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Clinical Program Manager Jobs in New York (NOW HIRING)

IQVIA

Clinical Program Manager

Parsippany, NJ · On-site

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

IQVIA

Clinical Program Manager

Parsippany, NJ

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

Kite Pharma

Clinical Program Manager

Parsippany, NJ

Acts as team leader and builder; providing guidance and oversight for the successful management of all aspects of clinical trials within designated program budgets and timelines. * Leads cross ...

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All JobsClinical Program JobsClinical Program Manager JobsClinical Program Manager Jobs in New York

Clinical Program Manager information

See New York salary details

$48.7K

$101.3K

$163.6K

How much do clinical program manager jobs pay per year?

As of Jul 27, 2026, the average yearly pay for clinical 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.

How does a Clinical Program Manager typically collaborate with cross-functional teams to ensure successful clinical trial execution?

A Clinical Program Manager works closely with cross-functional teams, including clinical research associates, data managers, regulatory affairs, and medical monitors, to coordinate all aspects of clinical trials. They facilitate regular meetings, ensure clear communication, and resolve any issues that may affect timelines or data quality. This role is pivotal in aligning diverse team members toward shared goals, managing expectations, and adapting to evolving study requirements, which helps drive successful trial outcomes.

What is the difference between Clinical Program Manager vs Clinical Project Manager?

AspectClinical Program ManagerClinical Project Manager
CredentialsTypically requires a clinical background, such as RN, MSN, or related healthcare degree, along with project management certificationOften requires a project management certification (PMP) or equivalent; clinical background is preferred but not always mandatory
Work EnvironmentOversees multiple related projects within a clinical program, often in healthcare organizations or pharmaceutical companiesManages individual clinical trials or projects, usually within a larger program or portfolio
Employer & Industry UsageCommonly employed in healthcare, biotech, and pharmaceutical industries to coordinate broad clinical initiativesUsed across similar industries to manage specific clinical studies or trials

The Clinical Program Manager focuses on overseeing multiple related clinical projects and strategic initiatives, while the Clinical Project Manager manages individual clinical trials. Both roles require project management skills, but the Program Manager has a broader scope and strategic responsibilities.

What is a Clinical Program Manager?

A Clinical Program Manager is a professional responsible for overseeing the planning, coordination, and execution of clinical trials or healthcare programs within a medical or research organization. They ensure that clinical projects meet regulatory, ethical, and organizational standards, while managing timelines, budgets, and cross-functional teams. Clinical Program Managers also liaise with stakeholders, analyze data, and report on project progress to ensure successful outcomes. Their role is critical in advancing medical research and improving patient care.

What are the key skills and qualifications needed to thrive as a Clinical Program Manager, and why are they important?

To thrive as a Clinical Program Manager, you need a solid background in clinical research or healthcare management, often supported by a relevant degree and experience in program coordination. Familiarity with clinical trial management systems (CTMS), regulatory compliance protocols, and sometimes certifications like PMP or CCRA are commonly required. Strong leadership, organizational skills, and effective communication set top performers apart in this role. These skills are crucial for overseeing complex clinical programs, ensuring regulatory adherence, and leading multidisciplinary teams toward successful project outcomes.
What are the most commonly searched types of Clinical Program jobs in New York? The most popular types of Clinical Program jobs in New York are:
What are popular job titles related to Clinical Program Manager jobs in New York? For Clinical Program Manager jobs in New York, the most frequently searched job titles are:
What job categories do people searching Clinical Program Manager jobs in New York look for? The top searched job categories for Clinical Program Manager jobs in New York are:
What cities in New York are hiring for Clinical Program Manager jobs? Cities in New York with the most Clinical Program Manager job openings:
Clinical Program Manager jobs near you
Infographic showing various Clinical Program Manager job openings in New York as of July 2026, with employment types broken down into 85% Full Time, and 15% Temporary. Highlights an 100% In-person job distribution, with an average salary of $101,311 per year, or $48.7 per hour.
Clinical Program Manager

Clinical Program Manager

Pivotal Solutions

Manhattan, NY • On-site

Full-time

Posted 13 days ago

Job description


Position Overview:
The Clinical Program Manager (CPM) is responsible for the strategic planning, oversight, and execution of clinical programs. The CPM ensures that all clinical trials within the program are conducted in compliance with the highest ethical standards and in accordance with applicable regulatory requirements.
Key Responsibilities:
Strategic Planning and Oversight:
Lead the development and execution of comprehensive clinical development plans.
Collaborate with cross-functional teams to ensure alignment of clinical objectives with company goals.
Monitor and assess the competitive landscape and adjust clinical strategies as necessary.
Clinical Trial Management:
Oversee the design, planning, and implementation of clinical trials within the program.
Ensure that clinical trials are executed on time, within budget, and in compliance with Good Clinical Practice (GCP), regulatory requirements, and company SOPs.
Coordinate with clinical sites, CROs, and other vendors to ensure smooth trial execution.
Stakeholder Management:
Serve as the primary clinical contact for internal teams, investigators, consultants, and regulatory agencies.
Foster strong relationships with key opinion leaders in the therapeutic area.
Data Management and Reporting:
Oversee the collection, analysis, and interpretation of clinical data.
Ensure timely and accurate reporting of clinical trial results to regulatory agencies, as well as internal and external stakeholders.
Budget and Resource Management:
Develop and manage the clinical program budget.
Ensure efficient allocation and utilization of resources across the clinical program.
Risk Management:
Identify potential risks in clinical programs and develop mitigation strategies.
Ensure that all clinical activities adhere to safety and compliance standards.
Continuous Improvement:
Stay updated with the latest clinical research methodologies, regulatory requirements, and industry best practices.
Implement process improvements to enhance the efficiency and quality of clinical programs.
Requirements
Qualifications:
Bachelor's degree in a related field; advanced degree (e.g., MD, PhD, PharmD) preferred.
Minimum of 7 years of experience in clinical research, with at least 3 years in a program management or leadership role.
Strong knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
Proven track record of successfully managing complex clinical programs.
Excellent interpersonal, communication, and leadership skills.
Ability to work in a fast-paced environment and manage multiple priorities.
Proficiency in clinical trial management systems and related software.
Physical Requirements:
Ability to travel as needed for site visits, investigator meetings, and conferences.

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