CrawlJobs Logo

Research Associate - Certified Phlebotomy Technician

parexel.com Logo

Parexel

Location Icon

Location:
United States , Glendale

Category Icon
Category:
-

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

20.00 - 26.00 USD / Hour

Job Description:

Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and “first in human” trials are the first step in testing these novel treatments in humans. At Parexel Glendale, CA unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally.

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
  • 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
  • Comply with Quality Management (QM) department guidelines and perform corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner

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
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
  • Other benefit offerings in accordance with the terms of applicable plans

Additional Information:

Job Posted:
January 09, 2026

Employment Type:
Parttime
Work Type:
On-site work
Job Link Share:

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

Briefcase Icon

Similar Jobs for Research Associate - Certified Phlebotomy Technician

Research Associate - Certified Phlebotomy Technician

Parexel Early Phase Clinical Unit supports the development of innovative new med...
Location
Location
United States , Glendale
Salary
Salary:
20.00 - 26.00 USD / Hour
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Research Associate - Certified Phlebotomy Technician

Parexel Early Phase Clinical Unit supports the development of innovative new med...
Location
Location
United States , Glendale
Salary
Salary:
20.00 - 26.00 USD / Hour
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Phlebotomy Coordinator

The University of Kansas Health System Phlebotomy Coordinator is a position with...
Location
Location
United States , Kansas City
Salary
Salary:
Not provided
kansashealthsystem.com Logo
The University of Kansas Health System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High School Graduate
  • 2 or more years experience with advanced level of skill in adult and pediatric phlebotomy
  • Certified Phlebotomy Technician (CPT) - National Healthcareer Association (NHA) within 180 Days
Job Responsibility
Job Responsibility
  • Oversees daily activities of phlebotomists
  • Coordinates workflow to ensure timely collection of specimens
  • Serves as technical expert for all collection procedures
  • Orients and trains new hires
  • Performs 6 month and annual competency for Phlebotomy staff
  • Oversees proper collection of research or esoteric lab test kits
  • Manages and coordinates sick and tardy calls from staff
  • Assists manager with implementing schedule changes
  • Participates in survey readiness activities
  • Reviews selected policies and procedures
  • Fulltime
Read More
Arrow Right

Medical Research Associate

Medical Research Associate - Full Time - Monday - Friday - Salt Lake City, Utah ...
Location
Location
United States , Salt Lake City
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Read, write, and speak English
  • fluent in host country language required
  • High School Diploma or G.E.D. required
  • Undergraduate degree in a clinical, health-related area and/or minimum 1 year of equivalent work experience with similar position
  • 1+ years work experience in a medical or clinical field preferred
  • Basic Life Support (BLS)/Phlebotomist Certification preferred
  • Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred
Job Responsibility
Job Responsibility
  • Meet/greet clinical research volunteers as they come into the clinic
  • Check vitals (height, weight, blood pressure, BMI)
  • Ensure study participants are healthy enough to participate in the clinical trial according the protocol
  • Perform basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment, obtain medical history and assists with Investigational Product accountability
  • Ensure all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements
  • Perform non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc
  • Monitor subject safety
  • Report equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies
  • Perform general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc
  • Assist with study setup activities and perform check-in and check-out activities
What we offer
What we offer
  • Comprehensive and competitive total reward package
  • Excellent level of base pay
  • Wide range of variable pay and recognition programs
  • Best in class employee benefits
  • Supportive policies
  • Wellbeing initiatives tailored to support you and your family at all stages of your career
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
  • Fulltime
Read More
Arrow Right

Medical Research Associate

Clinical Research - Medical Research Associate, Full Time w/ Benefits, Day Shift...
Location
Location
United States , Salt Lake City
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A strong command of both English and the host country's language is essential
  • A High School Diploma or G.E.D. qualification
  • If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role
  • 1+ years of work experience in a medical or clinical field is preferred
  • If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
  • Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
Job Responsibility
Job Responsibility
  • Meeting/greeting clinical research volunteers as they come into the clinic
  • Checking their vitals (height, weight, blood pressure, BMI)
  • Performing phlebotomy
  • Making sure the study participants are healthy enough to participate in the clinical trial according to the study protocol
  • Taking vital signs and performing phlebotomy on study subjects
  • Following our clients' protocols when conducting vital sign assessments and phlebotomy procedures
  • Active participation in meetings and other assignments
  • Chaperone study subjects during their breaks outside
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments
  • Fulltime
Read More
Arrow Right

Research Associate

Parexel Early Phase Clinical Unit supports the development of innovative new med...
Location
Location
United States , Glendale
Salary
Salary:
20.00 - 26.00 USD / Hour
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right
New

General Operative

We are looking for a reliable General Operative to join our production team in a...
Location
Location
United Kingdom , Swindon
Salary
Salary:
12.00 - 13.00 GBP / Hour
https://www.randstad.com Logo
Randstad
Expiration Date
April 27, 2026
Flip Icon
Requirements
Requirements
  • GCSE Maths and English (Grade C/4 or above) or equivalent
  • Previous experience in a regulated industry (Food, Pharma, Auto, or Engineering) is preferred but not essential
Job Responsibility
Job Responsibility
  • Cleanroom Support: Following strict gowning and hygiene procedures to enter production areas
  • Production Tasks: Assisting with packaging, labeling, and weighing products
  • Maintenance: Cleaning equipment and production areas according to standard operating procedures (SOPs)
  • Material Handling: Moving stock, checking expiry dates, and loading equipment like washers or autoclaves
  • Documentation: Keeping accurate, clear records of all work completed
Read More
Arrow Right
New

Reach Truck Driver

Are you an experienced Reach Truck Driver looking for a new challenge at Kuehne+...
Location
Location
Belgium , Tessenderlo
Salary
Salary:
Not provided
https://www.randstad.com Logo
Randstad
Expiration Date
September 29, 2026
Flip Icon
Requirements
Requirements
  • Valid Reach Truck certificate
  • Proven experience operating a reach truck, preferably in a warehouse environment with high racking
  • Willingness to work in a 2-shift system in the Tessenderlo area
  • Flexibility to perform weekend work during peak periods when required
  • Strong sense of responsibility regarding workplace safety and quality
Job Responsibility
Job Responsibility
  • Stock Management: storing and retrieving DIY products using the reach truck
  • High-Level Picking: picking goods at significant heights and ensuring they are ready for shipment without any damage
  • Inventory Control: performing regular stock checks to maintain inventory accuracy
  • Operational Support: supporting the general warehouse operations at Kuehne+Nagel whenever necessary
  • Safety Standards: strictly adhering to the rigorous safety regulations that apply to every Reach Truck Driver on site
  • Fulltime
Read More
Arrow Right