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Remote Clinical Informatics Jobs in Arnold, MD (NOW HIRING)

Pharmaron

Clinical Informatics Specialist

Baltimore, MD · On-site +1

$24 - $30/hr

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

New

Global Alliant Inc

Clinical Analyst

Baltimore, MD · Remote

Remote Job Duration: Contract / FTE Client: Federal Criteria- Need US citizenship because of ... Clinical or healthcare educational background * ICD-10, CPT, HCPCS * Claims, denials, billing or ...

Global Alliant Inc

Clinical Analyst

Baltimore, MD · Remote

Remote JobDuration: Contract / FTE Client: Federal Criteria-Need US citizenshipbecause of federal ... Clinical or healthcare educational background * ICD-10, CPT, HCPCS * Claims, denials, billing or ...

All JobsClinical Informatics JobsRemote Clinical Informatics JobsRemote Clinical Informatics Jobs in Arnold, MD

Remote Clinical Informatics information

See Arnold, MD salary details

$50.7K

$101K

$160K

How much do remote clinical informatics jobs pay per year?

As of Aug 21, 2026, the average yearly pay for remote clinical informatics in Arnold, MD is $101,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,200.00 and $112,700.00 per year, depending on experience, location, and employer.

What is remote clinical informatics?

Remote clinical informatics is a field that involves managing and analyzing health information and data to improve patient care, with professionals working from locations outside traditional healthcare settings. These specialists use technology to collect, store, and interpret medical data, helping healthcare providers make better clinical decisions. Remote clinical informaticists often collaborate with IT teams, clinicians, and administrators to optimize electronic health records (EHRs), ensure data security, and support telehealth initiatives. This role is critical in the modern healthcare environment, where digital solutions and remote work are increasingly common.

What is a remote clinical informatics job?

Remote clinical informatics jobs include positions such as clinical informatics analyst, clinical informatics specialist, informatics programmer analyst, informatics scientist, and clinical informatics educator. Clinical informatics is the discipline of studying how technology can improve the flow of clinical and patient information between researchers, clinicians, patients, and health care organizations in the health care system. Your specific duties depend on your position, but most jobs require you to help design and develop data storage and sharing systems. Your responsibilities may also include helping to analyze and improve current informatics systems at an institution.

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

Remote Clinical Informatics professionals often work closely with both clinical staff and IT teams to optimize electronic health record (EHR) systems and ensure seamless health data workflows. They facilitate communication between clinicians and technical staff, translating clinical needs into technical requirements and vice versa. Regular virtual meetings, project management tools, and secure messaging platforms are commonly used to coordinate updates, solve problems, and implement new technologies. Strong collaboration skills are essential, as much of the work involves cross-functional teamwork to improve patient care and data integrity.

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

To thrive as a Remote Clinical Informatics Specialist, you need a background in healthcare, knowledge of clinical workflows, and often a degree in informatics, health information management, or a related field. Familiarity with electronic health records (EHR) systems, data analytics tools, and certifications such as Certified Professional in Healthcare Information and Management Systems (CPHIMS) are commonly required. Strong communication, problem-solving skills, and the ability to collaborate across clinical and technical teams are essential soft skills. These abilities are vital to ensure accurate data management, successful implementation of health IT solutions, and improved patient care outcomes in a remote environment.

What is the difference between Remote Clinical Informatics vs Remote Health Data Analyst?

AspectRemote Clinical InformaticsRemote Health Data Analyst
CredentialsHealthcare-related degrees, certifications like CPHIMS or CAHIMSData analysis or statistics degrees, certifications like CPC or CAP
Work EnvironmentHealthcare settings, hospitals, clinics, telehealthResearch institutions, healthcare organizations, consulting firms
Employer & IndustryHospitals, healthcare providers, EHR vendorsHealthcare analytics firms, insurance companies, research organizations
Search & Comparison IntentUnderstanding roles in healthcare IT, telehealth, clinical systemsAnalyzing healthcare data, reporting, and insights

Remote Clinical Informatics focuses on implementing and managing healthcare technology systems within clinical settings, requiring healthcare credentials. In contrast, Remote Health Data Analysts primarily analyze healthcare data to generate insights, often with a background in data analysis. Both roles support healthcare organizations but serve different functions in the industry.

Is a remote clinical informatics specialist in demand?

Remote clinical informatics specialists are in high demand due to the increasing adoption of electronic health records and healthcare data systems. Employers seek professionals skilled in health IT, data analysis, and interoperability to improve patient care and operational efficiency, often requiring certifications like CPHIMS or CAHIMS.

What can I do with a remote clinical informatics degree?

A remote clinical informatics degree prepares individuals for roles such as clinical informaticist, health IT analyst, or EHR implementation specialist. These positions involve managing healthcare data, optimizing electronic health record systems, and improving clinical workflows, often requiring knowledge of healthcare standards and certification in health informatics. Remote work allows flexibility in healthcare organizations, research institutions, and technology companies focused on health data solutions.
More about Remote Clinical Informatics jobs

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

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

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

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

Remote Clinical Informatics jobs near you
Infographic showing various Remote Clinical Informatics job openings in Arnold, MD as of July 2026, with employment types broken down into 66% Full Time, and 34% Contract. Highlights an 100% Remote job distribution, with an average salary of $101,047 per year, or $48.6 per hour.

Clinical Informatics Specialist

Pharmaron

Baltimore, MD • On-site, Remote

$24 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New

Job description

Position: Clinical Informatics Specialist

Salary Range: $24.00/hr. - $30.00/hr.

Location: Baltimore, MD (On-site / Hybrid / Remote)

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 www.pharmaron.com.

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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