Study participant Job at Prolific

New

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

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

New

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

New

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

Clinical Trial Manager

The Clinical Trial Manager is responsible for the overall management of clinical...

Location

Salary:

Not provided

KGTiger

Expiration Date

Until further notice

Requirements

Master’s degree in a related field, such as clinical research, biostatistics, or epidemiology
Experience in clinical trial management
Strong organizational and time management skills
Excellent communication and interpersonal skills
Ability to work independently and as part of a team
Proficient in Microsoft Office Suite
Experience with a variety of clinical research software programs.
Strong understanding of clinical trial principles and practices
Excellent organizational and time management skills
Excellent written and verbal communication skills

Job Responsibility

Plan and manage clinical trials. This includes developing trial protocols, recruiting participants, and overseeing the conduct of trials
Ensure that trials are conducted ethically and in accordance with regulations. This includes reviewing study protocols and ensuring that they meet ethical standards, and monitoring the conduct of trials to ensure that they are conducted in accordance with regulations
Oversee the conduct of trials. This includes ensuring that trials are conducted according to the study protocol, resolving any issues that arise during the course of a trial, and ensuring that trials meet their objectives
Report on the progress of trials. This includes providing regular reports to stakeholders, such as the study sponsor, regulatory agencies, and ethics committees
Communicate with stakeholders. This includes communicating with the study sponsor, regulatory agencies, ethics committees, and study participants
Advocate for the rights of study participants. This includes ensuring that study participants are treated fairly and that their rights are protected

Clinical Research Coordinator

The Clinical Research Coordinator is responsible for coordinating all aspects of...

Location

Salary:

Not provided

KGTiger

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a related field, such as biology, biochemistry, or nursing
Experience in clinical research
Strong organizational and time management skills
Excellent communication and interpersonal skills
Ability to work independently and as part of a team
Proficient in Microsoft Office Suite.
Strong understanding of clinical research principles and practices
Excellent written and verbal communication skills
Experience with regulatory compliance.

Job Responsibility

Screening and enrolling participants in clinical trials.
Collecting and managing clinical data.
Monitoring participant safety.
Administering study medications and treatments.
Coordinating with other study personnel.
Preparing and submitting study reports.
Training and supervising research staff.
Providing support to study participants.
Advocating for the rights of study participants.

New

Clinical Research Coordinator

The Fetal-Neonatal Neuroimaging and Developmental Science Center, Laboratories o...

Location

United States , Boston

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree in STEM or Psychology (or related field) is required
Master’s degree is preferred
Two years of work experience is required
Experience managing a team
Experience working with children
Well-developed communication skills
High attention to detail and organizational skills
Ability to multi-task
Analytical skills to gather and interpret data
Sensitivity in working with women, infants, and young children from various backgrounds

Job Responsibility

Assist Principal Investigators (PIs) in implementing the HBCD Study
Work with and coordinate a large research team
Manage communications with staff at collaborating sites
Assist with recruitment of study participants
Write/update study protocol/materials
Execute study visits remotely, in the lab, and in participants’ homes
Oversee data management
Attend and/or lead study-related meetings
Train collaborators off-site
Organize hiring and training of new research staff

What we offer

Flexible schedules
Affordable health, vision and dental insurance
Child care and student loan subsidies
Generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
Cell phone plan discounts
Discounted rates on T-passes

Fulltime

New

Clinical Research Assistant

The Clinical Research Assistant working in the Rheumatology and Dermatology Sect...

Location

United States , Boston

Salary:

41246.40 - 61339.20 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

A bachelor’s degree in STEM or Psychology is required
Proficiency with Microsoft Office applications (Word, Excel, Powerpoint) is required
Experience communicating or working with patients is preferred but not required
Experience with statistical programming software such as STATA, SAS, SPSS, or R is preferred but not required

Job Responsibility

Assist Principal Investigator(s) (PIs) in implementing clinical research studies
Recruit and consent study participants
Perform data collection, data entry, and data quality checks for clinical research studies
Assist in preparation of institutional review board (IRB) protocol submissions and amendments
Maintain regulatory binders, source documents, and study supplies
Assist in development and maintenance of surveys, forms, and instruments for research purposes
Participate in weekly research coordinator team meetings and present summaries of recruitment progress and study updates
Participate in annual internal study audits and ensure compliance with all institutional policies and government regulations pertaining to human subjects’ protections

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Study participant

Prolific

Location:
United States

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 07, 2026

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