Study participant Job at Prolific

Clinical Research Assistant

The Division of Genetics and Genomics at Boston Children’s Hospital is seeking a...

Location

United States , Boston

Salary:

41246.40 - 61339.20 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree
Strong quantitative and analytical skills
comfortable with numbers
Interested in working with children and adults with severe physical and intellectual disabilities, and their families
Excellent interpersonal as well as oral and written communication skills
Willingness to work flexible hours, as and when required

Job Responsibility

Assisting Principal Investigator (PI) in planning and implementing clinical research studies as assigned, including: coordinating preparation of protocol applications for submission to the IRB, study sponsor, regulatory authority, etc.
corresponding with the IRB, study sponsors, clinical research organizations, study participants, and referring physicians
Recruiting study participants for enrollment in clinical studies, including organizing strategies for recruiting study participants, screening study participants for eligibility, and completing informed consent procedures
Organizing study procedures and scheduling study participants for study visits. Assists the PI during study visits
Completing record abstraction of source documents, conducting required study measurements and completing study Case Report Forms (CRFs)
conducting a QC check of completed CRFs prior to submission for data entry
coordinating resolution of all data queries
Maintaining regulatory binders, case report forms, source documents, and other study documents
monitoring the occurrence of adverse events and reporting to the PI, the study sponsor and the IRB, if any
Under the supervision of the PI, work with study staff to prepare for monitoring and audits by independent monitors, sponsors, and other regulatory agencies

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

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 - 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

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.

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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