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Remote Drug Safety Associate Jobs (NOW HIRING)

Spectra force

Medical Safety Physician

Lincolnton, NC · On-site +1

Company Description Medical Safety Physician 6-month assignment 100% Remote What are the three most ... adverse drug reactions, review medical inputs for into signal management and benefit-risk ...

Viridian Therapeutics, Inc.

Safety Scientist

Waltham, MA · On-site +1

$127K - $155K/yr

For a remote role, travel to headquarters may be required at discretion of management ... Knowledge of MedDRA and WHO Drug Dictionary terminology and its application as well as experience ...

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How much do remote drug safety associate jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for remote drug safety associate in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What does a typical workday look like for a Remote Drug Safety Associate?

A typical workday for a Remote Drug Safety Associate involves reviewing and processing adverse event reports, entering data into safety databases, and preparing regulatory submissions. You may also participate in teleconferences with cross-functional global teams, respond to queries from regulatory bodies, and support ongoing safety surveillance activities. The role generally requires self-motivation and strong organizational skills to manage tasks independently while collaborating virtually with colleagues in pharmacovigilance, clinical, and regulatory departments. Flexible work schedules and regular online meetings are common, making time management essential in a remote setting.

What are the key skills and qualifications needed to thrive in the Remote Drug Safety Associate position, and why are they important?

To thrive as a Remote Drug Safety Associate, you need a background in life sciences, pharmacovigilance, and regulatory compliance, often supported by a relevant degree (such as pharmacy, nursing, or a related field). Familiarity with safety databases like Argus or ARISg, as well as certifications such as Drug Safety Certified Professional (DSCP), is common in this role. Strong attention to detail, clear written communication, and the ability to work independently are key soft skills. These competencies help ensure drug safety information is managed accurately and efficiently in a remote environment, contributing to patient safety and regulatory compliance.

What is a Remote Drug Safety Associate job?

A Remote Drug Safety Associate is responsible for monitoring, assessing, and reporting adverse drug reactions (ADRs) to ensure medication safety and regulatory compliance. They review patient safety data, prepare safety reports, and liaise with healthcare professionals and regulatory agencies. Working remotely, they use specialized databases and communication tools to track and analyze drug safety information. Their role is crucial in ensuring that pharmaceuticals remain safe for consumers while complying with industry regulations.

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Remote Drug Safety Associate jobs near you
Infographic showing various Remote Drug Safety Associate job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, 11% Part Time, and 6% Contract. Highlights an 100% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.
Vice President Drug Safety

Vice President Drug Safety

Catalyst Pharmaceuticals, Inc.

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago

Job description

The Vice President (VP) of Drug Safety will lead drug safety operations across Catalyst's development and commercial portfolio, overseeing PV infrastructure, case management systems, vendor oversight, budget, compliance, training, and inspection readiness. Reporting to the Chief Medical Officer, this role provides strategic and operational leadership for the design and execution of drug safety capabilities and product/program specific drug safety plans in alignment with regulations and corporate goals.
This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical Development, Regulatory Affairs, Medical Affairs, Quality, Legal, and Commercial to enable efficient and compliant safety oversight across all programs. The VP, Drug Safety is also responsible for regular periodic regulatory updates and reports, along with spontaneous reporting as necessary and indicated.
This is a remote position that will require travel to company headquarters and other locations as needed to support business operations.
Requirements
Responsibilities (including but not limited to):
  • Develop and execute a strategic vision for the drug safety function, aligning with Catalyst's corporate goals and industry best practices
  • Lead PV operations, including collection, evaluation, and analysis of safety data from clinical trials, post-marketing sources, investigator-initiated studies, and real-world evidence
  • Oversee the preparation, quality control, and timely submission of expedited and periodic safety reports (e.g., ICSRs, DSURs, PSURs/PBRERs) to health authorities
  • Lead benefit-risk assessments and signal detection activities across the lifecycle of products, ensuring proactive identification and communication of emerging safety risks
  • Design and implement risk management strategies, including Risk Evaluation and Mitigation Strategies (REMS), to ensure patient safety and regulatory compliance
  • Provide PV subject matter expertise during Health Authority interactions, including inspections, audits, regulatory responses, and scientific advice meetings
  • Oversee the development, maintenance, and compliance of PV SOPs, work instructions, and training programs to ensure adherence to regulatory requirements
  • Drive inspection readiness efforts in collaboration with Quality and Regulatory teams, ensuring timely, thorough, and compliant responses to regulatory inquiries
  • Manage a high-performing team of PV professionals, fostering a culture of excellence, collaboration, and continuous improvement
  • Provide executive oversight of safety database infrastructure, MedDRA updates, and system enhancements in partnership with IT and external vendors
  • Ensure optimal execution of PV vendor partnerships, establishing service-level agreements, KPIs, and governance frameworks to ensure quality and accountability
  • Collaborate cross-functionally with Clinical Development, Regulatory, Medical Affairs, and Commercial to align safety strategy with product development and lifecycle plans
  • Contribute to scientific communication efforts, including publications, field training materials, and stakeholder engagement related to safety profiles
  • Participate in due diligence, alliance management, and external collaborations as needed, serving as the executive PV representative
  • Additional responsibilities include executive oversight of implementation of safety technologies, contribution to benefit-risk management, and representation on external alliances

Education/Experience/Skills:
  • MD in relevant clinical/scientific field
  • Minimum 15 years of pharmacovigilance experience in the biopharmaceutical industry, including at least 10 years in a senior leadership or management role overseeing Drug Safety functions
  • Broad therapeutic experience with Rare Diseases and/or neuromuscular disease experience being additive
  • Demonstrated experience leading safety operations across clinical development and post-marketing, with a strong understanding of the end-to-end safety lifecycle
  • Proven success in managing safety surveillance, signal detection, regulatory reporting, and compliance with regulatory requirements, including FDA, EMA, ICH, and GCP
  • Deep knowledge of Good Clinical Practice (GCP) and pharmacovigilance regulations and expectations, including adverse event reporting for investigational and marketed products
  • Experience with safety databases (e.g. ARGUS) and other pharmacovigilance systems and tools
  • Strong clinical judgment with the ability to assess complex safety data and provide clear, evidence-based recommendations
  • Excellent organizational and interpersonal skills, with a high degree of leadership credibility, initiative, and the ability to mentor high-performing teams
  • Ability to operate effectively in a fast-paced, biotechnology environment, adapting to dynamic priorities and cross-functional demands
  • Willingness to travel to company headquarters and other locations as needed to support business operations

Catalyst is committed to providing competitive wages and comprehensive benefits including health, dental, and vision insurance, generous paid time off, a retirement savings plan with Company Match, and more. Further details about our benefits package can be found here: https://www.linkedin.com/company/catalystforrare/life/life-at-catalyst/?viewAsMember=true
The base salary for this position will range from $405,000 to $430,000. Candidate experience, professional licensing, and geographic location will be taken into consideration.
Employment is contingent upon successful completion of all required screening and verification processes, including for authority to work in the United States.
EEO Statement
Catalyst Pharmaceuticals is an Equal Opportunity Employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status.
Recruitment & Staffing Agencies: Catalyst Pharmaceuticals does not accept unsolicited agency resumes. Agency resumes will only be accepted if the agency is formally engaged by Catalyst Human Resources.

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