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Lead Clinical Research Associate Jobs (NOW HIRING)

The Program Lead will oversee all start-up operations across five clinical research centers, ensuring fast and efficient activation. The PL is responsible for the development, coordination, and ...

$100K/yr

... project lead(s). * Assists in preparing sites for audits and in resolving audit action items ... Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical ...

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... Lead site feasibility activities: distribute/collect questionnaires, evaluate responses, conduct ...

This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate ... May assist with or lead training of junior team members. * May assist or take lead in developing ...

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... Lead site feasibility activities: distribute/collect questionnaires, evaluate responses, conduct ...

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Lead Clinical Research Associate information

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$36K

$81.2K

$156K

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

As of Sep 13, 2026, the average yearly pay for lead clinical research associate in the United States is $81,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $90,000.00 per year, depending on experience, location, and employer.

What is a lead clinical research associate?

A Lead Clinical Research Associate (Lead CRA) is a senior-level professional responsible for overseeing and coordinating the activities of clinical research associates (CRAs) during clinical trials. They ensure that clinical studies are conducted in compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines. Lead CRAs often act as a liaison between the sponsor, study sites, and internal teams, providing training, guidance, and support to junior CRAs. They may also be involved in monitoring trial progress, resolving issues at study sites, and ensuring data quality and integrity throughout the clinical trial process.

How does a lead clinical research associate typically collaborate with study teams and site staff during a clinical trial?

A Lead Clinical Research Associate (Lead CRA) plays a pivotal role in coordinating communication between the sponsor, clinical trial sites, and internal study teams. They oversee and mentor CRAs, resolve site issues, and ensure compliance with protocols and regulations. Regularly, Lead CRAs participate in team meetings, provide guidance to site staff, and help troubleshoot operational challenges, ensuring smooth study progress and data integrity. This collaborative approach is essential for addressing site concerns swiftly and maintaining high-quality trial standards.

What are the key skills and qualifications needed to thrive as a lead clinical research associate, and why are they important?

To thrive as a Lead Clinical Research Associate, you need expertise in clinical trial management, regulatory compliance, and protocol development, typically supported by a life sciences degree and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is vital. Strong leadership, attention to detail, and effective communication set top performers apart in this role. These skills ensure that clinical trials are conducted efficiently, ethically, and in compliance with all regulatory standards.

What is the difference between Lead Clinical Research Associate vs Clinical Research Associate?

AspectLead Clinical Research AssociateClinical Research Associate
CredentialsBachelor's degree, often with experience; certifications like CCRP or RACBachelor's degree; certifications like CCRP or RAC
Work EnvironmentLeads study teams, manages site activities, oversees multiple sitesMonitors clinical sites, ensures protocol compliance, reports data
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentUnderstanding leadership roles in clinical trialsEntry to mid-level monitoring roles

The Lead Clinical Research Associate typically oversees multiple sites, manages study teams, and ensures protocol adherence, whereas the Clinical Research Associate focuses on monitoring individual sites and collecting data. Both roles require similar credentials and are used across the same industries, but the lead position involves more leadership responsibilities.

What cities are hiring for Lead Clinical Research Associate jobs?

Cities with the most Lead Clinical Research Associate job openings:

What are the most commonly searched types of Lead Clinical Research jobs?

The most popular types of Lead Clinical Research jobs are:

Who are the top companies hiring for Lead Clinical Research Associate jobs?

The top employers for Lead Clinical Research Associate jobs are:

What states have the most Lead Clinical Research Associate jobs?

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

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

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

Infographic showing various Lead Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $81,196 per year, or $39 per hour.

Program Lead, Clinical Research

New York, NY • On-site

NYULMC
Hospitals • 501 - 1,000 employees

Full-time

Medical, Retirement

Re-posted 20 days ago


NYU Langone Health rating

8.4

Company rating: 8.4 out of 10

Based on 250 frontline employees who took The Breakroom Quiz


Job description


NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.
For more information, go to med.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, Twitter and Instagram.
Position Summary:
We have an exciting opportunity to join our team as a Program Lead, Clinical Research.
In this role, the successful candidate The Clinical Translational Science Institute (CTSI), Clinical Research Centers (CRC) is seeking a highly motivated and organized individual to join our institution as a Program Lead (PL) reporting to the Executive Director of Clinical Research Operations. The Program Lead will oversee all start-up operations across five clinical research centers, ensuring fast and efficient activation. The PL is responsible for the development, coordination, and negotiation of clinical trial budgets, preparing cost assessments for industry and non-industry sponsored clinical trials, and ensuring that all budgeting activities comply with institutional policies, contractual obligations, and applicable regulations. The PL will work closely with principal investigators, departmental research teams, the Office of Science and Research (OSR) units of budgeting, contracts, sponsored programs, billing compliance, and the IRB and the CTSI clinical research center teams. The position also requires regular contact with sponsors, collaborating institutions, and federal agencies in negotiating budgets. The role requires expertise in project management, budgeting, and regulatory affairs.
Job Responsibilities:
  1. Study Start-Up and Clinical Trial Budgeting
    • Provides strategic and operational leadership for end-to-end study start-up and activation activities across the CTSI Clinical Research Centers portfolio, including protocol intake, feasibility review, operational assessments, budget development, regulatory coordination, and activation readiness.
    • Oversees the development and implementation of standardized center-wide start-up workflows, SOPs, operational dashboards, escalation pathways, and performance metrics to improve study activation timelines and operational efficiency.
    • Leads centralized clinical trial budgeting operations for industry-, foundation-, and federally sponsored research studies, including development of comprehensive internal budgets, prospective reimbursement analyses, coverage analyses, and research billing grids.
    • Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs, billing compliance, IRB, finance offices, and institutional service providers to ensure alignment across contractual, operational, financial, and regulatory timelines.
    • Oversees development and maintenance of institutional fee schedules and research service pricing methodologies to support sustainable clinical research operations.
    • Partners with executive leadership to identify operational risks, financial gaps, and process improvement opportunities related to study activation and clinical research center financial infrastructure.
    • Supports strategic initiatives focused on research growth, operational scalability, financial sustainability, and optimization of clinical trial activation performance throughout the clinical research centers to ensure appropriate pricing of clinical research procedures.

  1. Reporting, Communication, & Collaboration
  • Develops and delivers executive-level operational, financial, and performance reports for CTSI leadership, investigators, institutional stakeholders, and external sponsors.
  • Maintains strong collaborative relationships with investigators, research administrators, finance teams, compliance offices, and institutional leadership to facilitate efficient and compliant study activation.
  • Represents CTSI clinical research centers on institutional committees, operational workgroups, and strategic initiatives related to clinical research administration and research operations.
  • Participates in institutional planning activities focused on research process optimization, financial stewardship, and operational innovation.
  • Performs additional duties and strategic initiatives as assigned in support of CTSI and institutional research operations.

Minimum Qualifications:
To qualify you must have a Bachelor's degree in business administration, healthcare administration or related field. Minimum of 4 years of progressively responsible related experience coordinating clinical/research trials studies Proficiency in using various Microsoft Office applications such as Word, Excel, Access, Powerpoint and Outlook. Familiar with Internet applications. Effective oral and written communication skills, interpersonal skills, and organizational skills. Ability to interface effectively with all levels of management and must work and communicate effectively with both internal and external customers.
Preferred Qualifications:
o Master's degree or above in public health or research
o 5-10 years experience in clinical research administration and budgeting
o Direct experience in financial planning of clinical trials (strongly preferred)
o Ability to manage multiple projects simultaneously and deliver consistently high-quality outputs on time.
o Excellent organizational, project management, and time management skills. Attention to detail and commitment to maintaining high standards of quality.
o Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders.
o Ability to adapt to changing priorities and work in a fast-paced environment.
o Computer literacy required with proficiency of basic Microsoft Office software applications.
Qualified candidates must be able to effectively communicate with all levels of the organization.
NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents. At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package. Our offerings provide a robust support system for any stage of life, whether it's developing your career, starting a family, or saving for retirement. The support employees receive goes beyond a standard benefit offering, where employees have access to financial security benefits, a generous time-off program and employee resources groups for peer support. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Join us and experience the extensive resources and services designed to enhance your overall quality of life for you and your family.
NYU Grossman School of Medicine is an equal opportunity employer and committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. We require applications to be completed online.
View Know Your Rights: Workplace discrimination is illegal.
NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $84,577.93 - $101,223.89 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
To view the Pay Transparency Notice, please click here

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