Frontline National is seeking qualified individuals to work as Phlebotomists to support RTI International in implementing a research project in Newburgh, New York. Please apply online or call our office directly at 513-528-7823 to learn more about this great opportunity!
For the study, recruited research participants will be scheduled for appointments at a local study office in Newburgh, New York. At the office, participants will meet with a Phlebotomist who will collect measurements such as height, weight, waist circumference, and blood pressure, and a blood sample. Participants will also complete a survey about their health, and minor participants will complete a neuro-behavioral assessment. Study office staff will also receive participant urine samples, process blood samples into serum aliquots, and ship the blood, serum, and urine samples to off-site labs for analysis. The team will be overseen by an on-site office manager or team lead.
Daily responsibilities include, but are not limited to:
- Using interpersonal and verbal communication skills to communicate effectively with study office leadership and participants.
- Verifying participant identities and looking up their Participant IDs in the project system to begin their study office activities.
- Collecting and documenting COVID-19 screening questions (when needed) and temperature accurately.
- Collecting confidential information and administer Informed Consent Forms.
- Collecting and documenting anthropometric measurements and blood pressure accurately.
- Performing venipuncture and/or capillary specimens from study participants according to established protocols, maintaining aseptic techniques.
- Performing proper and accurate sample management, including collection, identification, transport, and processing of participants’ biological samples.
- Providing a clear explanation of study procedures to participants and their family.
- Reporting any subject complaints of adverse events.
- Completing data collection forms as required for the study in a timely manner.
- Entering information in computer databases for the study in a timely manner.
- Providing information on the data collected to appropriate members of the project team as directed.
- Receiving, processing, and temporarily storing biospecimens in freezers and refrigerators.
- Preparing shipments and shipping biospecimen samples according to study protocols.
- Tracking biological samples using biospecimen management software.
- Maintaining inventory of biospecimen collection and storage materials.
- Following laboratory safety rules and procedures.
- Cleaning and sanitizing the laboratory, biospecimen processing equipment, and storage freezers and refrigerators.
- Managing medical and hazardous waste.
- Working comfortably on a study-provided computer or tablet.
- Following protocol and manual of procedures processes.
- Managing and operating equipment safely and correctly.
- Maintaining cleanliness of medical equipment used.
- Maintaining cleanliness of study office areas as assigned.
- Maintaining participant confidentiality.
- Complying with all COVID-19–related safety requirements.
- May be asked to assist with study office set-up prior to data collection launch.
- Other duties as required.
- Successfully completed an accredited phlebotomy program
- One (1) year of phlebotomy experience preferred.
- Pediatric experience preferred.
- Basic laboratory and troubleshooting skills and trained in aseptic technique.
- Effective communication skills through speech and listening and have fluency in English through reading, writing, and speaking.
- Basic computer skills.
- Able to keep project information confidential.
- Good attention to detail, excellent documentation skills, and ability to work well in a group environment.
- Ability to report to work on time as scheduled.
- Ability to comply with all study ethics practices.
- Strong written and verbal communication skills.
- Must be at least 18 years old at the time of employment.
- National Background Investigation
- Must be authorized to work in the U.S.
- Must have a valid driver’s license and reliable transportation to and from study office.
License/Certification and Training:
- Certification by one or more of the following is preferred: American Certification Agency for Healthcare Professionals (ACA), American Medical Technologists (AMT), The National Center for Competency Testing (NCCT/MMCI), The American Society for Clinical Pathology (ASCP), American Medical Certification Association (AMCA), or National Healthcare Association (NHA).
- Current certification in CPR and First Aid from an accredited institution required.
- Attend and successfully complete up to 40 hours of project training.
- Staff must also complete the requirements of an 8-hour research with human subjects training.
- Personal Protective Equipment (PPE) will be provided as well as training regarding the proper use and disposal of PPE per Center for Disease Control (CDC) guidelines.
- Hazards: Potential exposure to blood-borne pathogens.
- As part of preventative measures to protect staff and participants, all staff are encouraged to get vaccinated against COVID-19 prior to beginning work.
- Available to work, on average, three to five 5-hour shifts per week from approximately September 2021 through March 2022. Study office hours will vary by month, but shifts will primarily start at 6:30 AM and end between 12:00 PM and 2:00 PM Monday through Saturday and 3:00 PM through 8:00 PM once or twice a month. The Office Manager will coordinate shift schedules.
- Availability for entire training and data collection period.