Page Mechanical Group, Inc.
Pharmacokinetic (PK) Lab Technician - Los Angeles, CA
Page Mechanical Group, Inc., Los Angeles, California, United States, 90079
The START Center for Cancer Research ("START") is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.
Pharmacokinetic (PK) Lab Technician We are hiring a
Pharmacokinetic (PK) Lab Technician
in our Los Angeles, CA (10700 Santa Monica, Suite 310, Los Angeles, CA) location who will support the investigation team in adherence to phase 1 research protocols within the Standard Operating Procedures of the department. Under general supervision, this position performs laboratory receiving, processing, handling, storage and shipping procedures, equipment maintenance and inventory control within the Pharmacokinetic Department.
The hourly rate for this role is $27 – $32/hour. Your compensation may vary based on your unique qualifications, experience, and market factors.
Essential Responsibilities
Ensure compliance with all applicable Federal, State and local laws and regulations as they apply to biological sample processing, handling, and shipping.
Receive, process, handle, store, and ship biospecimens per study specifications.
Prepare research sample collection supplies per specific study specifications.
Adhere to the company SOP and GLPs.
Recognize inconsistencies in sample collection data and take appropriate corrective action as needed. Contact Nurse immediately to have situation corrected before patient leaves the building.
Record data in electronic data systems in compliance with SOPs and GLP.
Process and ship tissue specimens according to protocol requirements. Coordinate with other healthcare providers to receive patient tissue. Prepare tissue specimens as needed per study protocol.
Perform administrative functions associated with the Pharmacokinetic Department, to include but not limited to work tally records, scanning internal and study specific forms, filing, and sample management documentation.
Complete study forms to include but not limited to shipping logs, shipping documentation, sample requisition forms, flow sheets, and sample manifests.
Contribute to study specific and departmental inventory control and re-supply of reagents and supplies as needed. Replenish lab supplies daily.
Sanitize laboratory equipment daily, weekly, monthly, and yearly.
Perform and record daily/weekly/annual maintenance of equipment.
Participate in on-call rotation for emergency response for drug and specimen storage. Participate in on-call rotation for emergency management.
Education & Experience
High School Diploma.
General knowledge of medical terminology.
High attention to detail and strong organizational skills.
Excellent written and verbal communication skills.
Ability to work well independently.
Organizational skills to troubleshoot unplanned situations while still meeting established deadlines.
Proficient level of experience with Microsoft Office and the ability to learn new software.
Must maintain punctuality, good attendance and be flexible to work hours to accommodate clinic patient schedule.
Preferred Education and Experience
Associate or bachelor’s degree in a chemical, physical, biological or clinical laboratory science or medical technology.
Experience in a laboratory setting, with a solid understanding of laboratory techniques and safety protocols.
Experience in data management.
Experience in logistics and operations.
Experience with electronic medical record program(s) and laboratory information systems.
Physical & Travel Requirements
Able to perform manual tasks that require the use of fine muscle motor skills.
Able to lift 40 pounds.
Able to stand and / or sit for prolonged periods.
Able to freely bend/stretch. Able to access, input and retrieve information from computer.
Best-in-Class Benefits and Perks
Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided (if applicable)
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
More about The START Center for Cancer Research Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
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START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.
Pharmacokinetic (PK) Lab Technician We are hiring a
Pharmacokinetic (PK) Lab Technician
in our Los Angeles, CA (10700 Santa Monica, Suite 310, Los Angeles, CA) location who will support the investigation team in adherence to phase 1 research protocols within the Standard Operating Procedures of the department. Under general supervision, this position performs laboratory receiving, processing, handling, storage and shipping procedures, equipment maintenance and inventory control within the Pharmacokinetic Department.
The hourly rate for this role is $27 – $32/hour. Your compensation may vary based on your unique qualifications, experience, and market factors.
Essential Responsibilities
Ensure compliance with all applicable Federal, State and local laws and regulations as they apply to biological sample processing, handling, and shipping.
Receive, process, handle, store, and ship biospecimens per study specifications.
Prepare research sample collection supplies per specific study specifications.
Adhere to the company SOP and GLPs.
Recognize inconsistencies in sample collection data and take appropriate corrective action as needed. Contact Nurse immediately to have situation corrected before patient leaves the building.
Record data in electronic data systems in compliance with SOPs and GLP.
Process and ship tissue specimens according to protocol requirements. Coordinate with other healthcare providers to receive patient tissue. Prepare tissue specimens as needed per study protocol.
Perform administrative functions associated with the Pharmacokinetic Department, to include but not limited to work tally records, scanning internal and study specific forms, filing, and sample management documentation.
Complete study forms to include but not limited to shipping logs, shipping documentation, sample requisition forms, flow sheets, and sample manifests.
Contribute to study specific and departmental inventory control and re-supply of reagents and supplies as needed. Replenish lab supplies daily.
Sanitize laboratory equipment daily, weekly, monthly, and yearly.
Perform and record daily/weekly/annual maintenance of equipment.
Participate in on-call rotation for emergency response for drug and specimen storage. Participate in on-call rotation for emergency management.
Education & Experience
High School Diploma.
General knowledge of medical terminology.
High attention to detail and strong organizational skills.
Excellent written and verbal communication skills.
Ability to work well independently.
Organizational skills to troubleshoot unplanned situations while still meeting established deadlines.
Proficient level of experience with Microsoft Office and the ability to learn new software.
Must maintain punctuality, good attendance and be flexible to work hours to accommodate clinic patient schedule.
Preferred Education and Experience
Associate or bachelor’s degree in a chemical, physical, biological or clinical laboratory science or medical technology.
Experience in a laboratory setting, with a solid understanding of laboratory techniques and safety protocols.
Experience in data management.
Experience in logistics and operations.
Experience with electronic medical record program(s) and laboratory information systems.
Physical & Travel Requirements
Able to perform manual tasks that require the use of fine muscle motor skills.
Able to lift 40 pounds.
Able to stand and / or sit for prolonged periods.
Able to freely bend/stretch. Able to access, input and retrieve information from computer.
Best-in-Class Benefits and Perks
Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided (if applicable)
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
More about The START Center for Cancer Research Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
#J-18808-Ljbffr