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Siv Jobs in Virginia (NOW HIRING)

Alcanza Clinical Research

$23.50 - $31.25/hr

Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed; * Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team ...

Alcanza

Clinical Research Coordinator

Fredericksburg, VA

$23.75 - $31.75/hr

Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed; * Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team ...

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Siv information

See Virginia salary details

$5

$90

$190

How much do siv jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for siv in Virginia is $90.66, according to ZipRecruiter salary data. Most workers in this role earn between $51.49 and $190.67 per hour, depending on experience, location, and employer.

What is a siv?

Siv is not a widely recognized job title, and its meaning may vary depending on the industry or company. It could be an abbreviation or a specialized role within a specific field. If you have more context, such as the industry or organization, it would be easier to determine the exact responsibilities and qualifications for a Siv job.

What are some common challenges faced by civil engineers when working on large infrastructure projects?

Civil engineers often encounter challenges such as coordinating with multidisciplinary teams, managing tight project deadlines, and addressing unexpected site or regulatory issues. Effective communication with contractors, architects, and government agencies is crucial to ensure project goals are met. Additionally, adapting to changes in project scope or environmental conditions requires strong problem-solving skills and flexibility. Staying organized and proactive can help civil engineers navigate these challenges successfully.

What are the key skills and qualifications needed to thrive as a civil engineer, and why are they important?

To thrive as a Civil Engineer, you need a solid understanding of structural analysis, mathematics, and engineering principles, typically supported by a bachelor’s degree in civil engineering and professional licensure (PE). Familiarity with technical tools such as AutoCAD, Civil 3D, and project management software is highly valued. Strong problem-solving abilities, teamwork, and effective communication set top performers apart in this field. These competencies are essential for ensuring safe, efficient, and sustainable infrastructure projects that meet regulatory and client requirements.

What is the difference between Siv vs Data Analyst?

AspectSivData Analyst
Required CredentialsTypically requires certifications in security, networking, or specific Siv toolsUsually requires a degree in statistics, computer science, or related fields
Work EnvironmentPrimarily in security operations centers, IT departments, or cybersecurity firmsOften in business, finance, or tech companies analyzing data sets
Employer & Industry UsageUsed by cybersecurity teams, IT departments, and government agenciesEmployed across industries like finance, marketing, healthcare, and tech

While both Siv and Data Analysts work with technical data, Siv focuses on security and network monitoring, whereas Data Analysts analyze data to inform business decisions. Their credentials, work environments, and industry applications differ, making each role specialized in its domain.

What are popular job titles related to Siv jobs in Virginia?

For Siv jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Siv jobs in Virginia look for?

The top searched job categories for Siv jobs in Virginia are:

Siv jobs near you
Infographic showing various Siv job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $188,582 per year, or $90.7 per hour.

Clinical Research Coordinator

Alcanza Clinical Research

On-site

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 2 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in  MA, NH, MI, VA, SC, FL, GA and AL. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.  

Key Responsibilities
In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 
  • Screening of patients for study enrollment;
  • Patient consents;
  • Patient follow-up visits;
  • Documenting in source clinic charts;
  • Entering data in EDC and answers queries;
  • Obtaining vital signs and ECGs;
  • May perform basic lab procedures per protocol, such as:  blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; 
  • Requesting and tracking medical record requests;
  • Updating and maintaining logs, chart filings; 
  • Maintaining & ordering study specific supplies;
  • Scheduling subjects for study visits and conducts appointment reminders;
  • Building/updating source as needed;
  • Conducting monitoring visits and resolves issues as needed in a timely manner;
  • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
o    Filing SAE/Deviation reports to Sponsor and IRB as needed;
o    Documenting and reporting adverse events;
o    Reporting non-compliance to appropriate staff in timely manner;
o    Maintaining positive and effective communication with clients and team            
       members;
o    Always practicing ALCOAC principles with all documentation;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
  • Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
  • Assist with training of new research assistants and coordinators;
  • Assist with scheduling and planning for visit capacity for assigned studies;
  • May set up, train and maintain all technology needed for studies;
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • May handle more complex study assignments and volumes;
  • May participate in community outreach / education events;
  • Maintaining confidentiality of patients, customers and company information,       and;
  • Performing all other duties as requested or assigned.


Skills, Knowledge and Expertise
Minimum Qualifications:  A Medical Assistant diploma, LPN/LVN, EMT credential AND 1+ years of clinical research coordination experience, OR an equivalent combination of education and experience, is required.  Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.  CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.  

 Required Skills: 
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills. 
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines. 

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.