facilitate communication, and ensure all teams are aligned with the study's timelines and goals. Effective collaboration is essential for resolving issues quickly, maintaining regulatory compliance, and keeping the study on schedule. Project Leads often act as the primary point of contact, fostering teamwork and ensuring that all stakeholders are updated on progress and changes.

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

AspectClinical Research Project LeadClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management experienceBachelor's degree in health sciences or related field, often with certification
Work EnvironmentLeads multiple projects, manages teams, oversees study progressSupports study activities, manages participant recruitment, data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic research centersHospitals, clinics, research institutions
Search & Comparison IntentUnderstanding leadership and project management roles in clinical researchFocus on study coordination and participant management

The Clinical Research Project Lead typically oversees multiple clinical studies, manages teams, and ensures project milestones are met. In contrast, the Clinical Research Coordinator handles day-to-day study activities, participant interactions, and data collection. Both roles are essential but differ in scope, responsibilities, and level of leadership within the clinical research process.

What cities are hiring for Clinical Research Project Lead jobs?

Cities with the most Clinical Research Project Lead job openings:

What states have the most Clinical Research Project Lead jobs?

States with the most job openings for Clinical Research Project Lead jobs include:

What are popular job titles related to Clinical Research Project Lead jobs?

For Clinical Research Project Lead jobs, the most frequently searched job titles are:

Infographic showing various Clinical Research Project Lead job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 87% Full Time, 6% Part Time, 5% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $131,045 per year, or $63 per hour.

Clinical Research Project Manager

Valhalla, NY • On-site

Touro University
See more jobs at Touro Universityexternal

$56K - $70K/yr

Full-time

Re-posted 6 days ago

Touro University rating

5.9

Company rating: 5.9 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

Job description

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.


  • 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

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.


USD $56,000.00/Yr.
USD $70,000.00/Yr.

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