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Safety Assistant Jobs in Reston, VA (NOW HIRING)

Overview Sr. Safety Monitor I Be Part of One Team, One Purpose. At Emmes Group , we're shaping the future of clinical research- where human intelligence meets cutting-edge technology to drive ...

Overview Sr. Safety Monitor I Be Part of One Team, One Purpose. At Emmes Group , we're shaping the future of clinical research- where human intelligence meets cutting-edge technology to drive ...

Assistant Superintendent

Mclean, VA · On-site

$75 - $100/hr

And we perform with MORE Pride--in focusing on safety and quality, and in offering more ... This is an assistant managerial position and reports to the Superintendent in charge of the project ...

And we perform with MORE Pride-in focusing on safety and quality, and in offering more ... This is an assistant managerial position and reports to the Superintendent in charge of the project ...

And we perform with MORE Pride--in focusing on safety and quality, and in offering more ... This is an assistant managerial position and reports to the Superintendent in charge of the project ...

And we perform with MORE Pride-in focusing on safety and quality, and in offering more ... This is an assistant managerial position and reports to the Superintendent in charge of the project ...

And we perform with MORE Pride-in focusing on safety and quality, and in offering more ... This is an assistant managerial position and reports to the Superintendent in charge of the project ...

Assistant Safety Manager The Assistant Safety Manager is responsible for the regular safety inspection of assigned HITT projects. This individual supports the Project Teams in the managing of safety ...

Be Seen First

Your leadership will drive team performance, uphold food safety standards, and maintain a welcoming ... Previous assistant manager or managerial experience within the food industry is preferred

Be Seen First

Your leadership will drive team performance, uphold food safety standards, and maintain a welcoming ... Previous assistant manager or managerial experience within the food industry is preferred

Showing results 21-40

Safety Assistant information

See Reston, VA salary details

$28.7K

$50.8K

$83.4K

How much do safety assistant jobs pay per year?

As of Sep 5, 2026, the average yearly pay for safety assistant in Reston, VA is $50,849.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,700.00 and $54,200.00 per year, depending on experience, location, and employer.

What is a safety assistant?

Safety Assistants are professionals who support the implementation of health and safety policies in workplaces. They help identify potential hazards, conduct routine safety inspections, and ensure compliance with safety regulations. Their duties often include assisting with safety training, maintaining records, and responding to incidents or emergencies. Safety Assistants work under the supervision of safety managers or officers to help create a safer work environment for everyone.

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

To thrive as a Safety Assistant, you need a solid understanding of workplace safety regulations, hazard identification, and incident reporting, often supported by a high school diploma or relevant safety certification. Familiarity with safety management systems, inspection checklists, and software like MS Office or safety database platforms is typically required. Strong attention to detail, communication skills, and the ability to work collaboratively help you stand out in this role. These competencies are vital for maintaining a safe work environment, preventing accidents, and ensuring compliance with safety standards.

What are some common challenges safety assistants face when ensuring compliance with safety protocols on-site?

Safety Assistants often encounter challenges such as ensuring all employees consistently follow safety protocols, especially in dynamic or fast-paced environments where procedures may be overlooked. They must also effectively communicate safety updates and address language or cultural barriers within diverse teams. Additionally, balancing administrative tasks like documentation with on-site inspections can be demanding. Proactive problem-solving and strong interpersonal skills are essential to successfully overcoming these challenges and maintaining a safe workplace.

What is the difference between Safety Assistant vs Safety Coordinator?

AspectSafety AssistantSafety Coordinator
CertificationsOSHA 10/30-hour, Basic Safety CertificationsOSHA 30-hour, Safety Management Certifications
Work EnvironmentConstruction sites, manufacturing plants, warehousesConstruction sites, industrial facilities, corporate safety programs
Employer & Industry UsageEntry-level safety support roles in various industriesSupervisory roles overseeing safety programs and compliance

Safety Assistants typically perform support tasks such as safety inspections and documentation, often requiring basic safety certifications. Safety Coordinators have more responsibility, including developing safety procedures and managing safety compliance. While both roles work in similar environments, Safety Coordinators usually have more experience and certifications, focusing on safety program management.

What are the most commonly searched types of Safety jobs in Reston, VA?

The most popular types of Safety jobs in Reston, VA are:

What job categories do people searching Safety Assistant jobs in Reston, VA look for?

The top searched job categories for Safety Assistant jobs in Reston, VA are:

What cities near Reston, VA are hiring for Safety Assistant jobs?

Cities near Reston, VA with the most Safety Assistant job openings:

Infographic showing various Safety Assistant job openings in Reston, VA as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $50,849 per year, or $24.4 per hour.

Sr. Safety Monitor I

Emmes Group

Rockville, MD • On-site

Full-time

Medical, Retirement

Posted 11 days ago


Job description

Overview
Sr. Safety Monitor I
Be Part of One Team, One Purpose.
At Emmes Group, we're shaping the future of clinical research-where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we've led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.
Through our two business units-Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions -we are modernizing clinical trials and accelerating the development of life-changing therapies.
We believe that every clinical breakthrough starts with people-people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.
The Senior Safety Monitor I will implement Pharmacovigilance activities in collaboration with other members of the Pharmacovigilance and Medical Monitoring (PMM) department under limited supervision. The Senior Safety Monitor I will be responsible for safety monitoring for interventional and non-interventional clinical projects in conjunction with the assigned Medical Monitor/Medical Officer and the project team. In addition, the Senior Safety Monitor I will supervise the design and execution of the assigned Pharmacovigilance (PV) related projects (e.g., management of local or international PV systems for contracted Clients; PV supervision of RWE (Real World Evidence projects); etc.) in close cooperation with other Emmes roles, especially with Medical Officers/ Medical Monitors (or other similar medical expert roles), Regulatory roles, etc. The Senior Safety Monitor I will support the adherence to Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP) and other relevant Pharmacovigilance requirements.
Responsibilities
  • Performs safety monitoring activities in cooperation with project Medical Monitor/Medical Officer and other relevant project team members.
    ° Reviews safety events.
    • Oversees the collection, assessment, monitoring, review and reporting of adverse drug reaction cases from all sources - clinical (both interventional and non-interventional), data sets analyzed in association with RWE projects, spontaneous reports, literature, etc.
    • Provides first line evaluation of serious adverse events (SAEs).
    • Communicates with site staff regarding reported AEs or SAEs to gather additional information.
    • Prepares a summary narrative for each reported SAE suitable for Medical Monitor/Officer review, and inclusion in Data Safety Monitoring Board (DSMB) reports, regulatory submissions, and final study reports.
    • Coordinates the timely completion and submission of required reports to necessary health authorities and business partners.
    • Maintains ongoing database of SAEs and reconciles SAEs in the database as needed.
    • Reviews adverse events and/or other safety related data such as toxicities, concomitant medications and medical history, etc. for the study on a regular basis.
    ° Establishes direct communication with Client, investigator site staff, national and regional regulatory authorities, health professionals, pharmaceutical and other study partners, as necessary.
    • Responds to site, Client, DSMB, or Medical Monitor/Officer requests for information regarding safety in clinical trials (both interventional and non-interventional).
    • Participates in DSMB or other safety review committee (SRC) meetings, including Protocol Safety Review Team (PSRT) meetings, as necessary.
    • Reviews and contributes to DSMB/SRC reports regarding safety; reviews and contributes to safety sections of annual report as well as periodic safety reports.
    ° Coordinates with project staff.
    • Participates in project team meetings for the planning, preparation, and development of all safety-related sections of protocols, study specific safety documents such as Safety Management Plan (SaMP), Manual of Operations (MOP), project Standard Operating Procedures (SOPs), and ancillary documents to ensure project compliance with corporate SOPs.
    • Contributes to the development and implementation of the safety related Case Report Forms (CRF) and SaMP.
    • Ensures maintenance of documentation required by both corporate and project SOPs.
    • Participates in project process improvement and corporate quality assurance activities through Internal Quality Audit Team (IQAT) processes, project SOPs and Compliance/Variance table development, participation in both internal and external audits, as well as professional development activities.
    ° Performs Medical Dictionary for Regulatory Activities (MedDRA) and World Health Organization (WHO) Drug coding, as applicable.
  • Guarantees compliance and adherence to the quality standards.
    • Contributes to the development and maintenance of departmental quality documents (e.g., SOPs) and other work practices as assigned.
    • Maintains accurate reporting to relevant authorities, such as Food and Drug Administration (FDA), European Medicines Agency (EMA) etc. when applicable per client contract. Contributes to the verification that Quality Control processes are conducted in accordance with applicable written procedures.
    • Completes all relevant professional training in the given scope and time frame.
  • Acts as a mentor/resource for junior colleagues.
  • Drives other corporate activities including development and presentation of Emmes internal training courses, chairing of corporate safety meetings/activities, coordination of annual SOP reviews, coordination of cross-department working groups dedicated to improvement of work processes and development of innovative solutions and other relevant corporate activities.

Qualifications
  • Bachelor's Degree in pharmacology, nursing or other scientific discipline is required with relevant experience in clinical practice (e.g., pharmacy, inpatient or outpatient healthcare facility, clinical research center, etc.)
  • 4-6 years related experience in research or with a pharmaceutical company (CRO, pharma company, etc.) with prior experience in safety monitoring/pharmacovigilance Required
  • 1-3 years of experience in safety monitoring/pharmacovigilance with some mentoring of junior staff preferred
  • Working knowledge of MedDRA and WHO Drug coding preferred.
  • Demonstrated use of medical terminology and ability to extract information to create a case history.
  • Consistency, quality, compliance and patient centricity respected as key values.
  • Excellent clinical judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way.
  • Excellent oral and written communication skills.
  • Ability to work as a team member and function on a cross-functional team.
  • Capacity to provide leadership and creativity in the work environment.
  • Detail oriented with good organizations skills.
  • Ability to complete work autonomously.

If you're looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.
Why work at Emmes?
At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:
  • Flexible Approved Time Off

  • Tuition Reimbursement

  • 401k Retirement Plan
  • Work From Home Anywhere in the US

  • Maternal/Paternal Leave

  • Casual Dress Code & Work Environment

CONNECT WITH US!
Follow us on Twitter - @EmmesCRO
Find us on LinkedIn - Emmes
The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.
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