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Drug Safety Consultant Jobs (NOW HIRING)

HB NEXT

Safety Consultant

Lawrenceville, GA · On-site

HB NEXT is seeking an experienced Safety Consultant to join our growing team in the Atlanta area ... Ability to pass a drug screen and 15-year background check What We Offer * Competitive salary

Puget Sound Energy

Safety Consultant

Goldendale, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

Puget Sound Energy

Safety Consultant

Longview, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

Puget Sound Energy

Safety Consultant

Bellevue, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

Puget Sound Energy

Safety Consultant

Bellevue, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

Puget Sound Energy

Safety Consultant

Ellensburg, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

Puget Sound Energy

Safety Consultant

Bellevue, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

Puget Sound Energy

Safety Consultant

Chehalis, WA · On-site

The Safety Health Work Practice Consultant works as a member of the corporate safety team to ... to pre-employment drug screening that includes screening for the presence of marijuana and ...

SEE Inc

Be Seen First

Entry Level Safety Consultant

Keedysville, MD · On-site

$30K - $45K/yr

Our Safety Consulting firm has been serving the Maryland, Virginia, DC area since 1992 . We ... Must be able to pass drug screen as well as background checks. Construction background is a major ...

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All JobsDrug Safety Consultant Jobs

Drug Safety Consultant information

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How much do drug safety consultant jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for drug safety consultant in the United States is $40.91, according to ZipRecruiter salary data. Most workers in this role earn between $33.17 and $48.08 per hour, depending on experience, location, and employer.

What does a drug safety consultant do?

A Drug Safety Consultant is responsible for monitoring, evaluating, and managing the safety of pharmaceutical products throughout their lifecycle. This professional analyzes data on adverse drug reactions, ensures compliance with regulatory requirements, and provides guidance on risk management strategies. Their work helps pharmaceutical companies maintain high safety standards and meet global regulatory obligations, ultimately protecting patient health. Drug Safety Consultants often collaborate with medical, regulatory, and clinical teams to ensure accurate and timely reporting of safety information.

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

To thrive as a Drug Safety Consultant, you need a solid background in pharmacovigilance, regulatory compliance, and clinical pharmacology, usually supported by a relevant degree in pharmacy, life sciences, or medicine. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and industry certifications like DSI or relevant GVP training is highly valuable. Strong analytical thinking, attention to detail, and effective communication skills help you excel in cross-functional teams and client interactions. These competencies are essential to ensure compliance, safeguard patient safety, and deliver high-quality drug safety services.

How does a drug safety consultant typically collaborate with cross-functional teams in the pharmaceutical industry?

As a Drug Safety Consultant, you will work closely with cross-functional teams such as clinical research, regulatory affairs, medical affairs, and data management. This collaboration is essential for ensuring the accurate reporting and analysis of adverse drug reactions and for meeting regulatory compliance requirements. Regular meetings, data-sharing, and joint problem-solving are common, allowing you to contribute your expertise in pharmacovigilance while gaining broader industry insights. Effective communication and teamwork are key to successfully navigating project timelines and regulatory submissions.

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

AspectDrug Safety ConsultantPharmacovigilance Specialist
Required CredentialsTypically requires life sciences degree, pharmacovigilance training, and industry certificationsSimilar credentials, often including pharmacovigilance training and relevant certifications
Work EnvironmentConsults for multiple clients or companies, often in a contract or freelance capacityWorks within pharmaceutical or biotech companies, focusing on internal safety processes
Employer & Industry UsageUsed by consulting firms, CROs, and pharmaceutical companiesPrimarily employed by pharmaceutical and biotech companies

Both roles require similar qualifications and focus on drug safety, but Drug Safety Consultants typically work independently or as contractors across various organizations, while Pharmacovigilance Specialists are usually employed directly by pharmaceutical companies to manage internal safety activities.

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Drug Safety Consultant jobs near you
Infographic showing various Drug Safety Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $85,098 per year, or $40.9 per hour.

PV Drug Safety Consultant

IntelliPro Group Inc.

Cambridge, MA • On-site

Contractor

Posted 11 days ago

Job description

Job Title: PV Drug Safety Consultant
Location: Hybrid – Cambridge, MA 02142
Duration: 09/21/2026 to 09/20/2027 with possible extension
Pay rate: $79.58/hr. on W2
Job Description:
The PV Aggregate Reports Scientist is part of the Safety Surveillance and Aggregate (SSA) Reports team and is responsible for managing the processes for all aggregate reports (PSURs, DSURs, PADERs, and local reports).
In this role, you will:
  • Serve as a subject matter expert on worldwide aggregate reporting safety requirements for the PV Scientist team, Safety, and cross-functional partners.
  • Respond to safety questions from internal and external stakeholders while reviewing and supporting the authoring of medical and scientific safety information.
  • Work closely with vendors, vendor oversight, and Quality Management teams to ensure high-quality standards across PV documents.
  • Support process improvement initiatives in collaboration with PV Sciences and cross-functional groups to develop, implement, and maintain compliant, efficient, and consistent global PV processes.

Key Responsibilities:
  • Aggregate Report Management: Lead and conduct all aspects of substantive projects, including the authoring and project management of PSURs, DSURs, PADERs, and local reports independently or collaboratively.
  • Subject Matter Expertise: Act as an expert on relevant safety requirements, company policies, and aggregate reporting knowledge; represent and articulate processes in cross-Safety and cross-functional forums.
  • Schedule & Regulatory Oversight: Support the Aggregate Reports Master Schedule (production, updates, stakeholder reviews), conduct worldwide legislation reviews for aggregate reporting, and provide impact assessments.
  • Health Authority Responses: Support authoring responses to safety inquiries from regulatory authorities alongside PV Scientists and key stakeholders.
  • Process Optimization: Drive process improvement initiatives to enhance consistency in aggregate reporting, signal management, clinical trial safety oversight, and ad hoc safety responses.
  • Implementation: Maintain existing procedures and support the rollout of new PV processes.

Essential Skills and Qualifications:
  • Data Interpretation & Communication: Ability to understand, interpret, analyze, and clearly present scientific and medical data verbally and in writing (including medical concepts and terminology).
  • Cross-Functional Collaboration: Proven track record of working collaboratively in a team environment across Safety, Clinical Development, Medical Affairs, Clinical Operations, Regulatory, and external colleagues.
  • Clinical Judgment: Ability to apply clinical judgment to interpret case information and guide staff on case data evaluation.
  • Regulatory & PV Knowledge: Familiarity with pharmacovigilance, drug development, clinical trial safety regulations, and post-marketing safety regulations (including case processing, expedited reporting, and safety databases).
  • Organization & Independence: Strong organizational skills with the ability to prioritize tasks independently with minimal supervision.
  • Technical Proficiency: Basic knowledge of standard software (Excel, PowerPoint, Word, Business Objects) and familiarity with common safety database systems.

Education & Experience Requirements:
  • Education: Bachelor’s degree in biological or natural sciences required; Advanced degree (MSc, PhD, MPH, PharmD, etc.) preferred.
  • Experience: Minimum of 5 years of Pharmacovigilance experience, including direct experience in aggregate safety report writing and safety signal management.

About Us:
Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.
IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.
Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.

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