Phlebotomist - Part Time

About the role

Kelly Science & Clinical is seeking a Part-Time Phlebotomist to support research activities within a leading pharmaceutical and life sciences organization located in Spring House, PA. This is a great opportunity for an experienced phlebotomist looking for a consistent part-time schedule in a research-focused environment.

Schedule

Part-time: 3 days per week

• Days: Monday, Tuesday, Wednesday and/or Thursday
• Candidates may choose which three days they work, but the schedule must remain consistent.
• Hours: 7:30 AM – 12:30 PM
• Weekly Hours: 15 hours

Responsibilities

• Perform venipuncture and collect human biological samples according to approved research protocols.
• Use an electronic donor scheduling system to manage daily schedules, sample requests, volunteer information, and daily work activities.
• Administer informed consent forms to clinical trial volunteers and address questions as appropriate.
• Accurately document and track sample collections using required FDA tracking logs.
• Perform data entry, record keeping, records management, and document archiving.
• Maintain accurate and complete documentation in accordance with established procedures.
• Perform quarterly laboratory safety checks.
• Maintain strict confidentiality and protect the privacy and anonymity of research volunteers.
• Communicate issues or concerns to the supervisor in a timely manner.
• Maintain knowledge of current methods and techniques relevant to phlebotomy and specimen collection.
• Maintain current First Aid/CPR certification.
• Follow all applicable GxP, FDA, EHSS, OSHA, HIPAA, and IRB requirements.
• Work under supervision while demonstrating day-to-day autonomy.
• Perform other duties as assigned.

Qualifications

• Previous experience performing venipuncture and blood specimen collection.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Strong computer skills, including Microsoft Word, Excel, and Teams.
• Ability to accurately maintain records and complete documentation.
• Ability to follow SOPs, research protocols, and regulatory requirements.
• Current First Aid/CPR certification or ability to maintain certification as required.

Preferred Qualifications

• Experience in a clinical research, laboratory, pharmaceutical, biotechnology, or healthcare environment.
• Experience working with electronic scheduling or clinical trial systems.
• Familiarity with GxP, FDA, HIPAA, OSHA, EHSS, or IRB requirements.
• Experience collecting and documenting research specimens.