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Clinical Program Manager Jobs in Frederick, MD (NOW HIRING)

Global Clinical Head Renal

Gaithersburg, MD ยท On-site

$331K - $497K/yr

... programs in a dynamic global setting. This role reports to the Vice President, Clinical CVR and is ... management plans. Experience with global regulatory submissions and interacting with major ...

Global Clinical Head Renal

Gaithersburg, MD ยท On-site

$331K - $497K/yr

Perform medical prioritization of clinical activities within the clinical program * Single-point ... Experience assessing the benefit/risk profile of an asset and creating patient risk management ...

... clinical-stage program teams in the development of the Immunocore portfolio by effectively ... management leadership by providing active input into the project strategy & vision, ensuring ...

Showing results 21-40

Clinical Program Manager information

See Frederick, MD salary details

$44.2K

$92.1K

$148.6K

How much do clinical program manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical program manager in Frederick, MD is $92,073.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $104,400.00 per year, depending on experience, location, and employer.

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?

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.

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.

How much do clinical program managers make?

Clinical Program Managers in California typically earn between $100,000 and $150,000 annually, depending on experience, certifications, and the size of the organization. Salaries can vary based on the complexity of clinical programs and the level of responsibility involved.

What degree do I need to be a clinical program manager?

A clinical program manager typically needs at least a bachelor's degree in a healthcare-related field such as nursing, public health, or healthcare administration. Many employers prefer candidates with a master's degree, such as an MBA or a master's in healthcare administration, along with relevant experience and strong project management skills. Certifications like PMP or RAC may also enhance qualifications for this role.

What does a clinical program manager do?

A clinical program manager oversees the planning, implementation, and management of clinical trials and research programs. They coordinate teams, ensure compliance with regulatory standards, and monitor project progress using tools like project management software. Strong organizational, communication, and regulatory knowledge are essential for success in this role.

What job categories do people searching Clinical Program Manager jobs in Frederick, MD look for?

The top searched job categories for Clinical Program Manager jobs in Frederick, MD are:

What cities near Frederick, MD are hiring for Clinical Program Manager jobs?

Cities near Frederick, MD with the most Clinical Program Manager job openings:

Infographic showing various Clinical Program Manager job openings in Frederick, MD as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $92,073 per year, or $44.3 per hour.

Head of Clinical Operations ( On site role)

Precigen, Inc

Germantown, MD โ€ข On-site

Full-time

Re-posted 20 days ago


Job description

Precigen is seeking a highly motivated and skilled Head of Clinical Operations (level determined by candidate experience), to drive our clinical trial programs to develop next generation gene and cell therapies focused in immuno-oncology, autoimmune disorders, and infectious diseases. Reporting to the Head of Clinical Operations, this role is responsible for driving organizational strategy and overall execution of clinical program(s) to align with corporate objectives, collaborating with executive leadership and external stakeholders to drive the success of our clinical programs.  The position will lead a high-performing Clinical Operation team to ensure work quality, timeliness and adherence to budget. 

The candidate will have a strong knowledge of global regulatory guidelines, strong organization and time management skills, and demonstrate focus to output/deliverables.

DUTIES AND RESPONSIBILITIES

  • Oversight of the execution of all clinical trials 
  • Ensures all trials are conducted in accordance with applicable SOPs, ICH, GCP and other applicable regulations.
  • Responsibility for meeting timelines and the execution of clinical studies making sure deliverables, milestones, and budget parameters are met. Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a global environment is required.
  • Manages resources and external vendors efficiently
  • Responsible for overall budget forecasting and management
  • Maintains and provides relevant and accurate information for monthly study reports (including enrollment curves, timelines, analysis of the study status and identification of potential risks) Clinical Trial material (CTM) Management, budget, and finances, change orders, contracts.
  • Provide Clinical Operations expertise in cross-functional meetings and works closely with cross functional members to ensure the quality and in accordance with Precigen SOPs and global regulatory guidelines

EDUCATION AND EXPERIENCE

  • PhD, MD or Bachelors in medical or life science, regulatory science, or related field.
  • Strong understanding of global regulatory guidelines and processes.
  • Minimum of ten (10)+ years progressive experience in pharma/biopharma clinical operations.
  • Experience with biologics/gene therapy is preferred.

 

DESIRED KEY COMPETENCIES

  • Ability to understand and execute on the company’s mission and values.
  • Exceptional organization skills with strong attention to detail.
  • Strong personal leadership and self-direction.
  • Clear communication in both oral and written form.
  • Demonstrated ability to work with and coordinate demands from multiple stakeholders.
  • Exhibition of the highest degree of ethical standards and trustworthiness.
  • Advanced skills in Microsoft Word, Adobe Acrobat Professional®, and clinical trial management systems (CTMS).