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Cog Program Manager Jobs (NOW HIRING)

Program Assistant 4

Evanston, IL · On-site

$21.48 - $27.69/hr

Department: MED-Mesulam Ctr Cog Neur & Alz Salary/Grade: NEX/12 Target hiring range for this ... Manages supervisor's &/or dept calendar. * Manages complex scheduling arrangements involving ...

Program Assistant 4

Chicago, IL · On-site

$21.48 - $27.69/hr

... Mesulam Ctr Cog Neur & Alz Salary/Grade: NEX/12 Target hiring range for this position will be ... Manages supervisor's &/or dept calendar. * Manages complex scheduling arrangements involving ...

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... Ohio COG Mason, OH | Full-Time | School-Year Schedule Warren County ESC/Southwest Ohio COG is ... management and student engagement * Collaborate with teachers and multidisciplinary staff Program ...

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Cog Program Manager information

See salary details

$30K

$71.3K

$109.5K

How much do cog program manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for cog program manager in the United States is $71,266.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $80,000.00 per year, depending on experience, location, and employer.

What is a Cog Program Manager?

A Cog Program Manager is responsible for overseeing and coordinating programs related to cognitive (Cog) technologies, such as artificial intelligence, machine learning, or automation within an organization. They manage project timelines, resources, and cross-functional teams to ensure successful implementation of cognitive solutions. Their role often involves strategic planning, stakeholder communication, and ensuring that projects align with business goals. Cog Program Managers also track progress, manage risks, and ensure the delivery of high-quality outcomes for cognitive initiatives.

What are the typical responsibilities of a Cog Program Manager and how do they collaborate with cross-functional teams?

A Cog Program Manager is generally responsible for overseeing the planning, execution, and delivery of projects within cognitive (Cog) computing or AI-driven programs. This role involves coordinating with data scientists, software engineers, product managers, and stakeholders to ensure project milestones are met on time and within budget. Cog Program Managers are often tasked with risk management, resource allocation, and progress reporting, while facilitating communication between technical and non-technical teams. Regular collaboration with various departments ensures alignment on project goals and the successful integration of cognitive solutions into broader business strategies.

What are the key skills and qualifications needed to thrive as a Cog Program Manager, and why are they important?

To thrive as a Cog Program Manager, you need strong project management skills, experience in process optimization, and a background in business or operations management, often supported by a relevant degree. Familiarity with tools like Microsoft Project, JIRA, and Lean Six Sigma certification is commonly required. Excellent leadership, communication, and problem-solving abilities enable you to coordinate teams and drive program objectives effectively. These skills are vital to ensure smooth program execution, stakeholder alignment, and the achievement of organizational goals.

What is the difference between Cog Program Manager vs Cog Project Coordinator?

AspectCog Program ManagerCog Project Coordinator
CredentialsTypically requires a bachelor's degree in a related field; certifications like PMP are commonUsually requires a bachelor's degree; certifications are less common
Work EnvironmentOversees multiple projects within a program, often in corporate or government settingsSupports project teams, manages schedules, and assists in project execution
ResponsibilitiesStrategic planning, coordinating multiple projects, ensuring program goals are metAssists with project tasks, tracks progress, and communicates between teams

The Cog Program Manager focuses on managing multiple projects within a program, ensuring strategic alignment and overall success. In contrast, the Cog Project Coordinator handles specific project tasks, supporting project managers and teams to meet project deadlines. Both roles require strong organizational skills, but the Program Manager has a broader, more strategic scope.

What are popular job titles related to Cog Program Manager jobs?

For Cog Program Manager jobs, the most frequently searched job titles are:

Infographic showing various Cog Program Manager job openings in the United States as of June 2026, with employment types broken down into 75% Part Time, and 25% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $71,266 per year, or $34.3 per hour.

Clinical Research Coordinator (CRC)

Kalamazoo, MI • On-site

$44/hr

Contractor

Medical

Re-posted 8 days ago


Key responsibilities

  • Prepare, submit, and monitor documentation for research programs.

  • Ensure compliance with research regulations and protocols through audits.

  • Coordinate enrollment of participants into Children's Oncology Group (COG) studies.


Job description

3 - 6 Month Contract

Potential (Temp-to-Hire)


Fully Onsite

Monday - Friday

8:00 am - 5:00 pm


M-F 8am-5pm
FULLY On-site
Temp to hire
Qualifications & Requirements:

  • Must have previous experience with COG
  • Bachelor's degree in a scientific or healthcare field, or equivalent experience in Data entry, Research, Healthcare administration education in the protection of human research participants and Good Clinical Practices required.


Current clinical licensure and board certifications:

  • SOCRA (preferred)
  • ACRP (preferred within 4 years of hire)
  • CITI training
  • Human protections training
  • IATA certification for shipping infectious substances and diagnostic specimens.

Ability to read and interpret:

  • Research documents
  • Clinical trial documents
  • Operating and maintenance instructions
  • Procedure manuals
  • Strong written and verbal communication skills.
  • Excellent interpersonal and relationship-building skills.

Ability to work effectively with:

  • Physicians
  • Physician offices
  • Sponsors
  • Hospital employees
  • Strong analytical and problem-solving abilities.

Ability to work efficiently under:

  • Tight deadlines
  • High workloads
  • Frequent interruptions
  • Strong attention to detail and adherence to clinical trial requirements.

Clinical Research Coordinator – Key Responsibilities

  • Prepare, submit, and monitor documentation for research programs.
  • Ensure compliance with research regulations and protocols through audits.
  • Advise caregivers on program design, treatment administration, and patient follow-up.
  • Organize study files, including regulatory binders and source documentation.
  • Maintain and update study files and records according to sponsor and institutional requirements.
  • Review, edit, and update informed consent documents for clinical trials.
  • Collaborate with the Principal Investigator (PI) to prepare IRB and regulatory submissions.
  • Assist in reviewing eligibility criteria for participant enrollment.
  • Coordinate enrollment of participants into Children's Oncology Group (COG) studies.
  • Develop familiarity with COG protocols and specimen submission guidelines.
  • Collect study data and ensure timely completion of Case Report Forms.
  • Coordinate audits with the central COG office and maintain audit readiness.
  • Perform additional duties as assigned.

Physical & Work Environment Requirements

  • Work is mentally and visually demanding for more than 90% of the work time.
  • Requires considerable standing and walking.
  • Requires lifting light objects (up to approximately 20 pounds).
  • May involve assisting with lifting or moving patients.
  • Requires maintaining potentially fatiguing positions and performing repetitive physical movements.

Clinical Research Coordinator (CRC):

  • For all new Trials, confirm if DTL must be created and if slide deck training is required
  • Take primary responsibility for early specimen/x-ray/lab submission for RAPID EARLY Review
  • Obtain parental consent for APEC14B1 (parental DNA and part B if needed)
  • Maintain BMH compliance Spreadsheets with updates (quarterly, on SharePoint)
  • Track patients on study and in follow-up
  • Maintain Outlook Calendar for upcoming time points/appointments
  • Complete all CRFs for Baseline, Reporting Period and Follow-up folders for all patients.
  • Monitor SADD list weekly
  • Attend daily check-in and chemotherapy rounds
  • Collect all patient documents for diagnosis and treatment courses
  • Prepare AE flow sheets for each therapeutic trial
  • Attend CRCWM Pediatric Protocol reviews first Thursday every month at 0700
  • Know investigational agents and how to get them (drug ordering)
  • Prepare charts for AUDIT, attend COG meetings

Clinical Research Coordinator (CRC) and Clinical Research Assistant (CRA):

  • CITI training/Human Protections training
  • Dangerous Goods training
  • Patient Registration
  • Confirming eligibility/ Fast Facts reviewed
  • Review all consents for correct signatures/initials on day signed
  • Attend weekly COG working group meetings
  • Attend Teams meetings with Helen DeVos Children’s Hospital every 2 weeks


Maintain active account access and training for:

  • iMedidata/Rave
  • COG/eRDS
  • CTSU/OPEN
  • Redcap*
  • TRIAD*
  • CRCWM

Company Description

AlphaProTemps is specialized in providing "best-in-class" professional staff augmentation services. These recruiting directives include temporary labor, contract sourcing, professional & technical niches, vendor-on-site, and managed service programs.