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Clinical Research Program Manager Jobs in New York

Research Program Manager - Oncology

Somerset, NJ ยท On-site

$115K - $145K/yr

  • Medical

  • Life

  • Retirement

  • PTO

POSITION SUMMARY Vitalief is seeking an experienced Clinical Research Program Manager to join our team as a full-time employee supporting interventional oncology clinical trials at a premier research ...

Research Program Manager - Oncology

Somerset, NJ ยท On-site

$115K - $145K/yr

  • Medical

  • Life

  • Retirement

  • PTO

POSITION SUMMARY Vitalief is seeking an experienced Clinical Research Program Manager to join our team as a full-time employee supporting interventional oncology clinical trials at a premier research ...

Research Program Manager

New York, NY ยท On-site

  • Medical

  • Retirement

The Program Manager-Research is responsible for overall lab and research management and operations, working to ensure the timely development of activities and execution of deliverables within the ...

Research Program Manager

Manhattan, NY ยท On-site

  • Medical

  • Retirement

The Program Manager-Research is responsible for overall lab and research management and operations, working to ensure the timely development of activities and execution of deliverables within the ...

The Assistant Clinical Research Manager is responsible for supporting the operational management of ... Show more Full-time Program Manager, Clinical Services (SUD).Job Category: Skilled Requisition ...

Research Program Manager

New York, NY ยท On-site

  • Medical

  • Retirement

We have an exciting opportunity to join our team as a Research Program Manager. In this role, the ... Experience with coordination of clinical trials and pre- and post-award grants administration.

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Showing results 1-20

Clinical Research Program Manager information

See New York salary details

$48.7K

$101.3K

$163.6K

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

As of Aug 20, 2026, the average yearly pay for clinical research program manager in New York is $101,311.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,300.00 and $114,900.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

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

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

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

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Program jobs in New York?

The most popular types of Clinical Research Program jobs in New York are:

What cities in New York are hiring for Clinical Research Program Manager jobs?

Cities in New York with the most Clinical Research Program Manager job openings:

Infographic showing various Clinical Research Program Manager job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $101,311 per year, or $48.7 per hour.

Program Manager Clinical Research

Montefiore Orthopedics

Manhattan, NY โ€ข On-site

$84 - $105/hr

Other

Posted 2 days ago

New


Job description

## Program Manager Clinical ResearchApplylocations: 111 East 210th Streettime type: Full timeposted on: Posted Todayjob requisition id: JR230073**City/State:**Bronx, New York**Grant Funded:**Yes**Department:**Cancer Clinical Trials Office**Work Shift:**Day**Work Days:**MON-FRI**Scheduled Hours:**9 AM-5:30 PM**Scheduled Daily Hours:**7.5 HOURS**Pay Range:**$84,000.00-$105,000.00The **Clinical Research Program Manager,** under the supervision of the Director of Quality Assurance, will provide compliance and quality assurance reviews for the Montefiore Einstein Cancer Clinical Trials Office. The Clinical Research Program Manager- Monitor will be responsible for all ongoing monitoring activities -patient case reviews, pharmacy reviews, regulatory reviews for Montefiore Einstein Cancer Center Investigator Initiated Trials (trials where MECC clinicians are the Sponsor Investigators/IND Holder). The CRM will provide routine reviews and determine if there are compliance concerns that warrant a formal of the trials. The duties of this position must be executed in accordance with Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), the Montefiore Einstein Cancer Center Data and Safety Monitoring Plan (DSMP), and any other applicable regulatory requirements.**The Clinical Research Program Manager will:*** Work under the direction of the Director, Quality Assurance and will provide constant feedback on findings and evaluation of instituted Corrective and Preventative Action Plans (CAPA).* Serve as the Administrator for the MECC Data and Safety Monitoring Committee.* Work with the Director, Quality Assurance to develop and support an eligibility review process for all patients enrolled on cancer clinical studies.**Requirements*** Bachelor's degree required, master's degree preferred* 5 years of work experience required* Minimum of 3 years of experience in clinical research* CCRP/CCRC Certification preferred* Prior experience with internal audits and/or FDA inspection preparations.* Demonstrated knowledge proficiency of and adherence to federal (FDA, OHRP, GCP, etc.), state, and other regulatory standards, requirements, and guidelines related to clinical research* Strong working knowledge of ongoing monitoring techniques (including criteria development and trending)* Strong working knowledge of quality management principles, tools, and risk management techniques* Analytical and critical thinking skills to recognize trends* Demonstrated ability to manage projects: ability to prioritize, identify barriers and meet deadlines* Ability to prioritize, organize, plan, and implement services as well as handle multiple projects/problems simultaneously* Demonstrated communication, leadership, and team building skills: evidence of this should include dealing well with people, effective problem solving, appropriately confronting issues, motivating others as individuals and as groups, planning, organizing and directing the activities of others* Demonstrated skill in working with minimal supervision* Effective written and verbal communication #J-18808-Ljbffr