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Drug Safety Jobs in Indiana (NOW HIRING)

micro1 AI

Pharmacovigilance Expert

South Bend, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Fishers, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Evansville, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Fort Wayne, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Carmel, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Indianapolis, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

Elanco

Product Safety Manager

Indianapolis, IN

Responsible for the preparation, interpretation and presentation of drug safety aggregate data reports, to internal and external customers and global regulatory authorities as required. * Leads or ...

micro1 AI

Clinical Pharmacy Technicians

Fort Wayne, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Clinical Pharmacy Technicians

Carmel, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Clinical Pharmacy Technicians

Fishers, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Clinical Pharmacy Technicians

Indianapolis, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Clinical Pharmacy Technicians

South Bend, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Clinical Pharmacy Technicians

Evansville, IN · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

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All JobsDrug Safety JobsDrug Safety Jobs in Indiana

Drug Safety information

See Indiana salary details

$10

$24

$35

How much do drug safety jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for drug safety in Indiana is $24.36, according to ZipRecruiter salary data. Most workers in this role earn between $21.25 and $27.21 per hour, depending on experience, location, and employer.

What is drug safety?

Drug safety, also known as pharmacovigilance, is the science and activities related to detecting, assessing, understanding, and preventing adverse effects or other drug-related problems. Professionals in drug safety monitor the safety profiles of medications, collect and analyze data on side effects, and help ensure that medicines are used safely and effectively. Their work is crucial for protecting public health and supporting regulatory compliance throughout a drug’s lifecycle.

What is the difference between Drug Safety vs Pharmacovigilance Specialist?

AspectDrug SafetyPharmacovigilance Specialist
Required CredentialsDegree in pharmacy, medicine, or life sciences; certifications like Drug Safety CertificationSimilar credentials; often the same certifications are required
Work EnvironmentPharmaceutical companies, CROs, regulatory agenciesSame as Drug Safety, often within the same teams
Industry UsageFocuses on monitoring and reporting adverse drug reactionsFocuses on detecting, assessing, and preventing adverse effects
Search & Comparison IntentOften compared for roles in drug safety monitoringSimilar roles, but with a focus on safety data analysis

Drug Safety and Pharmacovigilance Specialist roles are closely related, often overlapping in responsibilities and required qualifications. Both work within the pharmaceutical industry to ensure medication safety, but Drug Safety may emphasize reporting adverse events, while Pharmacovigilance focuses on analyzing safety data to prevent issues.

What are some common challenges faced by professionals in drug safety roles, and how can they be managed?

Professionals in Drug Safety often face challenges such as staying current with evolving regulatory requirements, managing large volumes of adverse event data, and ensuring timely reporting to health authorities. These challenges can be managed through continuous training, strong collaboration with cross-functional teams (such as clinical, regulatory, and medical affairs), and leveraging specialized safety databases and software. Additionally, clear communication and robust standard operating procedures help maintain compliance and data integrity in this dynamic work environment.

What are the key skills and qualifications needed to thrive in drug safety, and why are they important?

To thrive in Drug Safety, a strong background in life sciences, pharmacovigilance principles, and regulatory guidelines is essential, often supported by a relevant degree such as pharmacy, nursing, or life sciences. Familiarity with safety databases (like Argus or ARISg), MedDRA coding, and certifications such as RAPS or DIA are commonly required. Attention to detail, analytical thinking, and clear communication skills help professionals accurately evaluate data and collaborate across teams. These competencies are crucial for ensuring patient safety, regulatory compliance, and effective risk management throughout the drug lifecycle.
What are the most commonly searched types of Drug Safety jobs in Indiana? The most popular types of Drug Safety jobs in Indiana are:
What are popular job titles related to Drug Safety jobs in Indiana? For Drug Safety jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Drug Safety jobs in Indiana look for? The top searched job categories for Drug Safety jobs in Indiana are:
What cities in Indiana are hiring for Drug Safety jobs? Cities in Indiana with the most Drug Safety job openings:
Drug Safety jobs near you
Infographic showing various Drug Safety job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $50,674 per year, or $24.4 per hour.

Pharmacovigilance Expert

micro1 AI

South Bend, IN • Remote

$70 - $80/hr

Part-time

Posted 6 days ago

Job description

Role Title: Pharmacovigilance Expert


Role Type: Contractor


Location: Remote


micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. 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. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.


Scope of Work

  1. Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
  2. Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
  3. Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
  4. Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
  5. Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
  6. Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.


Preferred Qualifications

  1. 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
  2. Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
  3. Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
  4. Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
  5. Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
  6. Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
  7. Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.

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