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Drug Safety Associate Jobs in Alaska (NOW HIRING)

micro1 AI

Pharmacovigilance Expert

Anchorage, AK · 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 ...

Fred Meyer

DRUG-GEN MDSE/LEAD CLERK

Anchorage, AK · On-site

$15.75 - $19.50/hr

Drug GM experience * Retail experience * Second language (speaking, reading and/or writing ... associates on inventory/stocking and Computer Assisted Ordering. * Reinforce safety programs by ...

lynden

Safety Manager

Anchorage, AK · On-site

$74K - $94K/yr

Manage the company's drug and alcohol testing program, including pre-employment, random, post ... Associate degree from a two-year college or technical school, or an equivalent combination of ...

lynden

Safety Manager

Anchorage, AK · On-site

$74K - $94K/yr

Manage the company's drug and alcohol testing program, including pre-employment, random, post ... Associate degree from a two-year college or technical school, or an equivalent combination of ...

Fred Meyer

DRUG-GEN MDSE/CLERK

Fairbanks, AK

$17 - $22.75/hr

Embrace the Customer 1st strategy and encourage associates to deliver excellent customer service ... Reinforce safety programs by complying with safety procedures and identify unsafe conditions and ...

Fred Meyer

DRUG-GEN MDSE/CLERK

Fairbanks, AK · On-site

$17.50 - $23.50/hr

Embrace the Customer 1st strategy and encourage associates to deliver excellent customer service ... safety of others. Based in Portland, Oregon, Fred Meyer merged with The Kroger Company in 1998.

Akima, LLC

Safety Coordinator

Anchorage, AK · On-site

Associate or Bachelor's degree in Occupational Safety, Environmental Science, or related field ... Must receive a favorable background check and drug testing results. * Basic proficiency in the ...

MV Transportation

Safety Manager

Anchorage, AK · On-site

Lead Safety. Drive Excellence. MV Transportation is seeking an experienced Safety Manager to lead ... drug test and background check after receiving a conditional offer of employment. #appcast

MV Transportation

Safety Manager

Anchorage, AK · On-site

Lead Safety. Drive Excellence. MV Transportation is seeking an experienced Safety Manager to lead ... drug test and background check after receiving a conditional offer of employment. #appcast

MV Transportation

Safety Manager

Anchorage, AK · On-site

Responsibilities Lead Safety. Drive Excellence. MV Transportation is seeking an experienced Safety ... drug test and background check after receiving a conditional offer of employment. #appcast

MV Transportation

Safety Manager

Anchorage, AK

Responsibilities Lead Safety. Drive Excellence. MV Transportation is seeking an experienced Safety ... drug test and background check after receiving a conditional offer of employment. #appcast ...

Searhc

Safety Officer

Juneau, AK · On-site

Pay Range:$31.83 - $44.56 Manages day-to-day functions, as directed by the Director of Safety, associated with the overall SEARHC Safety Program. The position is responsible for ensuring a ...

Hawk Group

Safety Specialist

Anchorage, AK · On-site

The Safety Specialist operates in collaboration with other Environmental, Health, and Security staff, but functionally reports to the Safety Manager to ensure activities are in adherence to Client ...

Donlin Gold LLC

Health & Safety Manager

Anchorage, AK · On-site

$225K - $250K/yr

Reporting to the General Manger, the Health & Safety Manager is responsible for the development ... A post-offer criminal background clearance, physical and drug screening are required. Open until ...

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All JobsDrug Safety Associate JobsDrug Safety Associate Jobs in Alaska

Drug Safety Associate information

See Alaska salary details

$13

$52

$92

How much do drug safety associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for drug safety associate in Alaska is $52.92, according to ZipRecruiter salary data. Most workers in this role earn between $41.44 and $59.81 per hour, depending on experience, location, and employer.

How does a drug safety associate typically collaborate with other teams during the drug development process?

Drug Safety Associates regularly work in close coordination with clinical research, regulatory affairs, and medical affairs teams. They are responsible for collecting, evaluating, and reporting adverse event data, which often requires clear communication with clinical trial staff and investigators. Additionally, they may participate in cross-functional safety review meetings to discuss safety findings and ensure compliance with regulatory requirements. This collaborative environment helps ensure comprehensive safety monitoring throughout the drug's lifecycle.

What does a drug safety associate do?

A drug safety associate works in the medical industry to monitor the safety of pharmaceutical drugs and to evaluate and prevent adverse reactions in patients. A career in drug safety, also called pharmacovigilance, can include work with clinical research organizations that conduct trials, biotechnology firms, pharmaceutical companies, or government agencies like the National Institutes of Health (NIH). Drug safety associates need excellent research skills, a strong background in medical or biological science, and in-depth knowledge of the Food and Drug Administration (FDA) regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether specific pharmaceutical drugs are safe.

What is a drug safety associate?

Drug Safety Associates are professionals responsible for monitoring and evaluating the safety of pharmaceutical products. They collect, analyze, and report data on adverse drug reactions to ensure compliance with regulatory requirements and to protect patient safety. Their work involves reviewing case reports, maintaining safety databases, and communicating safety information to regulatory agencies and healthcare professionals. Drug Safety Associates play a vital role in the pharmacovigilance process throughout the lifecycle of a drug.

What is the difference between Drug Safety Associate vs Pharmacovigilance Specialist?

AspectDrug Safety AssociatePharmacovigilance Specialist
CredentialsTypically requires a degree in life sciences or healthcare, with certifications like PV or drug safety trainingSimilar credentials, often with additional certifications or experience in pharmacovigilance
Work EnvironmentPharmaceutical companies, CROs, or healthcare settings focusing on safety data managementSame as Drug Safety Associate, often with more specialized pharmacovigilance tasks
Employer & IndustryPharmaceutical, biotech, and healthcare industriesSame industries, with a focus on drug safety monitoring and compliance

Both roles involve monitoring drug safety data, reporting adverse events, and ensuring regulatory compliance. The main difference lies in the scope and specialization, with Pharmacovigilance Specialists often handling more complex safety data analysis and regulatory submissions. However, the roles overlap significantly, and job titles are sometimes used interchangeably depending on the organization.

What are the key skills and qualifications needed to thrive as a Drug Safety Associate, and why are they important?

To thrive as a Drug Safety Associate, you need a solid background in life sciences or pharmacy, knowledge of pharmacovigilance principles, and attention to detail. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and regulatory reporting systems is typically required. Strong organizational skills, effective communication, and the ability to work under deadlines help you excel in collaborating with cross-functional teams. These skills ensure accurate adverse event reporting, regulatory compliance, and protection of patient safety throughout the drug development lifecycle.
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Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in Alaska as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $110,082 per year, or $52.9 per hour.

Pharmacovigilance Expert

micro1 AI

Anchorage, AK • 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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