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Remote Medical Alert Systems Jobs in Boston, MA (NOW HIRING)

37554294 Remote Medical Writer, 7 Months Contract Sigma Systems is currently looking for a Remote Medical Writer The Medical Writer is responsible for authoring, reviewing, and coordinating the ...

Software Engineer

Boston, MA · On-site +1

$110 - $125K/hr

About Spoiler Alert Spoiler Alert is a CPG and retail tech company on a mission to expand consumer ... Participate in shared support duties and help maintain the reliability of our systems Collaborate ...

Medical Coder - Remote

Boston, MA · Remote

$50 - $80/hr

Remote Job Overview We are seeking experienced Medical Coders to contribute their healthcare coding expertise to an innovative project focused on improving next-generation AI systems. In this role ...

Medical Coder - Remote

Boston, MA · Remote

$50 - $80/hr

Remote Job Overview We are seeking experienced Medical Coders to contribute their healthcare coding expertise to an innovative project focused on improving next-generation AI systems. In this role ...

Medical Auditor Job Type: Contractor Location: Remote Job Overview We are seeking experienced ... In this role, you will help improve next-generation AI systems by reviewing, evaluating, and ...

Medical Auditor Job Type: Contractor Location: Remote Job Overview We are seeking experienced ... In this role, you will help improve next-generation AI systems by reviewing, evaluating, and ...

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Remote Medical Alert Systems information

See Boston, MA salary details

$18

$23

$25

How much do remote medical alert systems jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for remote medical alert systems in Boston, MA is $23.36, according to ZipRecruiter salary data. Most workers in this role earn between $19.57 and $24.81 per hour, depending on experience, location, and employer.

What is the difference between Remote Medical Alert Systems vs Medical Call Center Agents?

AspectRemote Medical Alert SystemsMedical Call Center Agents
CredentialsMinimal; often includes basic trainingOften requires certifications in healthcare or communication
Work EnvironmentHome-based or remote setupCall centers or remote offices
Industry UsageHealthcare, senior care, emergency responseHealthcare, customer service, telehealth
Job FocusMonitoring and alerting for emergenciesHandling calls, providing information, support

Remote Medical Alert Systems primarily focus on providing emergency alerts and monitoring for seniors or at-risk individuals, often working remotely with minimal credentials. Medical Call Center Agents handle a broader range of healthcare-related calls, requiring more certifications and working in call centers or remotely. Both roles are vital in healthcare communication but differ in scope and work environment.

What are popular job titles related to Remote Medical Alert Systems jobs in Boston, MA?

For Remote Medical Alert Systems jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Remote Medical Alert Systems jobs in Boston, MA look for?

The top searched job categories for Remote Medical Alert Systems jobs in Boston, MA are:

What cities near Boston, MA are hiring for Remote Medical Alert Systems jobs?

Cities near Boston, MA with the most Remote Medical Alert Systems job openings:

Infographic showing various Remote Medical Alert Systems job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $48,588 per year, or $23.4 per hour.

Medical Writer

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

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


Job description

37554294 Remote Medical Writer, 7 Months Contract
Sigma Systems is currently looking for a Remote Medical Writer
The Medical Writer is responsible for authoring, reviewing, and coordinating the development of high-quality clinical and regulatory documents that support global clinical development programs. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans

Responsibilities:

  • Author, edit, and review clinical and regulatory documents, including:
    • Clinical study protocols and protocol amendments
    • Investigator Brochures (IBs)
    • Clinical Study Reports (CSRs)
    • Briefing Book support
    • IND and NDA summary documents and other regulatory submission materials
  • Develop documents that are consistent with regulatory requirements, internal standards, and medical writing plans, while supporting the overall clinical development lifecycle and program objectives for one or more clinical development programs.
  • Collaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents.
  • Negotiate document deliverable milestones and timelines with cross-functional teams to ensure alignment across functions and adherence to medical writing plans and program objectives.
  • Facilitate document review cycles, resolve reviewer comments, and drive consensus among stakeholders while maintaining quality and schedule commitments.
  • Ensure documentation complies with applicable regulatory guidance, Good Clinical Practice (GCP), company standards, and industry best practices.
  • Contribute to the development and continuous improvement of medical writing processes, templates, style guides, and operational procedures.
  • Support regulatory submissions, health authority interactions, and inspection readiness activities as needed

Core Competencies

  • Scientific and regulatory writing expertise
  • Project and timeline management
  • Cross-functional collaboration and influence
  • Strategic thinking and problem solving
  • Attention to quality and regulatory compliance
  • Effective communication and stakeholder management

Requirements:

  • Advanced degree Bachelor's degree or more.
  • Experience authoring clinical and regulatory documents within the pharmaceutical, biotechnology, or clinical research industry.
  • Strong knowledge of clinical development, regulatory requirements, and applicable guidance documents (e.g., ICH guidelines).
  • Excellent scientific writing, editing, and communication skills.
  • Demonstrated ability to manage multiple projects and negotiate timelines in a cross-functional environment.

Strong organizational skills, attention to detail, and ability to work independently and collaboratively