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Drug Safety Manager Jobs in Spring, TX (NOW HIRING)

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and ...

The Field Safety Manager (FSM) collaborates with employees and managers across all areas of safety ... AmeriGas is a Drug Free Workplace. Candidates must be willing to submit to a pre-employment drug ...

The Field Safety Manager (FSM) collaborates with employees and managers across all areas of safety ... AmeriGas is a Drug Free Workplace. Candidates must be willing to submit to a pre-employment drug ...

ZACHRY is dedicated to providing a Safe and Drug-Free work environment and is an Equal Opportunity ... Work with Management regarding regulatory complaints. Work with the Corporate Safety Support Staff ...

New

... Drug and Alcohol Policy. Assure Project Line Management is kept in the decision-making process. • Coordinate and assist in safety evaluation as deemed necessary. • To interface, provide guidance ...

New

Honeywell Safety Manager Lead

Houston, TX · On-site

$130K - $150K/yr

Safety within control system application * Strong/ clear written and verbal communication skills ... Must pass background check/ drug screen * 4 years - Programming and support of Honeywell DCS and ...

Able to work in a fast-paced environment and to manage emergency situations. * Strong skills with ... drug test and background check after receiving a conditional offer of employment.

Able to work in a fast-paced environment and to manage emergency situations. * Strong skills with ... drug test and background check after receiving a conditional offer of employment.

Able to work in a fast-paced environment and to manage emergency situations. * Strong skills with ... employment drug test and background check after receiving a conditional offer of employment.

Honeywell Safety Manager Lead

Houston, TX · On-site

$130K - $150K/yr

Safety within control system application * Strong/ clear written and verbal communication skills ... Must pass background check/ drug screen * 4 years - Programming and support of Honeywell DCS and ...

Implements, administers and maintains project Drug and Alcohol Substance Abuse Program. Develops ... Manages construction contractor safety and health program administration. Administers project ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and ...

Showing results 21-40

Drug Safety Manager information

See Spring, TX salary details

$32.9K

$76.5K

$121.5K

How much do drug safety manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for drug safety manager in Spring, TX is $76,505.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,300.00 and $91,200.00 per year, depending on experience, location, and employer.

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

AspectDrug Safety ManagerPharmacovigilance Specialist
CredentialsTypically requires a degree in pharmacy, life sciences, or related field; certifications like PV or REMS are commonSimilar educational background; often holds certifications in pharmacovigilance or drug safety
Work EnvironmentLeads drug safety teams, manages safety data, and oversees compliance within pharmaceutical companiesFocuses on collecting, analyzing, and reporting safety data, often working under supervision
Industry UsageUsed in pharmaceutical and biotech companies for overseeing safety programsCommonly used in regulatory agencies and contract research organizations

While both roles involve drug safety and require similar qualifications, the Drug Safety Manager typically has a leadership role overseeing safety operations, whereas the Pharmacovigilance Specialist focuses on data collection and analysis. The manager has broader responsibilities, including team management and strategic planning.

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

To thrive as a Drug Safety Manager, you need expertise in pharmacovigilance, regulatory compliance, and drug safety reporting, typically backed by a degree in pharmacy, life sciences, or a related field. Familiarity with safety databases (such as Argus or ARISg), MedDRA coding, and ICH-GCP guidelines is commonly required, along with relevant certifications like those from the Drug Information Association (DIA). Strong analytical thinking, attention to detail, and effective communication skills are crucial for managing safety data and collaborating with cross-functional teams. These skills ensure accurate safety monitoring, regulatory adherence, and the protection of patient well-being throughout a drug’s lifecycle.

What are the main challenges drug safety managers face when ensuring compliance with global pharmacovigilance regulations?

Drug Safety Managers often navigate complex and evolving international regulations to ensure a company's pharmacovigilance practices are compliant. They must coordinate with cross-functional teams to gather timely and accurate safety data, manage case processing workflows, and prepare regulatory submissions under strict deadlines. Staying updated on changing global requirements and aligning internal processes accordingly can be challenging, but is crucial for patient safety and product success. Effective communication, attention to detail, and proactive risk management are key in overcoming these challenges.

What does a drug safety manager do?

A Drug Safety Manager is responsible for overseeing the collection, evaluation, and reporting of data related to the safety of pharmaceutical products. They ensure compliance with regulatory requirements and help identify, assess, and mitigate risks associated with medications. Their role often includes managing a team, developing safety protocols, and communicating findings to regulatory authorities and internal stakeholders. By maintaining vigilance over drug safety, they help protect patient health and support the ongoing improvement of pharmaceutical products.
What are the most commonly searched types of Drug Safety jobs in Spring, TX? The most popular types of Drug Safety jobs in Spring, TX are:
What are popular job titles related to Drug Safety Manager jobs in Spring, TX? For Drug Safety Manager jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Drug Safety Manager jobs in Spring, TX look for? The top searched job categories for Drug Safety Manager jobs in Spring, TX are:
What cities near Spring, TX are hiring for Drug Safety Manager jobs? Cities near Spring, TX with the most Drug Safety Manager job openings:
Infographic showing various Drug Safety Manager job openings in Spring, TX 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 $76,505 per year, or $36.8 per hour.

Pharmacovigilance Expert

micro1 AI

Houston, TX • 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.