Study participant Job at Prolific

Research Associate - Certified Phlebotomy Technician

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale

Salary:

20.00 - 26.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Active CPT License in the state of CA is required
Customer service experience in a fast-paced environment
Experience working in a medical or clinical setting is highly preferred
Comfortable standing and walking for a prolonged period of time
B.S.+ in related life science field OR HS diploma/GED with relevant experience

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Extensive induction program and ongoing training
Opportunity for career growth and advancement internally
Eligible for shift differentials
Eligible for participation in annual performance-based bonus plan
Annual salary review
Additional total rewards incentives
Paid time off
401k match
Life insurance
Health insurance

Fulltime

Research Associate

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale

Salary:

20.00 - 26.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Customer service experience in a fast-paced environment
Clinical Research experience or patient experience is required
B.S.+ in related life science field OR HS diploma or GED with experience
Comfortable standing and walking for a prolonged period of time
Certified Phlebotomy Technician I License is required

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Paid time off
401k match
Life insurance
Health insurance
Other benefit offerings
Annual performance-based bonus plan (for eligible roles)
Annual salary review
Additional total rewards incentives (for eligible roles)
Extensive induction program
Ongoing training

Fulltime

Research Associate - Certified Phlebotomy Technician

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale

Salary:

20.00 - 26.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Active CPT License in the state of CA is required
Customer service experience in a fast-paced environment
Experience working in a medical or clinical setting is highly preferred
Comfortable standing and walking for a prolonged period of time
B.S.+ in related life science field OR HS diploma/GED with relevant experience

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Paid time off
401k match
Life insurance
Health insurance
Other benefit offerings in accordance with the terms of applicable plans
Annual performance-based bonus plan (for eligible roles)
Annual salary review
Additional total rewards incentives (for eligible roles)
Extensive induction program
Ongoing training

Parttime

Research Associate

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale, California

Salary:

20.00 - 27.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Customer service experience in a fast-paced environment
Clinical Research experience or patient experience is required
B.S.+ in related life science field OR HS diploma or GED with experience
Comfortable standing and walking for a prolonged period of time
Required: fluent in spoken and written English as well as Mandarin

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Extensive induction program and ongoing training
Career advancement support
Market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings
Annual performance-based bonus plan (for eligible roles)
Annual salary review
Additional total rewards incentives (for eligible roles)

Research Associate - Certified Phlebotomy Technician

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale

Salary:

20.00 - 26.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Active CPT License in the state of CA is required
Customer service experience in a fast-paced environment
Experience working in a medical or clinical setting is highly preferred
Comfortable standing and walking for a prolonged period of time
B.S.+ in related life science field OR HS diploma/GED with relevant experience

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Extensive induction program and ongoing training
Opportunity for career growth and advancement
Eligible for shift differentials
Eligible for participation in annual performance-based bonus plan (for eligible roles)
Annual salary review
Additional total rewards incentives
Paid time off
401k match
Life insurance
Health insurance

Parttime

Senior Human Sub Research Spec

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

60431.00 - 84603.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 5 years of experience in human subject coordination required
Or equivalent combination of education and experience
Phlebotomy skills for adult and pediatric patients and good computer skills Required
Independent and organized professional with superior interpersonal skills, sound judgment and good oral and written communication skill
Strong attention to detail and must be able to problem-solve effectively. Required
Knowledge of computer databases including eRecord and ePARC, Word and Excel software programs. Required

Job Responsibility

Participate in ongoing research studies in the Urology Clinical Trials Office relating to Oncology and General Urology. phase 1-3 industry and Investigator initiated studies, in therapeutic agents in adult populations.
Conducts unstructured interviews with subjects and families as required by protocol
perform clinical research related procedures (blood draws and sponsor specific delegated responsibilities)
measures, records, and reports indicators of patient health status
perform more specialized tasks such as Bladder Scans, pad weight tests, ECGs and Uroflowmetry
evaluates subjects for local or systemic reactions to determine adverse events to study medication.
Discuss with subjects’ potential adverse events and SAEs and participating in grade of events.
Participate in the reporting of subject serious adverse events (SAE) and filing of these in a timely manner to sponsors and IRBs.
Identification of subject pool, eligibility screening in clinic settings and/or telephone screens
medical history review

Fulltime

Research Associate

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Baltimore

Salary:

20.00 - 22.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Proven customer service experience in a fast-paced environment
Background working in a medical or clinical setting
Comfortable with prolonged periods of standing and walking
B.S.+ in related life science field OR HS diploma/GED with relevant experience
CPT/Phlebotomy is highly preferred
Minimum availability requirements: 16 hours of availability per week AND two 12-hour weekend shifts in a 4-week month OR three 12-hour weekend shifts in a 5-week month
First 4 to 6 weeks required to work 40 hours a week for training (day shift - 6:50am to 3:20pm)

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Maintain and update knowledge of Clinical Operating Guidelines and their proper application
Assume appropriate role with study participants and caregivers
Assure quality and accuracy of source and CRF documentation

What we offer

Paid time off
401k match
Life insurance
Health insurance
Other benefit offerings in accordance with the terms of applicable plans
Potential participation in annual performance-based bonus plan
Annual salary review
Additional total rewards incentives

Parttime

Research Associate

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Baltimore

Salary:

20.00 - 22.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Proven customer service experience in a fast-paced environment
Background working in a medical or clinical setting
Comfortable with prolonged periods of standing and walking
B.S.+ in related life science field OR HS diploma/GED with relevant experience
CPT/Phlebotomy is highly preferred
Minimum availability requirements: 16 hours of availability per week AND two 12-hour weekend shifts in a 4-week month OR three 12-hour weekend shifts in a 5-week month
Required Training: First 4 to 6 weeks required to work 30 to 40 hours a week for training (day shift - 6:50am to 3:20pm)

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Maintain and update knowledge of Clinical Operating Guidelines and their proper application
Assume appropriate role with study participants and caregivers
Assure quality and accuracy of source and CRF documentation

What we offer

Market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans
Some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and additional total rewards incentives

Parttime

Study participant

Prolific

Location:
Ireland

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 07, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Study participant

Research Associate - Certified Phlebotomy Technician

Research Associate

Research Associate - Certified Phlebotomy Technician

Research Associate

Research Associate - Certified Phlebotomy Technician

Senior Human Sub Research Spec

Research Associate

Research Associate

Study participant

Prolific

Location:Ireland

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 07, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Study participant

Research Associate - Certified Phlebotomy Technician

Research Associate

Research Associate - Certified Phlebotomy Technician

Research Associate

Research Associate - Certified Phlebotomy Technician

Senior Human Sub Research Spec

Research Associate

Research Associate

Location:
Ireland

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
January 07, 2026