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Medical Safety Manager Jobs in Boca Raton, FL (NOW HIRING)

micro1 AI

Medical Writing Manager

Coral Springs, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Sunrise, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Fort Lauderdale, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Miramar, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Pembroke Pines, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Davie, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Hollywood, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Plantation, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Pompano Beach, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Boca Raton, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

West Palm Beach, FL · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

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Showing results 41-60

All JobsMedical Safety JobsMedical Safety Manager JobsMedical Safety Manager Jobs in Boca Raton, FL

Medical Safety Manager information

See Boca Raton, FL salary details

$30.4K

$93.2K

$148K

How much do medical safety manager jobs pay per year?

As of Aug 16, 2026, the average yearly pay for medical safety manager in Boca Raton, FL is $93,178.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $110,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical safety manager?

To thrive as a Medical Safety Manager, you need a strong background in pharmacovigilance, clinical research, and regulatory compliance, often supported by a degree in pharmacy, medicine, or life sciences. Familiarity with safety databases (such as Argus or ARISg), MedDRA coding, and global regulatory reporting systems is essential. Excellent analytical thinking, attention to detail, and effective communication skills set outstanding professionals apart in this field. These skills and qualities are crucial for ensuring drug safety, regulatory adherence, and protecting patient well-being throughout clinical development and post-marketing surveillance.

How does a medical safety manager typically collaborate with cross-functional teams during the drug development process?

Medical Safety Managers play a central role in ensuring patient safety by working closely with teams such as clinical research, regulatory affairs, pharmacovigilance, and medical affairs. They regularly participate in multidisciplinary meetings to review safety data, assess risk, and implement mitigation strategies. Their collaboration ensures that safety concerns are addressed promptly and that regulatory submissions reflect the most up-to-date safety profiles. Effective communication and coordination with these teams are essential for successful product development and compliance with industry standards.

What does a medical safety manager do?

A Medical Safety Manager is responsible for overseeing the safety of pharmaceutical products throughout their lifecycle. They analyze and evaluate data related to adverse drug reactions, ensure compliance with regulatory requirements, and implement risk management strategies. Medical Safety Managers work closely with clinical teams, regulatory authorities, and healthcare professionals to monitor, assess, and report on drug safety. Their work is critical in ensuring that medicines are safe for patients and that any potential risks are identified and managed appropriately.

What is the difference between Medical Safety Manager vs Medical Safety Specialist?

AspectMedical Safety ManagerMedical Safety Specialist
CertificationsMedical Safety Certification, Pharmacovigilance trainingMedical Safety Certification, Pharmacovigilance training
Work EnvironmentLeads safety teams, manages safety programsSupports safety activities, conducts case assessments
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical companies, clinical research organizations

The Medical Safety Manager and Medical Safety Specialist roles share similar certifications and work environments within the pharmaceutical industry. The manager oversees safety programs and teams, while the specialist focuses on case assessments and support tasks. Both roles are essential for ensuring drug safety and compliance.

What cities near Boca Raton, FL are hiring for Medical Safety Manager jobs?

Cities near Boca Raton, FL with the most Medical Safety Manager job openings:

Medical Safety Manager jobs near you
Infographic showing various Medical Safety Manager job openings in Boca Raton, FL as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $93,178 per year, or $44.8 per hour.

Medical Writing Manager

micro1 AI

Coral Springs, FL • Remote

$50 - $80/hr

Part-time

Posted 12 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply