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Part Time Product Research Jobs (NOW HIRING)

MBA Internship

Alameda, CA ยท On-site +1

$17 - $22.75/hr

... our strategy, product, and growth initiatives. This is a part-time internship averaging ... Conduct market research and competitive analyses to identify emerging opportunities in maritime ...

$13.75 - $17/hr

Kristina Petersen's lab in the Department of Nutritional Sciences is seekingdynamic part-time research assistants to join our highly productive research kitchen for the summer (May to August 2026)

PART-TIME PRODUCTION ADMIN

Lewisville, TX ยท On-site

$15.50 - $19.25/hr

The Part-Time Production Administrator provides administrative and production support to the ... Research and resolve discrepancies in labor reporting and job hour allocations. Manufacturing ...

PART-TIME PRODUCTION ADMIN

Lewisville, TX ยท On-site

$20 - $24/hr

Job Type Part-time Description The Part-Time Production Administrator provides administrative and ... Research and resolve discrepancies in labor reporting and job hour allocations. Manufacturing ...

Hourly Research Assistants

Campus, IL ยท On-site

$17 - $25/hr

No Standard Hours per Week up to 19 hours Full Time or Part Time? Part Time Shift Day Work Schedule ... Serves as the primary individual responsible for the day-to-day preparation and production of ...

Showing results 21-40

Part Time Product Research information

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$10

$27

$58

How much do part time product research jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for part time product research in the United States is $27.21, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $33.65 per hour, depending on experience, location, and employer.

What is the difference between Part Time Product Research vs Part Time Market Analyst?

AspectPart Time Product ResearchPart Time Market Analyst
Required CredentialsTypically a bachelor's degree in marketing, business, or related fieldsUsually a bachelor's degree in marketing, economics, or business
Work EnvironmentResearch firms, product development teams, or online platformsMarket research firms, consulting agencies, or corporate marketing departments
Employer & Industry UsageUsed across consumer goods, tech, and retail industries for product insightsCommon in finance, retail, and consulting sectors for market trends analysis

Part Time Product Research focuses on gathering data to inform product development, while Part Time Market Analyst examines broader market trends. Both roles require similar educational backgrounds and often operate in related industries, but their core functions differ in scope and focus.

How to become a part time product researcher?

To become a part-time product researcher, you typically need strong analytical skills, familiarity with market research tools, and the ability to evaluate product trends. Relevant experience or education in business, marketing, or related fields can be beneficial, and many roles require self-motivation and good time management for flexible schedules.
More about Part Time Product Research jobs

What are the most commonly searched types of Product Research jobs?

The most popular types of Product Research jobs are:

What are popular job titles related to Part Time Product Research jobs?

For Part Time Product Research jobs, the most frequently searched job titles are:

Infographic showing various Part Time Product Research job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $56,597 per year, or $27.2 per hour.

Clinical Research Coordinator (Part-time)

Somers Point, NJ โ€ข On-site

Tandem Clinical Research
Scientific Research and Development Servicesย โ€ขย 11 - 50 employees

$24.75 - $32.75/hr

Part-time

Re-posted 17 days ago


Key responsibilities

  • Oversee and manage the daily operational activities of assigned clinical research studies.

  • Coordinate study start-up activities, including feasibility, regulatory submissions, and site activation.

  • Monitor and assess study subjects, manage documentation and data entry, and ensure compliance with protocols and regulatory requirements.


Job description

Clinical Research Coordinator (CRC)
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.
The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
Key Responsibilities
Study Management & Coordination
  • Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
  • Support study start-up activities including feasibility, regulatory submissions, and site activation.
  • Attend investigator meetings, site initiation visits, and other study-related meetings.
  • Manage visit schedules and coordinate study-related activities across clinical teams.

Recruitment, Enrollment & Consent
  • Collaborate with recruitment teams to support participant screening and enrollment.
  • Conduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.
  • Ensure protocol and regulatory requirements are met throughout the enrollment process.

Clinical Oversight & Subject Monitoring
  • Monitor and assess study subjects in accordance with protocol requirements.
  • Identify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.
  • Escalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.

Documentation, Data & Systems
  • Maintain accurate and complete source documentation, case report forms, regulatory files, and study records.
  • Enter study data into EDC and other required systems and manage study databases.
  • Complete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.
  • Report protocol deviations to the PI, sponsor, and IRB as required.

Investigational Product & Specimen Management
  • Manage investigational product accountability records and documentation.
  • Collect, process, package, and ship study specimens per protocol requirements.
  • Perform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.

Quality, Compliance & Team Support
  • Ensure all study activities comply with SOPs, GCP, and regulatory requirements.
  • Support quality assurance activities and audit readiness.
  • Provide assistance and mentorship to fellow coordinators as needed.
  • Maintain strict confidentiality of participant and study information.

Communication & Outreach
  • Serve as the primary point of contact for sponsor and CRO communications.
  • Participate in occasional outreach or community events related to clinical trials.
  • Ensure timely, accurate communication of study updates and issues.

Additional Responsibilities
This job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.
Requirements
  • Knowledge, Skills, and Abilities
  • Strong leadership and communication skills
  • Exceptional organizational and multitasking abilities
  • High attention to detail and commitment to regulatory compliance
  • Ability to work independently and collaboratively in a multidisciplinary environment
  • Strong time management and operational efficiency skills
  • Proficiency with office equipment and study-specific systems
  • Ability to maintain strict confidentiality
  • Required Experience & Qualifications
  • Education: Bachelor's degree in a related field
  • Experience: Minimum of two (2) years of clinical research or clinical trial management experience
  • Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)
  • Phlebotomy: Prior experience performing blood draws and handling biological specimens required