Laboratory Technician

Duties and Responsibilities

• Perform lab tests, collect subject specimens, and process samples according to 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 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 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
• Facilitate or advise 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 appropriate CRC or Research Assistant daily for filing
• Receive and process deliveries for the lab (e.g. upload temperature logs into 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 appropriate coordinating staff
• Exercises judgement within the allowable limits defined within clinical trials protocols, standard operating procedures under the direction from 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

Education/Experience

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

Education/Experience

• Knowledge, Skills, and Other Abilities:
• Strong verbal and written communication skills
• Must complete CITI and GCP training before interacting with participants and must re-certify every 3 years
• Must complete IATA Dangerous Goods Training and re-certify 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
• A valid driver's license with maintenance of 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 multi-task 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
• The 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
• Proactive at identifying, addressing, and solving issues in real time
• Strong problem-solving and decision-making skills, particularly when under pressure

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 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 moves) objects including medical equipment with a maximum lift of 20-50 lbs.