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Protocol Associate Jobs in North Carolina (NOW HIRING)

The Laboratory Associate I will execute protocols under the direct supervision of the Director, R&D. How you will make an impact: * Receive, label, store, and report customer samples. * Perform ...

Complex Commercial Litigation Associate Attorney Location: Raleigh, NC (On-site / Hybrid) Salary ... Supervise complex written discovery protocols, oversee third-party subpoena workflows, and manage ...

Postdoctoral Associate - Translational Microbiome and Critical Care Research The Duke ... and other protocol-specified samples. • Performing light sample processing, labeling ...

Sales Associate

Charlotte, NC · On-site

$13.50 - $18.25/hr

... protocols. Actively identify opportunities to streamline workflows and improve efficiency to meet ... Associates must be willing to work a flexible schedule based on business needs, which will include ...

Warehouse Associate Location: Lexington, NC Pay Rate: $17.00 per hour Schedule: Monday Friday, 8:00 ... Inspect equipment before use and adhere strictly to all OSHA and facility safety protocols ...

Warehouse Associate Location: Lexington, NC Pay Rate: $17.00 per hour Schedule: Monday - Friday, 8 ... Inspect equipment before use and adhere strictly to all OSHA and facility safety protocols ...

You're the people we trust to protect our associates, our customers, and the thousands of vehicles ... From clearing snow during a winter storm to running heat-safety protocols in July, you'll be the ...

You're the people we trust to protect our associates, our customers, and the thousands of vehicles ... From clearing snow during a winter storm to running heat-safety protocols in July, you'll be the ...

You're the people we trust to protect our associates, our customers, and the thousands of vehicles ... From clearing snow during a winter storm to running heat-safety protocols in July, you'll be the ...

Showing results 41-60

Protocol Associate information

What is a protocol associate?

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 does a protocol associate do?

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?

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 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.

What are the most commonly searched types of Protocol jobs in North Carolina?

The most popular types of Protocol jobs in North Carolina are:

What cities in North Carolina are hiring for Protocol Associate jobs?

Cities in North Carolina with the most Protocol Associate job openings:

Laboratory Associate I

Cygnus Technologies

Leland, NC • On-site

Full-time

Medical, Retirement, PTO

This job post has expired 4 days ago. Applications are no longer accepted.


Job description

Who we are:
Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.
At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market.
Your next role as a Miracle Maker
Maravai LifeSciences is seeking a #MiracleMaker to join our Custom Development team as a Laboratory Associate I. As a Laboratory Associate I, you will be responsible for lab bench sample preparation, chromatography, large format 2D-electrophoresis, spot counting, data analysis, and report writing and review. Demonstrated working knowledge of lab-based research, method development, testing, custom services life science or pharmaceutical industrial application is preferred. The Laboratory Associate I will execute protocols under the direct supervision of the Director, R&D.
How you will make an impact:
  • Receive, label, store, and report customer samples.
  • Perform chromatography of customer samples via FPLC and 2D-PAGE.
  • Analyze 2D-PAGE data with spot counting software and write reports.
  • Author SOPs and develop new data analysis tools.
  • Maintain lab instruments and consumable steady state levels.
  • Maintaining sample inventory and defrosting refrigerators and freezers.
  • Dispose of hazardous chemicals in compliance with EHS.
  • Place purchase orders via ERP software.
  • Record data in lab notebooks and data binders.
  • Present data at lab meetings.
  • Perform buffer exchange and sample concentrations.
  • Develop and optimize workflows.
  • Prepare LC solvents in scheduled intervals.
  • Perform other functions and duties as required.

The skills and experience that you will bring:
  • Degree in Biochemistry, Biology, Chemistry or similar Life Science
    • Associate degree with 2 years or BS and 1 year of biotechnology industry experience
  • Experience documenting work in laboratory notebooks; GLP/GDP experience a plus.
  • Experience running FPLC; executing protocols and analyzing data a plus
  • Excellent written/verbal communication skills.
  • Proficiency with Microsoft Office products; PowerPoint, Excel, Word, ...

#LI-Onsite
The benefits of being a #MiracleMaker:
  • You have the potential to change, improve, and save lives around the world.
  • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans.
  • We offer comprehensive medical plans and HSA/FSA options.
  • Fertility & family planning assistance.
  • A variety of additional optional benefits and insurance options, including pet insurance.
  • Retirement contributions.
  • Holidays & Paid Time Off.

Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/
To view more opportunities to become a #MiracleMaker, visit our career site at https://www.maravai.com/careers/
Cygnus Technologies, a Maravai LifeSciences company, is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
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If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov.