Current jobs related to Clinical Study Sample Processor I - San Diego - PROMETHEUS LABORATORIES INC
-
Clinical Research Nurse I
4 weeks ago
San Antonio, Texas, United States ICON Clinical Research Full timeJob Title: Clinical Research Nurse IICON Clinical Research is seeking a highly skilled and motivated Clinical Research Nurse I to join our team. As a Clinical Research Nurse I, you will play a critical role in supporting the execution of clinical trials, ensuring adherence to protocol requirements, and providing compassionate patient care throughout the...
-
Clinical Research Nurse I
4 weeks ago
San Antonio, Texas, United States ICON Clinical Research Full timeClinical Research Nurse I Job DescriptionICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Job SummaryWe are currently seeking a PRN (as needed)...
-
Study Start-Up Specialist
1 week ago
San Diego, California, United States Vanguard Clinical Full timeJob SummaryVanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA. Our mission is to bring innovation to clinical trial execution through passion, transparency, co-active communication, and integrity, to facilitate the successful development of life-changing medicines and therapies.We are experts in clinical trial...
-
Clinical Research Associate I, PER DIEM
2 months ago
SAN DIEGO, United States CEDARS-SINAI Full timeJob DescriptionPrimary Duties and ResponsibilitiesThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case...
-
Clinical Research Associate I, PER DIEM
2 months ago
SAN DIEGO, United States CEDARS-SINAI Full timeJob Description Primary Duties and ResponsibilitiesThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing...
-
Clinical Study Manager
7 days ago
San Diego, California, United States Modular Medical Inc Full timeJob Title: Clinical Study ManagerModular Medical Inc is seeking a highly skilled Clinical Study Manager to oversee the planning and execution of clinical studies. The ideal candidate will have a strong background in clinical research and experience managing medical device and/or combination products clinical research studies.Key Responsibilities:Develop and...
-
Director of Clinical Operations
5 months ago
San Antonio, United States Worldwide Clinical Trials Full timeWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...
-
Director of Clinical Operations
4 weeks ago
San Antonio, United States Worldwide Clinical Trials Full timeWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...
-
Director of Clinical Operations
2 months ago
san antonio, United States Worldwide Clinical Trials Full timeWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...
-
Clinical Research Associate I
3 months ago
San Diego, United States CEDARS-SINAI Full timeJob DescriptionCome join our team!The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms,...
-
Study Director
4 weeks ago
San Diego, California, United States Simply Biotech Full timeJob Title: Study DirectorSimply Biotech is seeking an experienced Study Director to join our Research and Development team. As a key member of our team, you will be responsible for overseeing the colony management of small and large animals, driving Vivarium Operations, and ensuring the successful execution of research studies.Responsibilities:Oversee all...
-
Clinical Research Coordinator I
3 days ago
San Diego, California, United States Cedars-Sinai Full timeAt Cedars-Sinai, we are seeking a highly skilled Clinical Research Coordinator I to join our team. This role is responsible for providing study coordination, screening potential patients for protocol eligibility, and presenting non-medical trial concepts and details.Independent study coordination, including screening of potential patients for protocol...
-
Clinical Operations Manager
2 weeks ago
San Diego, California, United States Vanguard Clinical Full timeJob Title: Clinical Operations ManagerVanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA, USA. Our mission is to bring innovation to clinical trial execution through passion, transparency, co-active communication, and integrity, to facilitate the successful development of life-changing medicines and therapies.Job...
-
Clinical Operations Manager
7 days ago
San Diego, California, United States Vanguard Clinical Full timeJob SummaryVanguard Clinical is seeking a highly skilled Clinical Operations Manager to oversee the execution and communication of clinical research studies and operations. The ideal candidate will have a strong background in clinical trial management, with experience in managing both projects and direct reports. This is an exciting opportunity to join a...
-
Clinical Phlebotomy Specialist
2 weeks ago
San Diego, California, United States ALLIANCE CLINICAL LLC Full timeJob SummaryThe Clinical Phlebotomy Specialist will perform phlebotomy on research clinic patients using established laboratory procedures under the direction and ongoing supervision of the Clinical Operations Manager and the Principal Investigator.Key Responsibilities:Comply with all company policies, procedures, and conduct.Strictly adhere to...
-
Clinical Research Nurse
2 weeks ago
San Antonio, Texas, United States ICON Clinical Research Full timeClinical Research Nurse I (PRN) Job DescriptionICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.We are currently seeking a PRN (as needed) Clinical...
-
Quality Control Scientist I
2 weeks ago
San Diego, California, United States Truvian Sciences Full timeAbout Truvian SciencesWe are a pioneering healthcare company at the intersection of diagnostics and consumer tech. Our mission is to revolutionize blood testing by developing an automated benchtop diagnostic system that provides lab-accurate results in 30 minutes or less. This innovative approach is set to transform the healthcare industry by making blood...
-
Toxicologist Principal Study Director
20 hours ago
San Diego, United States W3Global Inc Full timeJob DescriptionJob DescriptionSummaryUnder the guidance of the Director, In Vivo Pharmacology, the Principal Scientist will be responsible for the comprehensive design, planning, and execution of in vivo studies. The Principal Scientist will be responsible for the design, conduct, execution and reporting of pre-clinical studies and other research projects,...
-
San Diego, California, United States CEDARS-SINAI Full timeJob DescriptionThe Clinical Research Associate I plays a crucial role in the coordination and implementation of studies, working closely with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse. Key responsibilities include evaluating and abstracting research data, ensuring compliance with protocol and research objectives, and...
-
Lecturer - Environmental Studies
2 weeks ago
San Diego, California, United States UC San Diego Full timeJob Title:Lecturer - Environmental StudiesJob Summary:We are seeking a highly qualified Lecturer in Environmental Studies to join our faculty at the University of California, San Diego. The successful candidate will have a strong background in Environmental Studies, Ecology, or a related field, and will be able to teach a diverse range of courses, including...
Clinical Study Sample Processor I
2 months ago
SUMMARY
Responsible for Saturday receipt and handling of commercial laboratory specimen for commercial testing. Responsible for Tuesday-Friday receipt, handling and processing of clinical study samples received by our Corporate Biobank. This can be for single or batch shipments as part of; company sponsored clinical studies, research collaborations, or pharma partners’ clinical studies. In addition, supports sample request activities for clinical study samples (e.g. pull aliquots from our controlled inventory, prepping aliquots for CLIA testing).
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: Other duties as assigned.
- Management of daily receipt, handling and storage of prospective (single) clinical study samples (either company sponsored, collaborations, or pharma studies), including the archiving of the associated documents, and data entry into the LIMS system for e-tracking.
- Receipt, handling and storage of periodic retrospective (batch) sample shipments from clinical studies (either company sponsored, collaborations, or pharma studies), including verification of vial information against E-manifest, labeling of vials, and filing of paperwork.
- Prepare aliquots for testing in commercial (LIMS readiness), or research laboratories, this might include, but is not limited to create/transfer aliquots containing whole blood, serum, plasma, PBMC, tissue and feces.
- Insure that “chain-of-custody” for all corporate biobank procured samples is maintained upon receipt (GCP).
- De-identify samples received with protective health information (PHI) or those that can be linked to personal identifiable information (PII).
- Generate aliquot inventory of legacy cohorts identified while; using a specific software template, working on dry ice, and limit frequency of freezer access while keeping the specimen frozen at all times.
- Quarantine unknown shipments and those shipments not associated with an executed legal agreement
- Use handheld and plate barcode scanners and associated software.
- Receipt of shipments with visible biohazardous material on outside of the shipper, including the proper handling and disposal of such shipment.
- Responds to freezer alarms and coordinate transfer of contents as required
- Coordinates PM and refrigerator/freezer cleaning with Metrology
- Accession commercial test orders (on Saturday)
- Responsible for initiating Corporate Biobank deviations for sample & shipment conditions deviating for the standard operating procedures.
- Work closely with Corporate Biobank Manager to manage existing inventory, including but not limited to creating inventory of legacy collections, review available capacity for efficient use of storage space, and prepare freezers for Metrology for PM and temperate (re-)validations activities.
- Maintaining an accurate inventory in LIMS system of physical inventory in stand-alone controlled freezers.
- Present during laboratory operating working hours: Tuesday – Saturday
- Required to follow all safety procedures, policies and precautions.
- Must be an excellent team player, communicator and proactive in addressing upcoming issues regarding time lines, workload, or any other workflow related issues.
QUALIFICATIONS
An individual must be able to perform the essential duties satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE
Position generally requires a high school diploma or general education degree (GED) and 2+ years related experience. Preferred is a Bachelors degree. Must have the ability to work in a team structure and to plan, organize and prioritize work. Data entry experience strongly preferred. Experience working in a CLIA/CAP, GCP or GMP/FDA regulated environment preferred. Eye for detail and comfort with different software systems is critical (e.g. Excel, Access, Word, VisionMate), where experience working with a LIMS (StarLIMS, LabVantage) is preferred. Ability to effectively recognize and comfortably switch between (standard operating) procedures on a daily basis. Ability to effectively follow instructions of multiple standard operating procedures on different laboratory workflows is required. Strong laboratory skills (including use of pipets, centrifuges and barcode scanners) and communication skills are required. Working knowledge of clinical science, translational medicine, and/or genetic testing is beneficial.
LANGUAGE SKILLS
Ability to read and comply with all applicable laboratory regulated guidelines. Ability to write reports, and procedure manuals. Ability to effectively work cross functionally and build strong working relationships with others.
MATHEMATICAL SKILLS
Ability to work with mathematical concepts up to probability and statistical inference. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Ability to use Excel to match values.
REASONING ABILITY
Ability to define problems, identify root causes, collect data, establish facts and draw reasonable conclusions. Ability to interpret a variety of technical instruction in diagram or table form. Ability to understand and comply with all applicable laboratory regulated guidelines.
CERTIFICATES, LICENSES, REGISTRATIONS
None.
PHYSICAL DEMANDS
The 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.
While performing the duties of this job, the employee is regularly required to sit and talk or hear. Depending on the task at hand sitting might include looking downwards for extended periods of time. The employee frequently is required to use hands to finger, handle, or feel and work with dry ice. The employee is occasionally required to stand, walk, and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, potentially infectious bodily fluids, toxic or caustic chemicals, and extreme cold. The noise level in the work environment is moderate.
The statements herein are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.
All qualified applicants are considered for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, veteran status or other protected class.