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Protocol Jobs in Michigan (NOW HIRING)

McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential ...

Volto USA

EOL Calibration Engineer

Auburn Hills, MI · On-site

Proficient in CANalyzer, UDS Diagnostic protocol and services, CAN and LIN communication protocol. Roles and Responsibilities: · Interoperability testing for assigned Powertrain modules · Perform ...

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All JobsProtocol JobsProtocol Jobs in Michigan

Protocol information

See Michigan salary details

$9

$14

$17

How much do protocol jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for protocol in Michigan is $14.11, according to ZipRecruiter salary data. Most workers in this role earn between $12.55 and $15.29 per hour, depending on experience, location, and employer.

What is the difference between Protocol vs Network Technician?

AspectProtocolNetwork Technician
Required CredentialsCertifications like Cisco CCNA, CompTIA Network+Certifications like Cisco CCNA, CompTIA Network+
Work EnvironmentDesigning, implementing, and troubleshooting network protocolsInstalling, maintaining, and repairing network hardware and software
Industry UsageUsed by network engineers, administrators, and protocol developersEmployed by IT support, network service providers, and organizations
Common Search/ComparisonYesYes

While both Protocol specialists and Network Technicians work within networking environments, Protocol professionals focus on designing and managing communication rules and standards, whereas Network Technicians handle hardware setup, maintenance, and troubleshooting. Understanding these roles helps clarify career paths and job expectations in the networking industry.

What jobs pay $3,000 a day?

High-paying jobs that can reach $3,000 a day often include specialized roles such as senior corporate lawyers, top-tier management consultants, investment bankers, and certain medical specialists like surgeons. These positions typically require advanced skills, extensive experience, and often involve high-pressure environments or significant certifications. Freelance consultants or contractors in niche industries may also achieve such earnings through project-based work.

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

To thrive as a Protocol Officer, you need a solid understanding of diplomatic procedures, event planning, and cross-cultural etiquette, often supported by a degree in international relations or a related field. Familiarity with protocol guidelines, scheduling software, and communication platforms is typically required. Exceptional interpersonal skills, attention to detail, and discretion help you navigate sensitive situations and foster positive relationships. These abilities are crucial for ensuring seamless events, maintaining diplomatic decorum, and upholding an organization’s reputation.

What are protocol jobs?

Protocol jobs involve managing and coordinating official procedures, etiquette, and formalities for organizations, particularly in government, diplomatic, or large corporate settings. Professionals in these roles ensure that events, meetings, and interactions adhere to established protocols and customs, often handling VIP visits, international delegations, and ceremonial functions. Their work helps maintain positive relations, uphold organizational reputation, and ensure smooth operations during official engagements.

What are some common challenges faced by Protocol Officers when managing high-profile events?

Protocol Officers often encounter challenges such as coordinating with multiple stakeholders, ensuring that all diplomatic protocols are strictly followed, and managing last-minute changes or requests from dignitaries. Attention to detail is crucial, as even minor missteps can have significant diplomatic implications. Effective communication and adaptability are essential skills, as Protocol Officers frequently liaise with security teams, event planners, and government officials to ensure events run smoothly.
What are the most commonly searched types of Protocol jobs in Michigan? The most popular types of Protocol jobs in Michigan are:
What are popular job titles related to Protocol jobs in Michigan? For Protocol jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Protocol jobs in Michigan look for? The top searched job categories for Protocol jobs in Michigan are:
Protocol jobs near you
Clinical Research Coordinator II

Clinical Research Coordinator II

DM Clinical Research

Detroit, MI

$24 - $32/hr

Full-time

Posted 27 days ago

Job description

Clinical Research Coordinator II
The Clinical Research Coordinator II, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC II will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
Duties amp; Responsibilities:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training, as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
  • Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
  • Demonstrating adherence and compliance to the assigned protocols at their respective site(s).
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
  • Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
  • Demonstrating visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
  • Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings
  • Any other matters as assigned by management.
Knowledge amp; Experience:

Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a preferred
  • Foreign Medical Graduates preferred
Experience:
  • At least 2 years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
Credentials:
  • ACRP or equivalent certification is preferred
Knowledge and Skills:
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Bilingual in Spanish is a plus

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