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Remote Irb Analyst Jobs in Timonium, MD (NOW HIRING)

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Remote Irb Analyst information

What is a remote IRB analyst?

Remote IRB analysts are professionals who review research proposals to ensure they comply with ethical standards and federal regulations, working from a remote location rather than on-site. They are responsible for evaluating study protocols, informed consent documents, and safeguarding the rights and welfare of research participants. Remote IRB analysts typically collaborate with researchers, institutional review boards, and regulatory bodies via digital platforms. This role requires strong attention to detail, knowledge of ethical guidelines, and effective communication skills.

What are the key skills and qualifications needed to thrive as a remote IRB analyst?

To thrive as a Remote IRB Analyst, you need a solid understanding of federal regulations, ethical principles in human subjects research, and experience with IRB processes, often supported by a relevant degree. Familiarity with electronic IRB management systems and certifications such as CIP (Certified IRB Professional) are commonly required. Excellent organizational skills, attention to detail, and strong written communication are essential soft skills for this role. These competencies ensure ethical compliance, efficient review processes, and effective collaboration in protecting research participants.

How does a remote IRB analyst typically collaborate with research teams and other stakeholders?

As a Remote IRB Analyst, you will regularly interact with research coordinators, principal investigators, and institutional officials primarily through virtual meetings, email, and specialized IRB management platforms. Clear communication and timely feedback are essential, as you’ll review research protocols, provide guidance on regulatory compliance, and address queries about ethical standards. Successful analysts proactively coordinate with team members to resolve issues, ensure documentation accuracy, and maintain workflow efficiency, despite working from different locations.

What is the difference between Remote Irb Analyst vs Remote Clinical Research Coordinator?

AspectRemote Irb AnalystRemote Clinical Research Coordinator
Required CredentialsIRB certification, research ethics knowledgeClinical research experience, sometimes certifications
Work EnvironmentRemote, primarily administrative and review tasksRemote or onsite, coordinating clinical trial activities
Employer & IndustryResearch institutions, biotech, pharmaHospitals, research sites, pharma companies
Common Search & ComparisonYesYes

The Remote Irb Analyst primarily reviews and approves research protocols to ensure ethical compliance, requiring IRB certification. In contrast, the Remote Clinical Research Coordinator manages trial logistics and participant coordination. Both roles are essential in clinical research but differ in responsibilities and focus areas.

What are popular job titles related to Remote Irb Analyst jobs in Timonium, MD?

For Remote Irb Analyst jobs in Timonium, MD, the most frequently searched job titles are:

What job categories do people searching Remote Irb Analyst jobs in Timonium, MD look for?

The top searched job categories for Remote Irb Analyst jobs in Timonium, MD are:

Remote Irb Analyst jobs near you
Infographic showing various Remote Irb Analyst job openings in Timonium, MD as of August 2026, with employment types broken down into 84% Full Time, and 16% Part Time. Highlights an 100% Remote job distribution.

Clinical Informatics Specialist

Pharmaron

Baltimore, MD

$24 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 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 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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