Clinical Laboratory Coordinator

• Is assigned to key studies/protocol(s) as laboratory lead

• Is responsible for allocation of supplies for assigned protocol(s)

• Is responsible for training of support laboratory technicians per assigned protocol(s)

• Conducts quality checks on trained laboratory technicians (e.g. processing, storage, documentation)

• Attends site initiation meetings (SIV) as a representative of the lab

• Possesses detailed lab knowledge for the assigned study protocol(s)

• Responsible for clarifying any lab discrepancies with sponsor.

• Creates requisitions for “Dummy Panels” for assigned protocol(s), QAs results and forwards results to sponsor.

• Is responsible for lab collection, processing, and transport/shipment of safety labs according to clinical study protocol.

• QAs tube/container labels before and after specimen collection.

• Is responsible for setting up any external vendor needs for the assigned protocol(s).

• Receives and inventories lab supplies for the assigned protocol(s).

• Creates all lab source documents for the assigned protocol(s) (e.g. PK log, Urine log, PK instruction posters, etc.)

• Responsible to inventory, ship, and track all protocol specimens to the sponsor/vendor laboratory.

• Contacts sponsor to confirm arrival of specimen shipments.

• Closes communication with protocol assigned Clinical Research Coordinator (CRC) and helps problem solve day to day lab issues with CRC.

• Liaises with hospital lab as needed.

• Attends Early Phase meetings (e.g. Lab, CRC, Staff) as appropriate.

• Assists in protocol feasibility review for the laboratory.

• Maintains and updates knowledge for Clinical Operating Guidelines and their proper application.

• All other duties as assigned.

• Meticulous attention to detail

• Strong interpersonal, written/verbal communication and organizational skills

• Strong leadership skills

• Ability to effectively manage time and multi-task

• Ability to function well in a team environment

• Computer proficiency required

• Flexible schedule

• Local travel may be required: valid California Driver’s License and/or reliable transportation

• Ability to lift up to thirty (30) poundsQualifications• BA or BS in related science field preferred

• Valid Phlebotomy Certification and/or California State Licensure preferred

• Valid CPR Certification

• 2-3 years of related lab bench experience in an analytical or clinical research laboratory preferredEEO DisclaimerPAREXEL complies with all applicable federal, state, and local laws prohibiting discrimination in employment. All qualified applicants will receive consideration for employment without regard to gender, age, race, color, religious creed, marital status, sexual orientation, national origin, ethnicity, ancestry, citizenship, genetic information, disability, protected veteran status or any other characteristic protected by applicable federal, state or local law.