Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies. * Writes procedural documents including Standard ...
Quick apply
Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies. * Writes procedural documents including Standard ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and operational leadership for safety science activities across the company's clinical development and ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and operational leadership for safety science activities across the company's clinical development and ...
Associate Director Global Patient Safety
Warren, MI · On-site
$157K - $256K/yr
We are seeking an Associate Director, PV Case Operations to join our Global Patient Safety team ... Typically 10 years of Pharmacovigilance, Drug Safety, or PV Quality experience in pharma or biotech.
Associate Director Global Patient Safety
Warren, MI · On-site
$157K - $256K/yr
We are seeking an Associate Director, PV Case Operations to join our Global Patient Safety team ... Typically 10 years of Pharmacovigilance, Drug Safety, or PV Quality experience in pharma or biotech.
Environmental Health & Safety Associate Triumvirate Environmental, one of the largest environmental ... Upon employment, you will be required to participate in a random drug screening program (inclusive ...
Environmental Health & Safety Associate Triumvirate Environmental, one of the largest environmental ... Upon employment, you will be required to participate in a random drug screening program (inclusive ...
Pharmacovigilance Expert
Ann Arbor, MI · 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 ...
Pharmacovigilance Expert
Ann Arbor, MI · 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 ...
Pharmacovigilance Expert
Lansing, MI · 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 ...
Pharmacovigilance Expert
Lansing, MI · 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 ...
Pharmacovigilance Expert
Grand Rapids, MI · 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 ...
Pharmacovigilance Expert
Grand Rapids, MI · 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 ...
The successful candidate may be required to complete a background check and a drug test as a ... safety. Thanks to us our assets, co-workers, visitors and customers can feel safe. At least we ...
The successful candidate may be required to complete a background check and a drug test as a ... safety. Thanks to us our assets, co-workers, visitors and customers can feel safe. At least we ...
Pharmacovigilance Expert
Detroit, MI · 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 ...
Pharmacovigilance Expert
Detroit, MI · 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 ...
Pharmacovigilance Expert
Sterling Heights, MI · 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 ...
Pharmacovigilance Expert
Sterling Heights, MI · 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 ...
Pharmacovigilance Expert
Warren, MI · 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 ...
Pharmacovigilance Expert
Warren, MI · 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 ...
Pharmacovigilance Expert
Dearborn, MI · 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 ...
Pharmacovigilance Expert
Dearborn, MI · 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 ...
... drug applications and other regulatory filings * Assist GSO in developing a strategy for safety ... Associate's degree and 10 years of related experience OR High school diploma / GED and 12 years of ...
... drug applications and other regulatory filings * Assist GSO in developing a strategy for safety ... Associate's degree and 10 years of related experience OR High school diploma / GED and 12 years of ...
As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy ... drug safety and efficacy. * In collaboration with IVD Regulatory, support global regulatory ...
As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy ... drug safety and efficacy. * In collaboration with IVD Regulatory, support global regulatory ...
Safety Advisor
Ann Arbor, MI · On-site
The Associate in this role will be working in a Construction setting. 40-50 hours per week. This ... Site safety observations, including documentation of findings * Oversee all construction ...
Safety Advisor
Ann Arbor, MI · On-site
The Associate in this role will be working in a Construction setting. 40-50 hours per week. This ... Site safety observations, including documentation of findings * Oversee all construction ...
Safety Advisor
Ann Arbor, MI · On-site
The Associate in this role will be working in a Construction setting. 40-50 hours per week. This ... Site safety observations, including documentation of findings * Oversee all construction ...
Safety Advisor
Ann Arbor, MI · On-site
The Associate in this role will be working in a Construction setting. 40-50 hours per week. This ... Site safety observations, including documentation of findings * Oversee all construction ...
Safety Advisor
Ann Arbor, MI · On-site
Safety Management Group is a nationally recognized professional service organization that provides ... The Associate in this role will be working in a Construction setting. 40-50 hours per week. This ...
Safety Advisor
Ann Arbor, MI · On-site
Safety Management Group is a nationally recognized professional service organization that provides ... The Associate in this role will be working in a Construction setting. 40-50 hours per week. This ...
Safety Engineer
Canton, MI · On-site
Pilz Automation Safety L.P. is technology leader in safe automation technology. In this area, Pilz is consistently developing a role as a total solutions supplier with solutions for safety and ...
Quick apply
Safety Engineer
Canton, MI · On-site
Pilz Automation Safety L.P. is technology leader in safe automation technology. In this area, Pilz is consistently developing a role as a total solutions supplier with solutions for safety and ...
Safety Manger
Dearborn, MI · On-site
Description We at MAC Safety seek out the best and brightest safety professionals in the country. With our current clientele, we can place safety professionals in fast-paced diverse environments ...
Safety Manger
Dearborn, MI · On-site
Description We at MAC Safety seek out the best and brightest safety professionals in the country. With our current clientele, we can place safety professionals in fast-paced diverse environments ...
Safety Engineer
Canton, MI · On-site
Pilz Automation Safety L.P. is technology leader in safe automation technology. In this area, Pilz is consistently developing a role as a total solutions supplier with solutions for safety and ...
Quick apply
Safety Engineer
Canton, MI · On-site
Pilz Automation Safety L.P. is technology leader in safe automation technology. In this area, Pilz is consistently developing a role as a total solutions supplier with solutions for safety and ...
Drug Safety Associate information
See Michigan salary details
$10.69 - $16.51
7% of jobs
$16.51 - $22.34
4% of jobs
$22.34 - $28.17
3% of jobs
$33.34 is the 25th percentile. Wages below this are outliers.
$28.17 - $34
12% of jobs
The median wage is $38.52 / hr.
$34 - $39.83
31% of jobs
$39.83 - $45.66
15% of jobs
$47.38 is the 75th percentile. Wages above this are outliers.
$45.66 - $51.48
12% of jobs
$51.48 - $57.31
0% of jobs
$57.31 - $63.14
9% of jobs
$63.14 - $68.97
5% of jobs
$68.97 - $74.80
2% of jobs
$10
$42
$74
How much do drug safety associate jobs pay per hour?
As of Aug 10, 2026, the average hourly pay for drug safety associate in Michigan is $42.83, according to ZipRecruiter salary data. Most workers in this role earn between $33.51 and $48.41 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?
| Aspect | Drug Safety Associate | Pharmacovigilance Specialist |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or healthcare, with certifications like PV or drug safety training | Similar credentials, often with additional certifications or experience in pharmacovigilance |
| Work Environment | Pharmaceutical companies, CROs, or healthcare settings focusing on safety data management | Same as Drug Safety Associate, often with more specialized pharmacovigilance tasks |
| Employer & Industry | Pharmaceutical, biotech, and healthcare industries | Same 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.
More about Drug Safety Associate jobs
What are the most commonly searched types of Drug Safety jobs in Michigan? The most popular types of Drug Safety jobs in Michigan are:
What are popular job titles related to Drug Safety Associate jobs in Michigan? For Drug Safety Associate jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Drug Safety Associate jobs in Michigan look for? The top searched job categories for Drug Safety Associate jobs in Michigan are:
What cities in Michigan are hiring for Drug Safety Associate jobs? Cities in Michigan with the most Drug Safety Associate job openings:
What are popular job titles related to Drug Safety Associate jobs in MI? For Drug Safety Associate jobs in MI, the most frequently searched job titles are:
Full-time
Posted 26 days ago
Job description
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Senior Pharmacovigilance System Architect
We are recruiting for an experienced Pharmacovigilance System Architect (Argus Administrator SME) to join our US team.
Roles & Responsibilities
- Serves as Database Administrator for Argus Safety, including database configuration, issue resolution, maintenance, governance and daily support.
- Performs installations, upgrades, configuration of reporting rules, and E2B reporting via gateway technologies (including set-up and configuration of Axway Gateway Interchange).
- Provides support for all systems associated with PV and drug safety.
- Performs updates to Argus configuration and processes as per changing EudraVigilance regulations.
- Provides support and execution of activities related to EudraVigilance testing for various clients.
- Performs case migration/database transfers, file importing and supports other case processing activities.
- Provides leadership in executing Argus upgrades and related activities.
- Provides administrator support for other safety databases (such as ARISg).
- Performs periodic coding dictionary (MedDRA & WHO drug) updates for Argus.
- Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies.
- Writes procedural documents including Standard Operating Procedures (SOP), Work Practice Documents, and Data Entry Manuals for Argus Safety.
- Generates case processing metrics, reviews and makes suggestions and supports process improvement implementation.
- Maintains technical expertise of regulatory requirements and ensures alignment with company working practices.
- Assists with business development and capabilities efforts as needed.
- Interacts directly and independently with client to coordinate all facets of projects; competent communicator, supports client capabilities as PV/drug safety systems SME.
- Strong understanding and experience working with Argus configuration and study set up.
- Strong understanding of global case processing and SAE reporting.
- Strong understanding of global clinical trial development and data.
Requirements
- College graduate Information Technology discipline or related field, or relevant experience.
- Minimum of 5 years’ experience in Information Technology or similar field required.
- Expert knowledge of scientific principles and concepts.
- Reputation as emerging leader in field with sustained performance and accomplishment.
- Proficiency with MS Office applications.
- Hands-on experience with clinical trial and pharmaceutical development preferred.
- Good communication skills and willingness to work with others to clearly understand needs and solve problems.
- Excellent problem-solving skills.
- Good organizational and communication skills.
- Familiarity with current ISO 9001 and ISO 27001 standards preferred.
- Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
- Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
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About M. M. S.
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1 - 10 Employees
Headquarters location
Los Angeles, CA, US
Year founded
1980