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Remote Drug Safety Associate Jobs (NOW HIRING)

About the Role The Medical Safety (MS) Specialist is responsible for providing medical expertise and assessment to support patient safety throughout the lifecycle as both an advocate for patient ...

... drug safety, health economics and outcomes research, regulatory affairs, quality assurance ... The position is a 3 month, 40 hour a week REMOTE engagement. The therapeutic areas include ...

Works cross-functionally to plan and verify safety database configuration compliance based on PV ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

... drug safety (global experience is a plus) * Proven leadership, motivational and interpersonal ... LI-Remote For applicants in the United States: The annual base salary hiring range for this ...

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Remote Drug Safety Associate information

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$12

$49

$85

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

As of Jul 5, 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.

More about Remote Drug Safety Associate jobs
What cities are hiring for Remote Drug Safety Associate jobs? Cities with the most Remote Drug Safety Associate job openings:
What are the most commonly searched types of Remote Drug Safety jobs? The most popular types of Remote Drug Safety jobs are:
What states have the most Remote Drug Safety Associate jobs? States with the most job openings for Remote Drug Safety Associate jobs include:
Infographic showing various Remote Drug Safety Associate job openings in the United States as of June 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 100% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Medical Safety Spec

MiniMed

Northridge, CA โ€ข On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago


Job description

We anticipate the application window for this opening will close on - 3 Jul 2026
At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world.
About the Role
The Medical Safety (MS) Specialist is responsible for providing medical expertise and assessment to support patient safety throughout the lifecycle as both an advocate for patient safety and in support of safe and effective use of Diabetes products and therapies.
With general supervision, the MS Specialist works on a range of medical safety activities of varying complexity in collaboration with MS team members and other functions, including Risk Management, Quality/ Post-Market Vigilance, Research & Development, Regulatory, and Clinical. The MS Specialist primarily interacts with MS personnel, with other functions as needed to share information or gain input to support decision making.
The MS Specialist will apply medical knowledge, clinical expertise, and product knowledge support to patient safety through the application of:
Medical Input:
  • Basic understanding of practical medical/scientific concepts.
  • General knowledge in medical specialties, diagnoses, treatments, and procedures related to product and therapy area.
  • Basic understanding of how to search medical/scientific databases and evaluate literature.
  • Leverage medical knowledge and advocate for patient safety by providing medical safety input to internal functions and business processes across the product life cycle where the Medical Safety role is defined.
  • May be involved in cross-functional assignments.

Medical Safety Assessments:
  • Evaluate events and potential safety signals identified through Quality, Clinical, and Regulatory related business unit processes.
  • Author high-quality and accurate safety assessments per business unit processes, leveraging complaint data, literature, registries, or other data sources as appropriate.
  • Critically assess and escalate newly identified safety issues (suspected increase in severity and/or frequency of known events or new events with a causal relationship to the device) per business unit processes for investigation assessment and action.
  • Assist with obtaining input from external medical and subject matter experts on safety matters.
  • Complete qualitative and quantitative assessments of post market adverse events, medical significance, and recommendations for inclusion in regulatory annual reports.

Safety Inquiries:
  • Provide evidence-based medical safety input, education and/or response to safety inquiries from internal or external stakeholders (e.g., external medical personnel or other third-parties, including regulatory agencies or health care organizations).

Product therapy and knowledge:
  • Basic understanding of supported therapy indications and relevant disease states.
  • Understands product design and use, basic mechanism of action, product labeling, and general safety profile.

Business Acumen:
  • Basic understanding of key medical device lifecycle processes.
  • Knowledge of governing regulations and key industry practices related to the function.
  • General awareness of organizational design, functional roles, and key business strategies.
  • Aware of and contributes to the Medical Safety Function strategy success.

Medical Communication and Influence:
  • Basic ability to interpret, synthesize, write, and present medical information in an accurate and logical manner.
  • Interacts primarily and effectively with internal peers. External interactions are less complex or problem solving in nature.
  • May provide guidance and assistance to entry level professionals and /or employees in the support career stream.
  • Adapt verbal and written communication style to situational context.
  • Adapt to changing priorities and work demands.

Must-Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident on your resume.
  • Licensed healthcare professional or certified personnel with clinical knowledge and relevant patient care experience (e.g., RN, RD, MD, PA, NP).
  • Bachelor's degree with a minimum of 2 years of Clinical Experience in Diabetes, Medical Safety/Medical Affairs, or an advanced degree with a minimum of 1 year of experience in Diabetes, Medical Safety/Medical Affairs.

Nice to Have
  • Basic ability to understand and apply practical medical and product knowledge in a competent manner for Medical Safety activities.
  • Able to make competent, risk-based, and timely medical safety decisions based on insightful analysis of critical information; able to balance analysis with decisiveness.
  • Able to understand scientific/technical concepts and function of medical devices.
  • Able to effectively communicate verbally and in writing, and effectively influence diverse stakeholders (team members, functional partners, and HCPs).
  • Solid medical background with the ability to understand complex disease states and different treatment outcomes and complications.
  • Versatile learner, able to quickly and effectively integrate new information and skills.
  • Solid critical thinking and problem-solving skills.
  • High attention to detail and accuracy; able to work independently with general supervision; accountable for outcomes.
  • Able to develop trusted relationships and collaborate with co-workers and key functional partners.
  • Excellent verbal and written communication skills.
  • CDCES, Certified Diabetes Care and Education Specialist.

Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
Benefits & Compensation
MiniMed offers a competitive salary and flexible benefits package
At MiniMed, we put people first. A commitment to our employees lives at the core of our values: We recognize their contributions. They share in the success they help create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every stage of your career and life.
Salary ranges for U.S (excl. PR) locations (USD):$68,000.00 - $116,000.00
Actual compensation may vary based on factors including experience, education, certifications, skills, market conditions, internal equity, and geographic location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
This position is eligible for a short-term incentive called the Short Term Incentive (STI).
At MiniMed, we are committed to supporting the well-being and financial security of our employees. Regular employees working 20 or more hours per week are eligible for a robust benefits package, including health, dental, and vision insurance, as well as access to a Health Savings Account, Healthcare Flexible Spending Account, life insurance, long-term disability leave, and a dependent daycare spending account. In addition, all regular employees enjoy incentive plans, a 401(k) plan with company match, short-term disability coverage, paid time off and holidays, participation in our Employee Stock Purchase Plan, and access to our Employee Assistance Program. Eligible employees may also benefit from our Non-qualified Retirement Plan Supplement and Capital Accumulation Plan, subject to IRS minimum earnings requirements. Please note that "regular employees" refers to those who are not temporary staff, such as interns, and some benefits may not apply to employees in Puerto Rico.
For further details about our comprehensive benefits, we encourage you to visit the link below.
MiniMed Benefits Overview
About MiniMed
MiniMed is a full-stack insulin delivery company dedicated to supporting people living with diabetes through every step of their journey - when and how they need it. For more than 40 years, we've been committed to redefining what's possible: intelligent dosing systems designed for real life, predictive insights that stay a step ahead, and always on support when it's needed most. At the heart of everything we do is a simple Mission: to make every day a better day for people with diabetes.
Learn more about our business, and our mission here.
It is the policy of MiniMed to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, familial status, membership or activity in a local human rights commission, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state, or local law. In addition, MiniMed will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for MiniMed in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which MiniMed reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. MiniMed will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.