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Full Time Edc Security Jobs (NOW HIRING)

Clinical Research Coordinator I

Maplewood, MN ยท On-site

$24.75 - $33/hr

Headlands Research - Twin Cities| [[Full-Time]] | Clinical Research Are you an experienced clinical ... Ensure timely data entry and resolution of EDC queries * Report and follow up on all adverse events ...

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Full Time Edc Security information

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How much do full time edc security jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for full time edc security in the United States is $25.98, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $29.33 per hour, depending on experience, location, and employer.

What is the difference between Full Time Edc Security vs Full Time Security Guard?

AspectFull Time Edc SecurityFull Time Security Guard
CredentialsSecurity certification, sometimes specialized in electronic securityBasic security training, security guard license
Work EnvironmentElectronic security systems, access control, alarm monitoringPhysical patrols, access points, on-site presence
Employer & IndustrySecurity companies, corporate facilities, electronic security providersCommercial buildings, retail, industrial sites

Full Time Edc Security focuses on electronic security systems and monitoring, requiring specialized certifications, while Full Time Security Guard involves physical patrols and on-site security, often with basic training. Both roles are essential in the security industry but differ in their daily tasks and skill requirements.

What are some common challenges faced by Full Time EDC Security personnel, and how are they addressed on the job?

Full Time EDC Security personnel often face challenges such as maintaining constant vigilance in fast-paced environments, effectively responding to security incidents, and adapting to evolving safety protocols. To address these challenges, ongoing training is provided, strong teamwork and communication are emphasized, and clear procedures are established for handling emergencies. Collaboration with other departments and regular briefings help ensure everyone is prepared to manage risks and maintain a safe environment.

What are Full Time EDC Security jobs?

Full Time EDC Security jobs involve providing security services at Event and Exhibition Centers (EDC) on a full-time basis. These roles typically include monitoring premises, ensuring the safety of visitors and staff, responding to emergencies, and enforcing venue policies. Full-time EDC Security personnel may also assist with crowd control during events, check credentials, and report any suspicious activities. The job requires excellent communication skills, attention to detail, and the ability to handle stressful situations effectively.

What are the key skills and qualifications needed to thrive as a Full Time EDC Security Officer, and why are they important?

To thrive as a Full Time EDC Security Officer, you need a solid understanding of security protocols, surveillance techniques, and often a high school diploma or equivalent. Familiarity with security systems such as CCTV, access control systems, and sometimes certifications like CPR, first aid, or a security guard license are typically required. Strong observational skills, professionalism, and effective communication help you respond calmly and efficiently to incidents. These skills ensure safety, prevent incidents, and maintain a secure environment at large-scale events or facilities.
More about Full Time Edc Security jobs
What cities are hiring for Full Time Edc Security jobs? Cities with the most Full Time Edc Security job openings:
What are the most commonly searched types of Edc Security jobs? The most popular types of Edc Security jobs are:
What states have the most Full Time Edc Security jobs? States with the most job openings for Full Time Edc Security jobs include:
What job categories do people searching Full Time Edc Security jobs look for? The top searched job categories for Full Time Edc Security jobs are:
Infographic showing various Full Time Edc Security job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 84% In-person, 11% Hybrid, and 5% Remote job distribution, with an average salary of $54,037 per year, or $26 per hour.

Clinical Research Coordinator I

Headlands Research

Maplewood, MN โ€ข On-site

$24.75 - $33/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago


Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Clinical Research Coordinator (CRC)
Location: Maplewood, MN | Site Name: Headlands Research - Twin Cities| [[Full-Time]] | Clinical Research
Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Maplewood, MN. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.
Type: Regular Full-time Employee
Schedule: Mondays through Fridays, 8:00am - 4:30pm
Location: Onsite in Maplewood, MN (no capabilities for remote or hybrid work)
Reports to: Site Director
Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.
What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us?
You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.
Responsibilities:
  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements:
  • Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP
  • Previous experience as a Clinical Research Coordinator
  • Industry-sponsored trial experience strongly preferred (vaccine study experience a plus)
  • Familiarity with electronic data capture (EDC), IVRS, and other trial platforms
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.