Phlebotomist III

Experis Technology Group; Sunnyvale (CA); On-site; USD 33,000 - 36,000; Full time

Job summary

ManpowerGroup Global, Inc. is seeking a Phlebotomist III to join a leading healthcare client in Santa Clara, CA. This 12-month, 100% onsite contract focuses on collecting blood specimens for research analysis and testing, with independence and strong task management required.

Required qualifications include an accredited phlebotomy program and CPT certification, 2–5 years of phlebotomy or clinical research experience, and proficiency in venipuncture, data recording, and regulatory compliance.

Qualifications

• Associate or bachelor’s degree in a health or science-related field preferred.
• Completion of an accredited phlebotomy training program.
• 2–5 years of phlebotomy or clinical research experience preferred.

Responsibilities

• Collect blood specimens from subject donors.
• Recruitment, screening, and informed consent processes.
• Schedule study visits and specimen collection timelines.
• Document study-related data in electronic or paper case report forms.
• Ensure compliance with study protocols, IRB guidelines, and regulatory requirements.
• Communicate effectively with study participants, investigators, OHN, and clinical teams.
• Perform blood sample testing as required.

Skills

Venipuncture

Specimen handling

Organization

Time management

Communication

Independence

Collaboration

GCP/GDP

Education

Health/Science degree

Job description

Job Title: Phlebotomist III

Location: Santa Clara, CA 94085

Duration: 12 months

Work Arrangement: 100% Onsite

Pay Range: $24 - $26 per hour (W2)

We are seeking a “Phlebotomist III” to join one of our leading healthcare clients.

Description:

The Phlebotomist III/Research Study Staff member is responsible for collecting blood specimens from subject donors within the facility for research analysis or testing purposes. The individual must be capable of working independently, demonstrating strong initiative, sound judgment, and the ability to manage tasks with minimal supervision.

Additional responsibilities include:

• Assisting with participant recruitment, screening, and the informed consent process.
• Scheduling and coordinating study visits and specimen collection timelines.
• Accurately documenting study-related data in electronic or paper case report forms.
• Ensuring compliance with study protocols, IRB guidelines, and regulatory requirements.
• Communicating effectively with study participants, investigators, Occupational Health Nurses (OHN), and clinical teams.
• Performing blood sample testing as required.

Qualifications:

• Associate or bachelor’s degree in a health or science-related field preferred.
• Completion of an accredited phlebotomy training program.
• 2–5 years of experience in phlebotomy and/or clinical research preferred.

Skills & Competencies:

• Proficient in venipuncture/capillary blood collection and specimen handling techniques.
• Strong organizational and time management skills.
• Familiarity with clinical research protocols, Good Clinical Practice (GCP) and Good Documentation Practice (GDP).
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively in a fast-paced research environment.

Certification(s):

• Certified Phlebotomy Technician (CPT) or equivalent (required).

We are looking for the candidate who are eligible to work with any employers without sponsorship