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Clinical Research Program Manager Jobs (NOW HIRING)

Cook Children's

Research Program Manager

Fort Worth, TX · On-site

The Program Manager advances the organizational research priorities of Cook Children's Health Care System and supports the research enterprise of Cook Children's clinical and scientific centers. This ...

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Clinical Research Program Manager information

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$44.5K

$92.6K

$149.5K

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

As of Jun 20, 2026, the average yearly pay for clinical research program manager in the United States is $92,603.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $105,000.00 per year, depending on experience, location, and employer.

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

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.
More about Clinical Research Program Manager jobs
What cities are hiring for Clinical Research Program Manager jobs? Cities with the most Clinical Research Program Manager job openings:
What are the most commonly searched types of Clinical Research Program jobs? The most popular types of Clinical Research Program jobs are:
What states have the most Clinical Research Program Manager jobs? States with the most job openings for Clinical Research Program Manager jobs include:
What job categories do people searching Clinical Research Program Manager jobs look for? The top searched job categories for Clinical Research Program Manager jobs are:
Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 88% Full Time, 4% Part Time, 6% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $92,603 per year, or $44.5 per hour.
Senior Clinical Research Program Manager

Senior Clinical Research Program Manager

Northwell Health

Lake Success, NY • On-site

$75K - $126K/yr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Northwell Health rating

7.8

Company rating: 7.8 out of 10

Based on 550 frontline employees who took The Breakroom Quiz

134th of 873 rated healthcare providers

Job description

Job Description
Job Description
Provides management of research administration at a clinical site(s) including monitoring the quality and accuracy of clinical trial data. Follows the established monitoring Standard Operating Procedures (SOP) and protocol- specific monitoring plan. Participates in site initiations and trainings.
Job Responsibility
1.Trains, coaches, supports and mentors Site Clinical Research Managers and other team members.
2.Manages the clinical research sites including, but not limited to acting as primary contact for clinical research sites for questions related to the protocol conduct protocol, regulatory document completion, study supplies, client scheduling, and electronic data capture.
3.Provides on-site or remote monitoring of clinical research site activities to ensure compliance with protocols, SOPs and relevant federal and state regulatory and institutional policies.
4.Provides consultation during study start-up activities regarding development of study protocol, SOP or Case Report Forms (CRFs), site qualification, data collection and study conduct.
5.Patricipates in site initiations and trainings.
6.Assesses accuracy, completeness and timeliness of study records by performing source data verification, regulatory document and consent form review, adverse event reporting compliance review, and investigational product accountability.
7.Performs study close-out monitoring activities.
8.Provides pre-review assistance prior to regulatory inspections and submissions.
9.Provides guidance on regulatory submissions to the FDA which may include an Investigational New Drug (IND), Investigational Device Exemption (IDE), New Drug Application (NDA) or other research under the purview of the FDA.
10.Prepares and forwarding monitoring reports to program manager. Working with study staff to address any concerns.
11.Promotes overall compliance and quality with research conduct through participation in education and training activities for professional staff.
12.Assists in developing appropriate education and training sessions for investigators and clinicians involved in research.
13.Works on assignments that involve moderately complex to complex issues where the analysis of situations or data requires in-depth evaluation of variable factors.
14.Regularly makes new recommendations on new processes, tools, and services that can impact multiple projects and other functions.
15.May provide technical guidance and direction to support team members, contractors and/or other vendors.
16.May serve as project/technical lead for ongoing processes or short-term projects within function or family.
17.Performs related duties, as required.
Job Qualification
Bachelor's Degree or equivalent combination of education/related experience, required.
3-5 years relevant experience, required.
  • Working knowledge of FDA regulatory processes, including IND submissions, preferred
  • Familiarity with ClinicalTrials.gov registration and maintenance, preferred
  • Ability to manage multiple projects and collaborate across team, preferred
  • Experience in an academic medical center or cancer research environment, preferred
  • Exposure to IIT lifecycle from concept through activation, preferred
    Additional responsibilities for this position may include:
  • The Cancer Center is seeking an experienced Clinical Research Project Manager/ Site Activation Specialist to oversee investigator-initiated clinical studies (IIS) conducted in collaboration with industry sponsors and external participating sites. This role will serve as a central operational lead responsible for study management, sponsor coordination, regulatory submissions, external site activation, and ongoing oversight of multicenter oncology trials.
    • The ideal candidate will have experience in oncology clinical research, FDA and regulatory submissions, site activation/start-up activities. This individual will work closely with principal investigators, sponsors, CROs (clinical research organizations), regulatory teams, and collaborating institutions to ensure studies are conducted in compliance with federal regulations, institutional policies, and protocol requirements.

  • *Additional Salary Detail
    The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future.When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).

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