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Clinical Informatics Jobs in Frederick, MD (NOW HIRING)

Bachelor's degree in Computer Science, Information Systems, Health Informatics, Clinical Research, or related field. * Minimum 5 years of clinical database development experience. * Experience with ...

Bachelor's degree in Computer Science, Information Systems, Health Informatics, Clinical Research, or related field. * Minimum 5 years of clinical database development experience. * Experience with ...

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Clinical Informatics information

See Frederick, MD salary details

$51.7K

$103K

$163.1K

How much do clinical informatics jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical informatics in Frederick, MD is $103,003.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,600.00 and $114,800.00 per year, depending on experience, location, and employer.

What is clinical informatics?

Clinical informatics is a field within the discipline of information technology. The purpose of clinical informatics is to implement technology and theories in order to collect, store, and modify clinical information and electronic records to improve patient care and information sharing among healthcare professionals. Clinical informatics investigates the most efficient and user-friendly ways data can be organized, structured, shared, and accessed. It has practical implications for healthcare provision throughout the industry, including at hospitals, clinics, and military and research facilities.

What is clinical informatics?

Clinical informatics is a field that focuses on the use of information technology and data to improve patient care and healthcare outcomes. Professionals in this area work at the intersection of healthcare, computer science, and information management to design, implement, and optimize electronic health records, clinical decision support systems, and other digital tools. Their goal is to streamline healthcare processes, enhance patient safety, and ensure that clinicians have access to accurate and timely information. Clinical informaticists often collaborate with physicians, nurses, IT professionals, and administrators to bridge the gap between clinical practice and technology.

What are the key skills and qualifications needed to thrive as a clinical informatics specialist, and why are they important?

To thrive as a Clinical Informatics specialist, you need a solid background in healthcare, information technology, and data analysis, often supported by a degree in health informatics or a related field. Familiarity with electronic health record (EHR) systems, clinical decision support tools, and certifications such as Certified Professional in Healthcare Information and Management Systems (CPHIMS) are commonly required. Strong problem-solving abilities, effective communication, and the capacity to bridge clinical and technical teams are standout soft skills. These competencies are essential for optimizing healthcare delivery, ensuring data accuracy, and facilitating the adoption of technology in clinical environments.

How does a clinical informatics professional typically collaborate with healthcare providers and IT teams?

Clinical Informatics professionals play a key bridging role between healthcare providers and IT departments. They work closely with clinicians to understand workflow needs and translate those requirements into technical solutions, such as optimizing electronic health records (EHR) or implementing new clinical decision support tools. Regular collaboration involves facilitating training sessions, gathering feedback, and troubleshooting system issues to ensure that technology effectively supports patient care. This cross-functional teamwork is essential for successful adoption and ongoing improvement of health information systems.

What is the difference between Clinical Informatics vs Medical Informatics?

AspectClinical InformaticsMedical Informatics
CredentialsOften requires certifications like CAHIMS or CPHIMSSimilar certifications, with additional focus on broader healthcare data
Work EnvironmentHospitals, clinics, healthcare systemsResearch institutions, healthcare IT companies, academia
Employer & IndustryHealthcare providers, hospitalsHealthcare technology firms, research organizations
Search & Comparison IntentFocuses on clinical settings and patient careEncompasses broader healthcare data management and policy

Clinical Informatics primarily concentrates on applying informatics to improve patient care within clinical settings. Medical Informatics has a broader scope, including healthcare data management, research, and policy. Both roles require similar certifications and often overlap in skills, but their focus areas differ based on work environment and industry applications.

What do you do in clinical informatics?

A clinical informatics professional designs, implements, and manages health information systems to improve patient care and healthcare operations. They analyze data, optimize electronic health records (EHR) systems, and collaborate with healthcare providers to ensure technology supports clinical workflows effectively.

What is the best degree for clinical informatics?

A master's degree in health informatics, healthcare administration, or a related field is typically preferred for clinical informatics roles. Relevant skills include knowledge of healthcare systems, data management, and proficiency with electronic health records (EHR) systems, often supported by certifications like Certified Health Data Analyst (CHDA) or Certified Professional in Healthcare Information and Management Systems (CPHIMS).

What are popular job titles related to Clinical Informatics jobs in Frederick, MD?

For Clinical Informatics jobs in Frederick, MD, the most frequently searched job titles are:

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

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

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

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

Infographic showing various Clinical Informatics job openings in Frederick, MD as of August 2026, with employment types broken down into 100% Full Time. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $103,003 per year, or $49.5 per hour.

Project Toxicologist, Director - Oncology Targeted Delivery (OTD) Safety Science, Clinical Pharma...

AstraZeneca

Gaithersburg, MD • On-site

$184K - $276K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago


Key responsibilities

  • Design and oversee regulatory and investigative toxicology programs to predict, assess, and mitigate target- and modality-related safety risks.

  • Apply toxicology expertise to support development decisions by anticipating clinical safety risks and providing data-driven recommendations.

  • Integrate in vitro, in silico, and in vivo approaches with emerging technologies to address complex safety questions.


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical


Job description

At AstraZeneca, our ambition is to eliminate cancer as a cause of death. Our pioneering oncology pipeline reflects this mission, and our Oncology Targeted Delivery (OTD) Safety team plays a critical role in advancing transformative therapies to patients. We are seeking a passionate and highly motivated Director, Project Toxicologist to join our OTD Safety group.

This role will focus on novel targeted oncology therapies, including radioconjugates, antibody-drug conjugates (ADCs), and small molecules. Experience with radioconjugates is particularly valued; however, candidates with expertise in other relevant modalities are encouraged to apply. As a Project Toxicologist, you will partner with cross-functional teams across Oncology R&D, bridging discovery and regulatory toxicology.

You will develop innovative safety strategies, guide candidate selection, inform regulatory approaches, and help shape the future of oncology safety science. LOCATIONS: Cambridge, MA (Kendall Square) or Gaithersburg, MD What you'll do Lead toxicology strategies: Design and oversee regulatory and investigative toxicology programs to predict, assess, and mitigate target- and modality-related safety risks. Support development decisions: Apply your toxicology expertise to anticipate clinical safety risks and provide data-driven recommendations across discovery and development programs.

Advance safety science: Integrate in vitro, in silico, and in vivo approaches with emerging technologies, including organ-on-chip, imaging, and omics, to address complex safety questions. Communicate integrated risk assessments: Present scientific conclusions and safety strategies to governance bodies and contribute to regulatory submissions. Provide regulatory and scientific leadership: Maintain and expand expertise in regulatory standards, preclinical safety, and modality-specific toxicology while anticipating industry trends and evolving methodologies.

Support external opportunities: Provide strategic toxicology input for in-licensing evaluations, due diligence activities, and external collaborations. Build scientific influence: Advance Oncology Safety science through internal and external collaborations, publications, conference participation, and thought leadership. Develop people and partnerships: Contribute to an inclusive, collaborative environment and support the development of colleagues across teams and geographies.

Essential qualifications and experience Education: PhD, DABT, or an advanced university degree in toxicology, pharmacology, oncology, or a related scientific discipline, together with a strong scientific track record. Professional experience: Typically, at least 10 years of experience in project toxicology, investigative toxicology, regulatory toxicology, or related safety-focused roles within the pharmaceutical, biotechnology, or CRO sector. Alternative experience pathway: Candidates with a minimum bachelor's degree and substantial additional pharmaceutical industry experience may also be considered, including candidates with approximately 15 or more years of relevant experience.

Oncology expertise: Deep understanding of oncology drug discovery and development, with a demonstrated ability to deliver toxicology programs supporting IND filings and broader development milestones. Modality expertise: Experience with radioconjugates or ADCs is preferred. Familiarity with small-molecule oncology therapeutics is also valuable.

Translational safety skills: Experience applying in vitro, in silico, and in vivo tools to predict and characterize potential clinical safety risks. Leadership and collaboration: Ability to coordinate multiple projects across functions and geographies while working effectively in a complex, matrixed environment. Communication and influence: Strong scientific communication, interpersonal, and influencing skills, with the ability to inform decisions among scientific, clinical, and regulatory stakeholders.

Commitment to inclusion: Demonstrated commitment to inclusion, diversity, collaboration, and team development, consistent with AstraZeneca's Great Place to Work objectives. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions.

That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.

Join us in our unique and ambitious world. The annual base salary for this position ranges from $184,538 and $276,808 USD Annual. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.

If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. AstraZeneca is where science meets innovation to create impactful solutions. We challenge the status quo by leveraging data to drive scientific breakthroughs that make a tangible difference in patients' lives.

Our collaborative environment fosters learning and growth, empowering you to contribute to meaningful research across global Therapy Areas. With countless opportunities for development, AstraZeneca is committed to investing in technology and expanding knowledge to maximize impact. Ready to make a difference.

Apply now to join our team and be part of something extraordinary. Date Posted 21-Aug-2026 Closing Date Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics.

If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB