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Clinical Informatics Jobs in Laurel, MD (NOW HIRING)

Pharmaron

Clinical Informatics Specialist

Baltimore, MD · On-site

$24 - $30/hr

Position: Clinical Informatics Specialist Salary Range: $24.00/hr. - $30.00/hr. Location: Baltimore, MD (On-site) About Pharmaron Pharmaron is a global contract research and manufacturing ...

Trilogy Federal LLC

Clinical Informaticist

Arlington, VA · On-site

$100 - $118/hr

The Clinical Informaticist will apply clinical informatics expertise to assess and improve healthcare information systems, clinical workflows, and end-user processes. The Clinical Informaticist ...

Pharmaron

Clinical Informatics Specialist

Baltimore, MD · On-site

$24 - $30/hr

Clinical Informatics Specialist Salary Range: $24.00/hr. - $30.00/hr.Location: Baltimore, MD (On-site)About PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO ...

Trilogy Federal

Clinical Informaticist

Arlington, VA · Remote

$100K - $118K/yr

The Clinical Informaticist will apply clinical informatics expertise to assess and improve healthcare information systems, clinical workflows, and end-user processes. The Clinical Informaticist ...

Trilogy Federal

Clinical Informaticist

Arlington, VA · On-site

$100K - $118K/yr

The Clinical Informaticist will apply clinical informatics expertise to assess and improve healthcare information systems, clinical workflows, and end-user processes. The Clinical Informaticist ...

Trilogy Federal

Clinical Informaticist

Arlington, VA · On-site +1

$100K - $118K/yr

The Clinical Informaticist will apply clinical informatics expertise to assess and improve healthcare information systems, clinical workflows, and end-user processes. The Clinical Informaticist ...

Red Pulley, Inc.

Clinical Informaticist

Washington, DC · On-site +1

Bachelor's degree in Nursing, Health Informatics, Healthcare Administration, or a related clinical field * Minimum 3 years of demonstrated experience in clinical informatics, healthcare operations ...

Red Pulley, Inc

Clinical Informaticist

Washington, DC · On-site

Bachelor's degree in Nursing, Health Informatics, Healthcare Administration, or a related clinical field * Minimum 3 years of demonstrated experience in clinical informatics, healthcare operations ...

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Showing results 21-40

All JobsClinical Informatics JobsClinical Informatics Jobs in Laurel, MD

Clinical Informatics information

See Laurel, MD salary details

$51.6K

$102.7K

$162.6K

How much do clinical informatics jobs pay per year?

As of Sep 5, 2026, the average yearly pay for clinical informatics in Laurel, MD is $102,712.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,400.00 and $114,500.00 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).
More about Clinical Informatics jobs

What are the most commonly searched types of Clinical Informatics jobs in Laurel, MD?

The most popular types of Clinical Informatics jobs in Laurel, MD are:

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

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

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

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

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

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

Clinical Informatics jobs near you
Infographic showing various Clinical Informatics job openings in Laurel, MD as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 17% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $102,712 per year, or $49.4 per hour.

Clinical Informatics Specialist

Pharmaron

Baltimore, MD • On-site

$24 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

Position: Clinical Informatics Specialist
Salary Range: $24.00/hr. - $30.00/hr.
Location: Baltimore, MD (On-site)
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
Responsible for providing comprehensive protocol details and identifying key data collection points necessary for the Clinical Applications Team to successfully create and configure the study build within our ClinSpark database. This involves thoroughly understanding the study protocol, extracting relevant information, and translating it into actionable items for database setup. The role ensures that all critical data collection elements are accurately captured and properly integrated into the ClinSpark system, facilitating seamless data management and analysis throughout the study. Additionally, it includes ongoing collaboration with the Clinical Applications Team to address any protocol changes or updates, ensuring the database remains aligned with study requirements and compliance standards.
Key Responsibilities
  • Conducts clinical research in compliance with all applicable regulations, including but not limited to GCDMP, ICH GCP, and FDA 21 CFR Part 11 and company SOPs.
  • Demonstrates knowledge and application of all privacy and safety standards as they relate to job responsibilities, human research subjects, staff, and the general operation of the unit.
  • Interacts and communicates with, as well as delegates to (as necessary) all internal departments to achieve successful coordination during duration of study.
  • Performs a comprehensive evaluation of the initial and subsequent versions of the protocol and informed consent forms prior to IRB submission.
  • Maintains detailed knowledge and understanding of assigned protocols, including all protocol requirements for participant/subject visits, obtaining informed consent, visit schedules, tests, procedures, and laboratory information.
  • Provides comprehensive protocol details and identifies key data collection points in a source template for ClinSpark electronic case report forms (eCRF).
  • Performs a quality check review of all study data collection forms against the IRB approved protocol, protocol clarification letters, and other study specific documents and provides feedback.
  • Attends project Kick-off meetings and Site Initiation Visits and any meetings between Sponsor and Pharmaron regarding the ClinSpark build and/or updates for the duration of the study.
  • Confirms IRB approval has been obtained prior to study initiation and activation in ClinSpark.
  • Confirms Sponsor has given signed approval for Clinspark activation.
  • Maintains and shares Clinspark database plans and review logs.
  • Maintains all final plans, logs and eCRFs for TMF filing.
  • Confirms the details of study-specific laboratory specimen collection containers with the laboratory manager or designee.
  • Performs a quality control review of the study-specific activity worksheets against the IRB approved protocol and ClinSpark eCRFs.
  • Reviews EDC case report forms, when available, for each study against the IRB approved protocol and provide recommendations, as deemed necessary.
  • Ensures ClinSpark eCRFs align with any EDC case report forms, if applicable.
  • Reviews ClinSpark eCRFs and activity plans for each study against the IRB approved protocol and provide any recommendations, as necessary.
  • Completes all ClinSpark User Acceptance Testing (UAT) including but not limited to initial testing and any updates throughout the study.
  • Serves as the primary liaison for all other departments' proposed modifications to the eCRFs in ClinSpark.
  • Communicates actively with Laboratory, Pharmacy, Clinical Operations, Medical Staff, Project Management, Biostatistics and Data Management throughout the study build process.
  • Reviews clinical laboratory panels against the IRB approved protocol.
  • Attends meetings with the Clinical Applications Team to provide feedback about current processes.
  • Works in collaboration with the Project Manager to ensure database build timelines are met.

What We're Looking For
  • Bachelor of Science in related field + 1 year as a Clinical Research Coordinator (CRC) or 3 years of experience in a clinical research environment.

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 25,000 employees and operations in the US, UK, China, and Singapore. 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:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

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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