Phlebotomist; Clinical Research - Per Diem

Job Category: Lab/Pharmacy

Requisition Number: PHLEB
003701

• Posted: December 11, 2025
• Part‑Time
• On‑site

Showing 1 location

Cen Exel CBH
9318 Gaither Rd.
Suite 220
Gaithersburg, MD 20877, USA

About Us:

Each of Cen Exel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long‑standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in‑patient capability.

We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Schedule:

Availability to work Monday - Friday 07:00 – 15:00, and weekend availability

Compensation: $20.00 – 21.00 /hr (depending on education, experience, and skillset)

Job Summary:

A Research Tech will obtain and prepare specimens for analysis and perform various screening tests.

• Have full knowledge of laboratory procedures and processes per protocol.
• Collect blood by drawing from patients for clinical protocols, procedures, or diagnoses; may also collect other specimens, such as urine, sputum, or throat swabs.
• Prepare samples for testing and storage, and label them for analysis.
• Verify the patient's records, enter data into the system, and prepare specimens for laboratory analysis.
• Prepare, maintain, and dispose of medical instruments, such as needles, test tubes, blood vials, and study supplies for visits. Also responsible for maintaining a clean and sanitary work environment.
• Explain procedures to patients to help them feel more comfortable and remain calm.
• May conduct intake interviews, take vital signs, and perform clerical work.
• Assist in the creation of laboratory documents (harvest logs, etc.).
• Pack and properly label all study materials for storage or return to sponsor upon study close‑out.
• Comply with regulation and protocols, attend meetings, trainings, and work cooperatively with the research team and co‑workers.
• Support and ensure strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), Cen Exel standard operating procedures, site working practices, protocol and company guidelines and policies.
• Assume other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered all inclusive.

Education/Experience/

Skills:

• Must be able to effectively communicate verbally and in writing.
• Minimum:
  High School graduate or GED equivalency.
• Vital checks and EKG experience.
• Motivated to work consistently in a fast‑paced and rapidly changing environment.

Working Conditions

• Indoor, clinic environment.
• Essential physical requirements include sitting, typing, standing, and walking.
• Lightly active position, occasional lifting of up to 20 pounds.
• Reporting to work, as scheduled, is essential.
• This is an on‑site work arrangement.

Cen Exel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.