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Remote Irb Analyst Jobs (NOW HIRING)

Clinical Contracts Analyst (REMOTE)

Boston, MA · On-site +1

$75K - $90K/yr

... IRB oversight, and other reimbursable costs for clinical trials. • Manage contractual and ... analytics, reporting, and business intelligence support for clinical trials. • Track timelines ...

Clinical Contracts Analyst (REMOTE)

Boston, MA · Remote

$75K - $90K/yr

... fees, IRB oversight, and other reimbursable costs for clinical trials. Manage contractual and ... Provide data management, analytics, reporting, and business intelligence support for clinical ...

Clinical Research Associate

Boston, MA · On-site +1

$20.16 - $29.01/hr

... analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching ... This position involves working with clinical teams, Institutional Review Boards (IRB), clinical ...

Clinical Research Associate

Boston, MA · Remote

$20.16 - $29.01/hr

... analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching ... This position involves working with clinical teams, Institutional Review Boards (IRB), clinical ...

$105K - $135K/yr

Remote (U.S.) with periodic travel - Personnel may perform work remotely from their residence ... Support execution of IRB-approved research protocols. * Conduct advanced audiometric and functional ...

Research Audiologist

$105K - $135K/yr

Remote (U.S.) with periodic travel - Personnel may perform work remotely from their residence ... Support execution of IRB-approved research protocols. * Conduct advanced audiometric and functional ...

... analyses, and recommendations for ongoing and proposed human performance research * Utilize ... IRB, HRPO, IACUC, IBC, MOU, and data-sharing agreements, while ensuring compliance through audit ...

... analytical solutions -we are modernizing clinical trials and accelerating the development of life ... Independently completes IRB/EC submissions for sites or submits to central IRB/EC on behalf of the ...

$15/hr

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Conduct descriptive analysis of pre/post data and produce clear tables, charts, and summaries.

New

Remote Schedule: Full-time, 8am - 5pm EST Monday - Friday Salary Range: 58,600.00 - 85,000.00 ... Conduct initial IRB and PRA/OMB screening for research-like activities and prepare documentation ...

Showing results 21-40

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.

More about Remote Irb Analyst jobs

What cities are hiring for Remote Irb Analyst jobs?

Cities with the most Remote Irb Analyst job openings:

What are the most commonly searched types of Irb Analyst jobs?

The most popular types of Irb Analyst jobs are:

What states have the most Remote Irb Analyst jobs?

States with the most job openings for Remote Irb Analyst jobs include:

Infographic showing various Remote Irb Analyst job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, and 9% Contract. Highlights an 100% Remote job distribution.

Clinical Contracts Analyst (REMOTE)

Teleflex

Boston, MA • On-site, Remote

$75K - $90K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.


Teleflex rating

8.3

Company rating: 8.3 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Expected Travel: Up to 25%
Requisition ID: 13966
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Interventional - The Interventional business unit at Teleflex develops innovative medical devices used to diagnose and treat coronary and peripheral vascular diseases. We focus strategically on coronary and peripheral interventions, vascular and bone access, and large-bore closure solutions.
Our portfolio includes a broad range of clinically relevant products, such as the GuideLiner™ and Turnpike™ Catheters; the Orsiro™ Mission™ Drug-Eluting Stent; the PK Papyrus™ Covered Coronary Stent; the Ringer™ Perfusion Balloon Catheter; the Pulsar™ -18 T3 Self-Expanding Stent; Passeo™ Balloon Catheters; and the OnControl™ Powered Bone Access System.
Backed by a strong R&D pipeline, our rapidly growing Interventional business unit is well positioned to continue advancing new technologies that support the treatment of critically ill patients. Join a dynamic team dedicated to delivering innovative medical solutions that make a meaningful difference in patients' lives.
Position Summary
The Clinical Contracts Analyst will develop and negotiate contracts and budgets associated with clinical trials, ensure contracts comply with regulations, manage the lifecycle of contracts, and process clinical trial payments.
Principal Responsibilities
• Facilitate negotiation, execution, and ongoing revisions of clinical study contracts based on substantial knowledge of financial/fair market value, regulatory, and clinical requirements while demonstrating clinical knowledge. Recommend new/or revised language for contract templates.
• Function as the primary internal and external contact for contracts and payments.
• Assure compliance with existing agreements and analyze the need for contract amendments or renewals, and make recommendations, and/or negotiate changes to terms and conditions.
• Facilitate and direct internal legal review of contract language as appropriate.
• Maintain contract negotiation correspondence and agreements in accordance with procedures.
• Monitor changes to regulatory and legal requirements affecting clinical study contracts and reimbursement practices, in coordination with Legal and Regulatory.
• Provide proper escalation of contractual and payment issues and actively engage with management to provide recommendations for mitigation.
• Manage the clinical compensation process, database, and related reporting, including issuance of payments for investigator fees, IRB oversight, and other reimbursable costs for clinical trials.
• Manage contractual and financial information in clinical trial databases with a high degree of accuracy.
• Provide data management, analytics, reporting, and business intelligence support for clinical trials.
• Track timelines and ensure contract and compensation requirements are met in coordination with project team expectations.
• Develop a study compensation agreement template with support from project managers and management and obtain necessary approvals.
• Ensure consistency with the study protocol, clinical contract template, informed consent language, and compensation agreement.
• Collaborate with project team members on the development and testing of study payment programming
• Interface with Finance and Accounts Payable as needed on payment inquiries.
• Regularly communicate contract and/or compensation agreement negotiation and execution status to the project team and clinical management.
• Develop and/or negotiate investigator-initiated research contracts, data use agreements, third-party vendor clinical research contracts, and clinical consulting agreements upon request.
• Perform other duties as assigned.
• Identify opportunities for process improvement in collaboration with cross-functional teams; present and implement process improvement plans to management and/or key stakeholders.
Education / Experience Requirements
• BS/BA in a related field or equivalent experience.
• Experience in clinical research and related regulatory requirements.
• Minimum of five years' experience in contract negotiation/administration and financial tracking/analysis against contracts.
• Clinical contract work experience from pharmaceutical, medical device, healthcare, or Contract Research Organizations (preferred).
• Experience with contractual agreements, including master services agreements (MSAs), statements of work (SOWs), data use agreements (DUA), non-disclosure agreements (NDAs), and amendments.
Specialized Skills / Other Requirements
• Understanding of regulatory requirements (e.g., CFR, GCP) and documents.
• Moderate knowledge of the clinical research process, medical terminology, and healthcare compliance and privacy regulations pertaining to legal studies (e.g., HIPAA and Sunshine Act).
• Proven expertise in Microsoft Office Suite, including Word, PowerPoint, Access, Excel, and SharePoint, and electronic data capture.
• Basic understanding of relational databases, including query design, file manipulation, and table structure.
• Ability to work in a team environment and represent the organization on specific projects.
• Advanced written and verbal communication skills and interpersonal relationship skills.
• Proven problem-solving, organizational, analytical, and critical thinking skills.
• Ability to work independently, prioritize, and work within a matrix team environment is essential.
CULTURE:
• Customer Experience - Representing Teleflex in a customer-facing position is a tremendous responsibility and opportunity. All CMA colleagues are expected to perform with the highest levels of professionalism, service, and ethics in order to strengthen the Teleflex brand and relationship with our customers.
• Continuous Improvement - Demonstrates initiative and critical thinking to identify and prioritize process and performance gaps. Develops solutions to deliver improved results. Exemplifies continuous improvement of thought processes and focus.
• Culture and Values - Exemplifies Teleflex values and ensures a fair, open, and productive climate that is engaging, ethical, and legally compliant. Strives to work effectively across boundaries in a complex matrix environment. Lead and participate in the process of promotional and other materials, working
internally and cross-functionally to ensure materials are processed completely, based on an accurate interpretation of clinical practice and data.
TRAVEL REQUIRED: 20% (Domestically and Internationally)
The pay range for this position at commencement of employment is expected to be between $79,400- $119,100; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental, and vision insurance, flexible spending accounts, participation in a 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability, and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.
If hired, the 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.
#LI-LM1
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

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