Laboratory Technician Phlebotomist

Job description

Job Description Job Description 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

Demonstrated organizational 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

Competencies: 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.

Worksite address

dallas, TX, 75231, US

Who can apply

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