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Clinical Research Program Manager Jobs in Silver Spring, MD

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?

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?

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

With experts in biomedical science, software engineering, and program management, we focus on ... Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our ...

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

With experts in biomedical science, software engineering, and program management, we focus on ... Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Supports the creation and management of clinical websites and web-based tools. - Collaborate with ... Research Familiarity with STATA and NVivo Education and Certifications: Bachelor's Degree Required ...

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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 13, 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.
What are popular job titles related to Clinical Research Program Manager jobs in Silver Spring, MD? For Clinical Research Program Manager jobs in Silver Spring, MD, the most frequently searched job titles are:
What cities near Silver Spring, MD are hiring for Clinical Research Program Manager jobs? Cities near Silver Spring, MD with the most Clinical Research Program Manager job openings:
Clinical Research Nurse

Clinical Research Nurse

Pharmaron

Baltimore, MD

$48 - $62/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago


Job description

Position: Clinical Research Nurse

Schedule: 3-12 hour shifts per week, rotating schedule

Hourly Range: $48.00 - $62.00 / hr

Location: Baltimore, MD

Job Overview:

Pharmaron is seeking an experienced Clinical Research Nurse to join our dynamic clinical research team in Baltimore. This role is ideal for licensed nurses who want to gain or expand their experience in clinical research while contributing to studies that make a global impact. You will lead and support research activities, ensuring participant safety, protocol compliance, and high-quality data collection, all while working alongside a skilled and collaborative team.

Responsibilities:

  • Serve as the charge nurse during assigned shifts-coordinate staff assignments and provide clinical oversight
  • Guide participants through study protocols and explain procedures to ensure compliance and comfort
  • Manage the informed consent process from enrollment through study completion in accordance with ICH/FDA regulations
  • Perform protocol-specific procedures including investigational product administration, phlebotomy, IV placement, ECGs, vital signs, and specimen collection
  • Monitor participant safety, assess adverse events, and ensure accurate documentation
  • Maintain clinical protocol compliance and contribute to quality assurance efforts
  • Collaborate with physicians, clinical teams, and support staff to provide exceptional research subject care
  • Mentor and support Research Associates and Phlebotomists during clinical shifts
  • Uphold privacy standards, Good Clinical Practices (GCP), and company SOPs throughout all clinical operations

What We're Looking For:

  • Bachelors of Science in Nursing
  • General understanding of GCP/ICH Guidelines and Codes of Federal Regulations
  • Excellent time management skills and must be able to prioritize workload
  • Active Registered Nurse (RN) license in the State of Maryland
  • ACLS certification (or ability to obtain within 3 months of hire)
  • Experience with IVs, phlebotomy, and investigational product administration
  • Familiarity with Good Clinical Practice (GCP), ICH Guidelines, and FDA regulations
  • Strong time management, communication, and leadership skills
  • Comfortable working in a fast-paced, team-oriented environment
  • Ability to exert up to 50 lbs. occasionally and support physical clinical demands
  • Prior experience in a clinical research setting preferred

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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