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Clinical Research Program Manager Jobs in Silver Spring, MD

Pharmaron

Clinical Research Nurse

Baltimore, MD · On-site

$48 - $57/hr

Manage the informed consent process from enrollment through study completion in accordance with ICH ... Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity?

Pharmaron

Clinical Research Nurse

Baltimore, MD · On-site

$48 - $62/hr

Manage the informed consent process from enrollment through study completion in accordance with ICH ... Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity?

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Clinical Research Program Manager information

See Silver Spring, MD salary details

$46K

$95.7K

$154.6K

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

As of Jul 8, 2026, the average yearly pay for clinical research program manager in Silver Spring, MD is $95,731.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,900.00 and $108,500.00 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.
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RESEARCH PROG COORD-RIAO

RESEARCH PROG COORD-RIAO

LifeBridge Health

Baltimore, MD • On-site

Full-time

Re-posted 5 days ago

LifeBridge Health rating

6.2

Company rating: 6.2 out of 10

Based on 77 frontline employees who took The Breakroom Quiz

698th of 880 rated healthcare providers

Job description

Under limited supervision, the Research Program Coordinator role coordinates the RIAO Research Program, including clinical trial regulatory affairs and clinical trial and research data coordination.

Essential Functions include:

  • Prepares regulatory documents and monitors regulatory activities for assigned clinical trials.
  • Prepares protocol for initial and annual IRB (Institutional Review Board); submits protocol revisions and amendments for IRB review; submits Serious Adverse Events reports and Investigational Drug Safety Reports to the IRB; maintains IRB correspondence documentation for study sponsor and cooperative group audits.
  • Prepares regulatory documentation binders for study monitoring and audits by National Cooperative Groups (NCG)/Pharmaceutical companies/FDA; assists in preparation of patient charts for audits and monitoring visits.
  • Prepares initial Informed Patient Consent forms for study participation; prepares form revisions when requested by study sponsor and submits for IRB review.
  • Manages the day to day regulatory/protocol maintenance operations of the assigned clinical trials.
  • Assists with the implementation of the clinical research agreement, study budget and investigator contract, review and submission; responsible for annual protocol/research agreement renewal coordination.
  • Assists physicians with obtaining protocols of interest; prepares and submits site assessment documentation and regulatory package to study sponsors; coordinates and facilitates pre-study, study initiation and study monitoring visits.
  • Develops data collection system to provide necessary patient and physician communication, report generation and statistical output; manages and augments system as necessary; inputs information into the database and verifies accuracy.
  • Assists Clinical Research Nurses with patient data collection and submits research data to the NCG according to the protocol regulations; assures compliance with standards set by research groups for continued participation

QUALIFICATIONS/REQUIREMENTS

Basic professional knowledge; working knowledge of theory and practice within a specialized field

Education/Knowledge: Preferred- Bachelor's Degree

Health Science/Public Health or related field.

Experience: 1-3 years related exp

What LifeBridge Health employees say

Pay

Benefits

Hours and flexibility

Workplace

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About LifeBridge Health

Sourced by ZipRecruiter

LifeBridge Health is a $2B, 13,000 team member healthcare system that Cares Bravely for over 1 million patients annually throughout Maryland. We are comprised of 5 main healthcare centers: Sinai Hospital, Northwest Hospital, Carroll Hospital, Levindale Hebrew Geriatric Center and Hospital, and Grace Medical Center as well as several specialty and primary care locations throughout Baltimore.

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Baltimore, MD, US

Year founded

1988

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