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Protocol Associate Jobs in Illinois (NOW HIRING)

Warehouse Associate

Woodridge, IL ยท On-site

$19 - $20/hr

Warehouse Associate City : Woodridge, IL Job Summary We are seeking a dedicated and detail-oriented ... Follow safety protocols and guidelines while performing all tasks within the warehouse. Experience

Production Associate

Batavia, IL ยท On-site

$16 - $18/hr

All associates are expected to meet efficiency standards, maintain a clean and safe work environment and adhere to all safety protocols. Adhering to our attendance policy is a key element for success ...

Production Associate

Batavia, IL ยท On-site

$16 - $18/hr

All associates are expected to meet efficiency standards, maintain a clean and safe work environment and adhere to all safety protocols. Adhering to our attendance policy is a key element for success ...

Part Time Sales Associate

Belvidere, IL ยท On-site

$16 - $18/hr

Benefitting You As A Sales Associate: * Flexible Scheduling - You undoubtedly have commitments to ... Be ready to work in accordance with all Club Car Wash rules, policies, and protocols * Display a ...

Service Associate

Peoria, IL

$15.50 - $20.50/hr

Our Service Associate reports directly to the Operations Manager and is responsible for providing ... Follow safety protocols and procedures to ensure the well-being of all gym members and staff.

Benefitting You As A Sales Associate: * Flexible Scheduling - You undoubtedly have commitments to ... Be ready to work in accordance with all Club Car Wash rules, policies, and protocols * Display a ...

Benefitting You As A Sales Associate: * Flexible Scheduling - You undoubtedly have commitments to ... Be ready to work in accordance with all Club Car Wash rules, policies, and protocols * Display a ...

Benefitting You As A Sales Associate: * Flexible Scheduling - You undoubtedly have commitments to ... Be ready to work in accordance with all Club Car Wash rules, policies, and protocols * Display a ...

Part Time Sales Associate

Sterling, IL ยท On-site

$16 - $18/hr

Benefitting You As A Sales Associate: * Flexible Scheduling - You undoubtedly have commitments to ... Be ready to work in accordance with all Club Car Wash rules, policies, and protocols * Display a ...

Production Associate

Manteno, IL ยท On-site

$20/hr

We are seeking a skilled and motivated Production Associate to join our team at Gotion ... Adhere to safety protocols, including proper handling of materials and waste disposal. * Follow ...

Showing results 41-60

Protocol Associate information

What is the difference between Protocol Associate vs Clinical Research Coordinator?

AspectProtocol AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, often in life sciences or related fieldBachelor's degree, often in health sciences or related field
Work EnvironmentResearch institutions, pharmaceutical companies, clinical trial sitesHospitals, clinics, research centers
Employer & Industry UsageUsed in clinical research and pharmaceutical industriesCommon in clinical trial management and healthcare settings
Common Search & Comparison IntentYesYes

The main difference between a Protocol Associate and a Clinical Research Coordinator lies in their specific roles within clinical trials. Protocol Associates primarily focus on managing trial documentation, ensuring protocol compliance, and supporting regulatory submissions. Clinical Research Coordinators are more involved in patient recruitment, data collection, and day-to-day trial operations. Both roles require similar educational backgrounds and work in related environments, but their responsibilities differ based on the trial phase and organizational structure.

How does a Protocol Associate typically contribute to organizing high-profile events or meetings?

Protocol Associates play a vital role in ensuring that high-profile events and meetings run smoothly by managing logistics, adhering to diplomatic protocols, and coordinating with various stakeholders. They often handle guest lists, seating arrangements, and the flow of official communications, ensuring all cultural and organizational standards are met. Collaboration with event planners, security teams, and senior officials is common, making strong organizational and interpersonal skills essential. This role provides exposure to international relations and offers significant opportunities for growth in diplomatic or governmental settings.

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

To thrive as a Protocol Associate, you need strong organizational abilities, attention to detail, and a background in international relations or event management, often supported by a relevant bachelor's degree. Familiarity with scheduling software, database management systems, and sometimes knowledge of diplomatic protocols or languages is valuable. Excellent interpersonal skills, cultural sensitivity, and clear communication help build relationships and manage high-profile events smoothly. These competencies ensure that all protocol activities are executed flawlessly, maintaining professionalism and fostering positive diplomatic or organizational relations.

What are Protocol Associates?

Protocol Associates are professionals who assist in planning, organizing, and executing formal events, meetings, or ceremonies, often for government, diplomatic, or corporate organizations. They ensure that events adhere to proper procedures, etiquette, and established protocols. Their responsibilities may include managing guest lists, coordinating logistics, and advising on cultural customs to facilitate smooth interactions between parties. Protocol Associates play a key role in maintaining the organization's image and fostering positive relationships with stakeholders.
What are the most commonly searched types of Protocol jobs in Illinois? The most popular types of Protocol jobs in Illinois are:
What cities in Illinois are hiring for Protocol Associate jobs? Cities in Illinois with the most Protocol Associate job openings:
Research Associate Scientific II

Research Associate Scientific II

DivIHN Integration Inc

Round Lake, IL โ€ข On-site

Contractor

Posted yesterday


Job description

For further inquiries regarding the following opportunity, please contact our Talent Specialist
Prawin at 224 369 2969ย 
ย 
Title: Research Associate Scientific II
Location: Onsite/Hybrid in Round Lake, IL, 3 days onsite and 2 days remote
Duration: 18 Months contract
Work Schedule: 8-hour workdays (between 7-5)
ย 
Top 3-5 Must-Have Non-Negotiable Skills Required
1. Basic technical understanding of sterilization (Moist Heat, Aseptic, Irradiation)
2. Basic technical understanding of microbiological method validations (sterility, bioburden and bacterial endotoxin) (specific for the Research Associate II)
3. Ability to write, execute and review validation and qualification protocols and reports.
4. Ability to evaluate and interpret technical data and test results
Bachelorโ€™s degree required
ย 
These roles would be geared towards a Sterility Assurance support role will focuses on Microbiology.
2-4 years of recent experience preferred
ย 
Nice to Have Skills
1. Understanding of aseptic technique (RAII)
2. Ability to conduct experiments with minimal assistance
3. Knowledge and understanding of GxP and related regulations and guidance
ย 
ย 
  • Effectively contribute solid technical knowledge to a variety of projects within the sterility assurance discipline with minimal assistance.
  • Display basic technical understanding of related sterility assurance disciplines, specifically sterilization modalities and/or microbiological test method validation.
  • Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not. Provide some analysis/redesign of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility.
  • Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines.
  • Maintain knowledge of relevant Quality System Regulations and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
  • Recommend appropriate designs, techniques and processes for a specified sequence of tasks where needed.
  • In-depth knowledge and understanding of GxP and related regulations and guidance.
  • Provide support to the Sterility Assurance Focal Point for product development or on change controls.
  • Write, execute and review validation and qualification protocols and reports.
  • Evaluate and interpret technical data and test results.
  • The position requires relevant laboratory skills, writing skills, and computer skills plus teamwork/interpersonal skills.
  • Bachelor's Degree ย in a scientific discipline with at least 2-4 years lab experience.
  • Background in microbiology
  • somebody that knows the basics of microbiology, aseptic technique has worked with organisms in a lab.
  • Ideally would be somebody that has a sterile assurance.
  • Understanding a little bit of the micro methods and validations required for a pharmaceutical company.
  • it's a research associate 2 level, so has a few years of experience in the lab.
  • And also looking for them to help with report generation. So analyzing data and putting it into a template for report.
  • word, excel basic general understanding of the Microsoft platform would be enough.
  • work will be report generation and data analysis, probably 80% 20%.
  • Bachelors degree 2 years will be ideal
  • Looking for biology or microbiology, but any really of those extensions, if they have lab skills or have done plating and dilution working with microorganisms.
  • Masters, if they have maybe one year of experience would probably be OK, but PHD may be overqualified for this level.
  • Academic lab experience be considerable

Interview process: 2 interviews ย (Teams and Onsite, Length, Rounds, Team involved) Teams, one round, two team members involved, 30-45 minutes.