Laboratory Technician

Pinnacle Clinical Research; Austin (TX); Presencial; USD 25.000 - 36.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

401k

Medical, dental, vision, long-term and

Disability insurance (LTD/STD)

FSA

Life insurance

3 weeks paid time off

14 paid company holidays

Scrub voucher

And more!

Descripción de la vacante

Pinnacle Clinical Research in Austin, TX is seeking a Laboratory Technician (Phlebotomist) to run daily lab operations, collect blood and other specimens, and ensure proper processing and shipping according to study protocols. You will maintain documentation, manage supplies, and collaborate with the PCR team to support clinical trials while adhering to safety and quality standards.

Ideal candidates have basic phlebotomy experience, strong communication, and the ability to multitask in a

Formación

• High school diploma or equivalent is required.
• Certified in phlebotomy preferred with at least 1 year of experience.
• Must be able to follow study protocols and safety guidelines.
• Strong communication and multitasking skills.

Responsabilidades

• Perform lab tests, collect subject specimens, and process samples according to the study lab manual.
• Daily phlebotomy and specimen processing with universal precautions.
• Use appropriate needles and techniques to obtain quality specimens with minimal discomfort.
• Store, track, and ship samples to central/local labs per study procedures.
• Maintain lab inventory and ensure no expired kits; document temperature logs.
• Upload requisitions into CRIO and route to CRC or Research Assistant daily.
• Maintain equipment records and daily work logs; ensure compliance with SOPs.

Conocimientos

Phlebotomy

Lab operations

Specimen processing

Communication

Documentation

CRIO/CTMS familiarity

BLS training

Medical terminology

Educación

High school diploma

Phlebotomy certification

Herramientas

Microsoft Office

Descripción del empleo

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Laboratory Technician (Phlebotomist)

Clinical Operations ATX Full Time Austin, TX, US

2 days ago Requisition ID: 1117

Summary: The Laboratory Technician will be responsible for running the day-to-day operations of the lab. They will aid in research-related activities and clinical research, including collecting blood, urine/stool or tissue samples, and processing/shipping biological samples, as well as maintaining all laboratory documentation and supplies. This person must have a minimum of 12 months of laboratory experience in a healthcare setting and be able to understand laboratory priorities and establish a workflow to complete all required activities in a timely manner.

The Lab Technician must be organized, excel at multitasking, detail-oriented, an excellent communicator, and be able to provide high-quality patient care. This person will collaborate very closely with other members of the PCR team and therefore must be highly collaborative, goal-oriented, flexible, and communicative. An ideal candidate will be responsive, self-motivated, and a team player. This role reports directly to the Laboratory Manager or the site Clinical Operations Manager.

Duties and Responsibilities:

Perform lab tests, collect subject specimens, and process samples according to the corresponding study lab manual

Responsible for daily phlebotomy (venipuncture, IV catheter, or capillary collections) and specimen processing, and biological sample shipping using universal precautions

Uses proper tools such as an appropriate needle gauge and type of needle (straight needle, butterfly, or IV catheter) and judgment to obtain optimum specimens while minimizing discomfort and hazards for the patient

Collect, organize, store, and ship samples in accordance with quality control and all safety and other requirements to ensure the safety of personnel and integrity of the sample

Ship processed specimens to the central and/or local lab in a timely manner and according to study lab manuals

Track inventory of lab kits from the central lab and re-order as needed. Ensure there are no expired lab kits on the premises

Track inventory of lab supplies and shipping containers and re-order as needed

Maintain a clean and sanitary laboratory area, storage area, and lab restroom always. Clean and maintain lab equipment, including alerting the Lab Manager or Clinical Research Project Manager when recalibration of equipment is needed

Facilitating or advising the lab manager/project manager for biohazard pickups

Complete and upload lab requisitions into Clinical Research IO (CRIO) and subject folders daily, as well as file the physical copies

Distribute lab requisitions to the appropriate CRC or Research Assistant daily for filing

Receive and process deliveries for the lab (e.g., upload temperature logs into the share drive, ensure product quantity matches shipping manifest, etc.).

Maintain equipment records, temperature logs, inventory trackers, PK logs, and daily work logs in a timely manner

Complete the required data entry daily and ensure inventory is tracked in a timely manner

Retrieve subject specimens from local vendor locations if applicable (i.e., liver biopsy tissue)

Communicates pertinent medical history information to the appropriate coordinating staff

Exercises judgement within the allowable limits defined within clinical trials protocols, standard operating procedures under the direction of the study Investigator and supervisor

Interacts with internal and external personnel to include, but not limited to, physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel and clinical trial patients

Duties, responsibilities, and activities may change, or new ones may be assigned at any time.

Education/Experience:

• A high school diploma or equivalent is required
• Certified in phlebotomy preferred with at least 1 year of experience

Knowledge, Skills, and Other Abilities:

• Strong verbal and written communication skills
• Must complete CITI and GCP training before interacting with participants and must recertify every 3 years
• Must complete IATA Dangerous Goods Training and recertify every 2 years
• Must complete basic life support (BLS) training (training will be provided by PCR)
• Proficient in all Microsoft Office applications and Clinical Research IO (CRIO) or equivalent CTMS
• Valid driver's license with maintenance of a safe driving record, and an automobile that is insured in accordance with the state
• Flexibility with work schedule- early shifts, late shifts, weekend shifts
• Demonstratedorganizational skills and outstanding time management, including keen attention to detail, with the ability to track multiple projects at one time
• Intermediate-level knowledge of medical terminology
• Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission
• Comply with the company policies, code of ethics, and guiding values always
• Proficient in English and Spanish preferred
• Must be able to effectively communicate with all levels of internal and external contacts
• Ability to work independently and multitask in a fast-paced team environment
• Strong people skills, including the ability to interact with individuals from diverse backgrounds and to oversee confidential matters and sensitive information with discretion and judgment
• Strong organization and time management skills with an elevated level of attention to detail
• Ability to quickly learn and process information
• Must be able to work independently and collaborate with a team
• Energetic self-starter, results-oriented, and the ability to work effectively in an entrepreneurial environment
• Ability to interpret clinical research protocols and lab manuals
• Strong problem-solving and decision-making skills, particularly when under pressure
• Proactive in identifying, addressing, and solving issues in real time

Work Environment and Physical Demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Work is performed in an office/laboratory and/or a clinical environment.
• Exposure to biological fluids and/or bloodborne pathogens.
• Personal protective equipment is required, such as protective eyewear, garments, and gloves.
• Occasional travel may be required, domestic and/or international.
• Ability to work in an upright and/or stationary position for 6-10 hours per day.
• Frequent mobility required.
• Occasional squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment, with a maximum lift of 20-50 lbs.

Perks of working at Summit Pinnacle Clinical Research:

• 401k
• Medical, dental, vision, long-term disability, short-term disability, FSA, and life insurance
• 3 weeks of paid time off
• 14 paid company holidays
• Scrub voucher (specific positions apply)
• And more!

Summit Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.