Natera jobs

L3 Technical Support CEBU CITY, PHL posted: Posted 16 Days Ago

Histology Lab Operator II San Carlos, CA POSITION SUMMARY: The Histology Lab Operator II is a member of the Histopathy Department responsible for assisting HT/HTLs in analyzing specimens and maintaining equipment in good condition. PRIMARY RESPONSIBILITIES: • Assists certified/licensed personnel in clinical patient testing in accordance with the SOP • Perform histological preparations for the tissue whole exome sequencing laboratory with little to no errors • Duties may include but not limited to: preparation of tissues, stained slides, macrodissection and supporting workflow tasks • Sets up equipment and assists with automated lab procedures, as applicable • Assist and complete daily tasks • Maintains equipment and instruments in good operating condition • Maintain sufficient inventory of material, supplies, and equipment in the laboratory for the performance of duties • Documents information accurately and in accordance with Good Documentation Practices (GDP) • Provides Guidance for new team members • Train on specialized instructions for instruments/protocols (super users) • Identifies and escalates stuck cases and unresolved issues • Performs other duties as assigned QUALIFICATIONS: • A minimum of 2+ years related experience • An associate's, or higher, degree in a histotechnician program OR An associate's degree, or higher, in one of the chemical or biological sciences AND one year of experience and/or training in histology within the past 5 years OR - completion of a course of training of at least nine months in a histotechnician program OR A bachelor's, or higher, degree in one of the chemical or biological sciences, including a

Senior Quality Clinical Data Abstractor US Remote POSITION SUMMARY: Perform high-quality medical record abstraction by combining proficient-level experiences in data management and software with medical terminology, medical coding, information encoding, and analytical capabilities. Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting. PRIMARY RESPONSIBILITIES: - Data Abstraction: Accurately review, interpret, and abstract clinical patient data from various electronic health record (EHR) systems, paper charts, and other source documents in accordance with defined project or research protocols, clinical, data, and technical specifications, and dictionaries. - Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data points from unstructured text to standardized machine readable data in one common database schema. - Electronic Data Capture (EDC): Utilize specialized data management software (e.g., REDCap, registries, and custom built EDC systems) to enter, track, and maintain the integrity of clinical data encoded into queryable databases. - Technical Support: Aid cross-functional teams in translating clinical and data abstraction and encoding requirements. Support prompt engineering and design for all AI and LLM initiatives. - Data Management: Apply and support establishing program specific clinical data management best practices (CGDMP) and good clinical practice (GCP) during the abstraction and encoding process resulting in accurate, legible, contemporaneous, original, attributable, complete and consistent for end-to-end ETL workflows. - Quality Assurance and Control: Apply industry standard best practices for utilizing real-world data for research, quality monitoring, and regulatory reporting using

Supervisor, Histology San Carlos, CA POSITION SUMMARY: As the Histotechnologist Supervisor you will oversee the activities of the lab and Signatera team that is cutting, staining and preparing tissue samples for the pathologist view. The individual is responsible for supervising and participating in operations of the histology lab. PRIMARY RESPONSIBILITIES: - In this position, you will work in a fast paced, customer focused, and challenging environment - Supervise the day-to-day operations of the Histology department - Ensure laboratory tests are accurately performed and results are reported in a timely manner - Directly supervise, train, and mentor laboratory personnel of the department - Monitor daily workflow in the lab and schedule adequate assay coverage - Responsible for ensuring all shifts in the department are properly staffed - Research and resolve any production errors while escalating when necessary - Engage in continuous process and service level improvements - Ensure all equipment is being properly maintained through Quality Control - Prepare and maintain Quality Assurance records and documents - Evaluate new process improvements and make appropriate recommendations - Meet regularly with direct reports to provide coaching and feedback for their development - Perform bench work as needed and maintain proficiency/competency in technical operations - Ensure all work is in accordance with state and Federal regulations - Responsible for administering and managing policies and procedures - Process and maintain payroll and personnel files - Perform administrative duties as needed Qualifications - Bachelor's Degree required - Active ASCP Board of Certification, HT(ASCP), HLT(ASCP) - 4+

Senior Lab Automation Engineer Austin, TX POSITION SUMMARY: The Senior Lab Automation Engineer is an experienced engineer with expertise in the development and implementation of complex laboratory automation and integrated systems. They can work independently to conceptualize, design, develop and implment automated solutions for robust, reliable performance of NGS assays. This development includes standalone instruments and integrated systems. They can work together with cross-fucntional teams of scientists, engineers, and software engineers to deliver these automated platforms. In addition, they can provide high-level support for any of the processes they develop - both at an instrument and an assay results level. This engineer can perform their role independently, but will most often be a part of a larger overall development and will have to be capable of working well in a team environment. They lead by example and contribute to the team beyond their day to day duties. QUALIFICATIONS: - Bachelor's degree in Biomedical Engineering, closely related scientific field or equivalent. - 4+ years of experience in laboratory automation engineering. - Technical proficiency and experience in automation and systems development and integration in the life sciences industry; especially with robotics and liquid handling systems. - Background in NGS laboratories is a plus, as is background in clinical laboratories. - Experience in software programming and data handling (including database work) is a plus. - Strong attention to detail and organizational skills required. - Excellent problem solving skills. - Strong written and verbal communication skills are required. - Flexibility to support several simultaneous

MLS Data Reviewer I US Remote POSITION SUMMARY: The Medical Laboratory Scientist I, Data Reviewer is a member of the Operations Department to review and analyze clinical test results. This individual collaborates with a team of CLS and laboratory personnel to maintain accurate records of test results and patient information and perform any troubleshooting as needed. PRIMARY RESPONSIBILITIES: • Review clinical test results of molecular genetic testing received from laboratories for accuracy and translate intoLIMS • Review and analyze raw data files in proper software and resolve routine issues • Verify the proper specimen analyzed for patients and review the test requisition forms to verify the correct tests were performed. • Work within several laboratory information systems to review patient demographics and make corrections as needed • Responsible for understanding most current applicable standard operating procedures • Ensures compliance with all regulatory agency requirements through documentation, audits, and corrective action and follows GLP (good laboratory practice) • Comply with all company and department policies and procedures. This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job • Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training, and security training as soon as possible but not later than the first 30 days of hire • Performs other duties as assigned QUALIFICATIONS: • 0-2-years experience as an ASCP-certified Medical Technologist in a clinical laboratory

Stock Associate, Part Time Flex, Corte Madera - Pottery Barn Kids & Teen Corte Madera, CA, United States Stock Associate, Part Time Flex, Corte Madera - Pottery Barn Kids & Teen Corte Madera, CA, United States JOB DESCRIPTION About the Role Receive shipments & accurately maintain inventory records. Maintain stockroom & off-site locations. Assist sales team in replenishing sales floor after shipment or during recovery periods. You're excited about this opportunity because you will... Exemplify the highest level of customer service standards to internal and external customers Scan shipment as delivered Ticket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor Provide feedback to supervisor regarding inventory levels and damages Organize stockroom by department and categories and stock merchandise on appropriate shelves or in offsite locations Adjust stocking procedures to ensure aisles and exits are clear Ensure that merchandise is safely stored, properly ticketed packaged and logged, and easily located for replenishment Pack and log merchandise as required for customer deliveries Transport merchandise to and from remote stockroom locations and maintain accurate inventory records Ensure that the stockroom is clean, swept, with garbage removed and supplies organized May assist on sales floor during peak times and as assigned Complete tasks listed on daily agenda or as assigned (i.e., maintenance of store, lighting, cleaning) Comply with all company policies and procedures Ensure all appropriate stockroom procedures are followed to minimize loss to the company Why you will love working at Williams-Sonoma, Inc. We're a

Clinical Lab Scientist I San Carlos, CA POSITION SUMMARY: The Clinical Laboratory Scientist analyzes specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: • Verify the proper specimen being analyzed and perform tests that need to be completed • Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors • Responsible for maintaining updated understanding and knowledge of methods performed in the lab • Follows GLP (good laboratory practice): maintain clean and organized work space • Completes training and other deadlines on time. • Go-to person when lead/supervisor is not available • Train on specialized instructions for instruments/protocols (super users) • Recognizes and escalates equipment malfunctions; troubleshoots common errors • Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor • Participates in the updating of departmental standard operating procedures and database to accurately reflect the current practices. • Ensures compliance with all regulatory agency requirements through proper documentation • Performs quality control procedures to ensure accuracy of clinical data (if applicable) • Maintains equipment and instruments in good operating condition • Communicates with team and other departments (including via e-mail) • Provides feedback on day-to-day schedule and tasks to lead/supervisor; offers suggestions/ideas for improvement • Assists teammates in completing daily tasks • Conducts himself/herself in a professional manner; acts as a role model/mentor to others • Adheres to Departmental Expectations • This role works with PHI on a regular basis both in paper and electronic form and have an

Sales Associate, Part Time Flex, Corte Madera - Pottery Barn Kids & Teen Corte Madera, CA, United States Sales Associate, Part Time Flex, Corte Madera - Pottery Barn Kids & Teen Corte Madera, CA, United States JOB DESCRIPTION About the Role As a Sales Associate you provide customers with a unique shopping experience by offering excellent customer service. Utilize effective selling techniques and provide in-depth product knowledge in a fast-paced, specialty retail environment. You're excited about this opportunity because you will... Provide sincere, friendly and energetic customer service by exemplifying World-Class service standards Achieve established sales and contest goals Maintain knowledge of current sales and promotions Assist customers with special services including: gift wrap, gift registry, locating merchandise, catalog orders, special orders, back orders, charge sends, courier deliveries, and furniture orders Utilize effective selling techniques to build multiple sales and increase productivity Demonstrate comprehensive product knowledge, including features and benefits Efficiently and accurately perform register transactions i.e. sales, returns, and exchanges Assist in implementation and maintenance of visual merchandise presentation, signage and lighting Uphold store maintenance and cleanliness standards straighten, clean and help maintain stockroom as needed Process, ticket, and restock merchandise as needed Perform other duties as assigned by management Comply with all Company policies and procedures Why you will love working at Williams-Sonoma, Inc. We're a successful, fast-growing company with an entrepreneurial vibe A technologically and data-driven business Competitive salaries and comprehensive health benefits We're at the forefront of tech and retail, redefining technology for the next generation

Clinical Lab Operator I Austin, TX POSITION SUMMARY: Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: • Assist in testing of patient samples according to standard operating procedure. •Meet expected performance metrics within role as applicable. • Responsible for maintaining updated understanding and knowledge of methods performed in the lab • Provide guidance for new team members. • Follows GLP (good laboratory practice): maintain clean and organized workspace • Completes training and other deadlines on time. • Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory's standard operating procedures • Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor • Communicates with team and other departments on various platforms (including via e-mail) • Provides feedback on day-to-day schedule and tasks to lead/supervisor • Assists teammates in completing daily tasks • Maintains equipment and instruments in good operating condition (such as calibration and expiration date) • Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties. • Participate in Continuous Improvement Projects (TAG, 5S) • Conducts himself/herself in a professional manner • Adheres to Departmental Expectations • This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job • Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later

Floater Phlebotomist - Fairfax, VA - Temp Fairfax, VA Position Summary - Temporary Position location in Fairfax, VA The Floater Phlebotomist/Data Entry Analyst is a dual-role position responsible for providing phlebotomy services across multiple IOPs and performing accurate and timely data entry to support clinical and administrative operations. This role requires excellent organizational skills, attention to detail, the ability to adapt to changing environments and the ability to adhere to a strict schedule. Key Responsibilities Phlebotomy : - Perform blood draws and other specimen collections following standard procedures and protocols. - Ensure the comfort and safety of patients during specimen collection. - Accurately label, document, and process specimens for transport to laboratories. - Maintain compliance with all health and safety regulations, including infection control. - Travel between assigned locations to provide phlebotomy services as needed. - Maintain a clean, organized and fully stocked phlebotomy workspace. Data Entry and Analysis: - Enter patient, specimen, and test information into laboratory information systems (LS) with high accuracy. - Receive, review and enter patient data into laboratory information systems (LIS) with high accuracy. - Review and verify data to ensure completeness and correctness. - Compile, organize, and analyze data for reporting purposes. - Identify and correct data discrepancies or escalate issues a necessary. - Maintain confidentiality and security of patient and organizational data in accordance with HIPAA and other regulations. - Complete data entry in a scheduled, timely manner. - Collaborate with management and internal teams to implement and evaluate improvements. - Understand and

Principal, Pharmacovigilance / Device Vigilance US Remote POSITION SUMMARY: The Principal, Pharmacovigilance / Device Vigilance is a detail-oriented and proactive professional supporting the safety surveillance of In Vitro Diagnostic and Software-driven products across their lifecycle, including clinical studies and post-market activities. This role is responsible for the collection, assessment, reporting, and management of adverse events, product complaints, and safety data for both medicinal products and medical devices, ensuring compliance with global regulatory requirements. The position plays a critical role in ensuring compliance with global regulatory requirements (e.g., FDA, EU IVDR, Japan) and maintaining the highest standards of patient safety and product quality across both laboratory-developed tests and regulated IVD products, including software/algorithm-based components. PRIMARY RESPONSIBILITIES: - Pharmacovigilance (Drug Safety) - Perform case intake, triage, and processing of Individual Case Safety Reports (ICSRs) - Process and evaluate adverse events associated with diagnostic use (e.g., clinical impact of false positives/negatives) - Coordinate medical review and causality assessment of adverse events - Coordinate timely submission of safety reports (e.g., MedWatch, EudraVigilance, CIOMS) - Support aggregate reporting (PSUR/PBRER, DSUR, annual reports) - Maintain and ensure compliance with global PV regulations (FDA, EMA, ICH, etc.) - Contribute to signal detection and risk management activities - IVD Device Vigilance - Review, triage, and assess product complaints and adverse events related to genetic and diagnostic testing, including incorrect, delayed, or misinterpreted results - Evaluate reportability of events under FDA (MDR), EU IVDR vigilance, Japan and other global regulations - Prepare and submit Medical Device Reports (MDRs) and

Corporate Compliance Director US Remote POSITION SUMMARY The Director, Corporate Compliance is an individual contributor role that reports to the Sr. Director of Corporate Compliance and assists in leading projects that support overall Compliance initiatives as designated by the Chief Compliance Officer. The position supports the day-to-day functions of the Compliance department as well as special projects and assessments through data analysis, process improvement, auditing, report development, and policy maintenance. PRIMARY RESPONSIBILITIES - Supports the compliance function by developing and executing high level strategic business objectives that support the growth of key business areas. - Supports the compliance department with execution on key strategic objectives of the business that support both long term and short term goals of the three key business units of the company. - Implements key objectives of the Compliance Department that allows for proactive compliance risk identification. - Develops clear, qualitative and/or quantitative analyses in support of Corporate Compliance programs and initiatives. - Develops innovative, interactive, and informative training on a variety of compliance and privacy topics. - Develops, implements, and monitors key compliance functions and risk areas under direction of Sr. Director of Compliance and the Chief Compliance Officer in accordance with OIG guidance for clinical laboratory compliance programs. - Provides analysis and summary reports on an “ad-hoc”, as well as routine basis at the direction of the Sr. Director of Compliance or the Chief Compliance Officer. - Responsible for maintenance of peripheral databases and trackers that support Corporate Compliance reporting needs. - Supports monitoring

Lead Clinical Lab Scientist San Carlos, CA POSITION SUMMARY: Assists in analyzing specimens and works closely with supervisor to make sure production goals are met. PRIMARY RESPONSIBILITIES: - Verify the proper specimen being analyzed for patients and perform correct tests that need to be completed - Assists the team in day-to-day lab work according to standard operating procedure with little to no errors - Follows GLP (good laboratory practice); reports non-conformity of SOPs to supervisor/manager - Ensures production work is consistently completed in a timely manner. - Ensures all case samples are processed and accounted for - Assists supervisor in completing side projects assigned by the manager - Go to person on the lab floor and when supervisor is not present - Trains new hires with the current lab processes and assists supervisor in training/implementation of new process changes. - Assists supervisor and lab trainer in completing competency for staff. - Train on specialized instructions for instruments/protocols (super users) - Recognizes and escalates equipment malfunctions; troubleshoots most errors - Understands the entire lab process and identifies/troubleshoots issues when they arise. - Ensures new lab changes are implemented properly on the lab floor - Escalates lab issues and team concerns to supervisor and/or manager. Suggests possible solutions. - Escalates any discrepancies of team members' performance to supervisor - Provides feedback during performance evaluations for team members - Meets regularly with the Supervisor - Keeps team morale up and maintains professionalism of team members, including by acting as a role model -

Histotechnologist II Austin, TX POSITION SUMMARY: Performs histological preparations for Signatera Whole Exome/Genome Sequencing PRIMARY RESPONSIBILITIES: • Perform histological preparations for the tissue whole exome/genome sequencing laboratory with little to no errors • Duties may include, but are not limited to: preparation of tissues, stained slides, macrodissection, and supporting workflow tasks • May independently perform testing, reagent, and equipment preparation after completion of training and competency. • Participates in validations • Performs qualifications of reagents • Monitors and performs case management; ensures all cases are processed within department TAT goals and investigates sample processing issues • Actively participate in EH&S initiatives such as safety audits • Participates in updating and creating Standard Operating Procedures • May serve as the general supervisor (Depending on education and years of experience) and perform competencies • Trains staff on department procedures • Participates in Projects and initiatives initiated by the department/external departments • Extensive knowledge in equipment and process troubleshooting • Document all corrective actions taken when test systems deviate from the established performance specifications as needed. Escalates protocol deviation to the lead/supervisor. • Provides general oversight of personnel and the daily operations in the lab. Provides guidance to new team members • Engages with external departments such as Engineering, Biodev, Stats to resolve issues • May work with leaders of the department to streamline processes. QUALIFICATIONS: An associate's, or higher, degree in a histotechnician program OR An associate's degree, or higher, in one of the chemical or biological sciences AND - one year

NERA Associate - Human Capital Recruiting 2 Locations posted: Posted 3 Days Ago

Acceleration Center - Advisory National - Jira Consultant - Senior Associate Ciudad de México, Mexico Join our team as a Senior Associate, Jira Consultant and drive delivery excellence with Atlassian Jira Cloud solutions. Leverage your expertise in automation, governance, and enterprise integration to optimize workflows and support business transformation. Collaborate with cross-functional teams and lead impactful projects in a dynamic, fast-paced environment.

Clinical Biospecimen Operations Associate Austin, TX POSITION SUMMARY: The Clinical Biospecimen Operations Associate executes oncology clinical research studies, including coordination of all operational activities required for tracking, testing and reporting clinical trial samples. This position will perform required job duties with oversight from the Pharma Operations Team Leader and will work closely with internal and external central testing laboratories, vendors, Data Management, Product Management, Engineering and external collaborators in compliance with the study protocol(s), SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES: - Maintain oversight of all study sample operational activities including planning, coordinating and tracking clinical trial sample testing to ensure results are provided within agreed upon TAT - Work with Data Management to develop and maintain dashboards and KPIs representing metrics and trends related clinical trial sample testing and the status of clinical studies and present to study teams and management teams, as needed. - Meticulously track clinical trial samples from sample receipt to result reporting to investigator sites and/or external collaborators (and sample return, if applicable) - Utilize operational and project management skills to anticipate, investigate and resolve issues to ensure deliverables and TAT are met; raise issues to Pharma Operations Team Leader - Responsible for handling data files to support timely result reporting - Review and provide input to clinical study protocol for sample collection requirements and alignment with the SOW, study plans and company policies - Administer clinical trial supplies related to biospecimen collection, processing, shipment, and storage as, well as maintenance of associated tracking information

Business Development Associate II Diazyme, an affiliate of General Atomics, is a cGMP and ISO 13485 certified medical device manufacturer. Diazyme uses its proprietary enzyme technologies to develop diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. Their products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes. Join Diazyme - Innovating Diagnostics for a Healthier World! We are seeking a dynamic Regional Sales Representative - Diagnostic Medical Devices to drive business growth and build strong customer relationships across the Midwest Region : OH, IN, KY, MI. In this role, you'll play a pivotal part in identifying new opportunities, developing strategic business plans, and delivering innovative diagnostic solutions to government and commercial agencies. If you're passionate about sales, thrive in a fast-paced environment, and want to make a meaningful impact in healthcare, we want to hear from you! DUTIES & RESPONSIBILITIES: - Develops market/product line business plans and capture plans to support sales in designated market segments. Advises management on status or action required in connection with existing and potential sales programs. - Identifies potential customers to develop and fosters partnerships. Analyzes market data to identify trends/opportunities and provides input for strategic direction. - Creates market analyses presentations. May prepare and present company product briefings and conducts facilities tours for visitors. - Assists in supplying business development input and administrative control for specific projects within the group. - Coordinates promotional activities including participation in trade shows, advertising,

Sr Phlebotomist - New Orleans, LA New Orleans, LA POSITION SUMMARY **This position is located on site in New Orleans, LA** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access

Director, Clinical Science US Remote POSITION SUMMARY: We are seeking a Director, Clinical Science to architect trial strategies and protocol execution for our oncology molecular diagnostics portfolio, with a dedicated focus on signal Studies and pipeline expansion. This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA) technology, transforming population scale genomic profiles into standard-of-care screening benchmarks. Reporting directly to the Senior Director of Clinical Science, you will lead the strategic alignment and tactical delivery of early and late-stage oncology diagnostics protocols. Operating with an active builder mindset, this position co-develops clinical program strategy and drives collaborative execution across clinical development, clinical operations, biostatistics, and translational data science teams. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture - Design robust clinical study concepts, specifying overall design parameters, schedules of assessments, trial objectives, clinical endpoints, and patient eligibility criteria - Lead clinical development activities and protocol design for oncology Signal Studies and portfolio development - Collaborate cross-functionally to author clinical study protocols, informed consent documents, and technical amendments for internal governance review - Deliver technical protocol validation training to internal teams and contract research organizations (CROs), and guide case report form (CRF) layout configurations - Ensure study manuals conform directly to protocol specifications and engage primary clinical investigators during initial trial design phases Data Interrogation and Cross-Functional Alignment - Synthesize protocol requirements from investigators, clinical partners, and regulatory bodies, resolving conflicting operational priorities by anchoring team alignment strictly in data - Partner with cross-functional technical teams to execute

Supervisor, Test Coordinator - Houston, TX Houston, TX Test Coordinator Supervisor - Houston, TX Position Summary The Supervisor for the Test Coordination Team will be responsible for leading and supporting a team of Test Coordinators, ensuring excellence in patient care coordination, phlebotomy services, and administrative operations. This role focuses on day-to-day team management, operational efficiency, compliance, and the development of team members. The Supervisor acts as the primary escalation point for internal and external queries, supporting seamless collaboration between field teams, patients, and operational departments. This position requires strong organizational, leadership, and communication skills, and will include up to 50% travel to support audits, onsite visits, and team training initiatives. Primary Responsibilities Team Leadership & Management - Provide daily supervision and support to the Test Coordinator team. - Serve as the first line of escalation for operational issues, patient and account inquiries, and procedural uncertainties. - Conduct biweekly 1:1 meetings with each direct report to promote engagement, identify training needs, and track performance. - Review and approve employee timecards and manage scheduling to align with clinic and organizational requirements. Operational Oversight - Ensure Test Coordinators maintain compliance with specimen handling protocols, EMR documentation, and patient identification practices. - Monitor key metrics and proactively mitigate issues that could impact operational performance. - Oversee supply chain needs, including ordering and tracking supplies for all test coordination activities. Quality Assurance & Audit Support - Assist with the coordination and execution of internal and external audits - Conduct regular quality checks on patient coordination

Sr Phlebotomist - Marrero, LA US Remote POSITION SUMMARY **This position is not remote, it is located in Marrero, LA** A Sr Phlebotomist serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures. PRIMARY RESPONSIBILITIES - Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel. - Verifies patient by reading patient identification. - Obtains blood specimens by performing venipunctures and finger sticks. - Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures. - Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed. - Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes. - Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations. - Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders. - Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. - Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. - This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI

Software Engineer (Jira) Singapore Summary: - Jira Software Engineer with deep expertise in Jira software engineering to administer and enhance Jira Cloud environment. - This role will focus on improving workflows, building automation, and optimizing Jira configurations to support efficient project tracking and collaboration. - Strong scripting skills, hands-on experience with Jira automation, and a deep understanding of how to leverage Jira Cloud capabilities to meet organizational needs. Key Responsibilities: - Administer and maintain Jira Cloud, including user management, permissions, and project configurations. - Design, implement, and optimize Jira workflows, custom fields, screens, and schemes to align with business processes. - Build and maintain automation rules using Jira Automation, scripting, and REST APIs to streamline operations and reduce manual effort. - Develop and manage integrations between Jira and other enterprise tools (e.g., Confluence, GitHub, ServiceNow). - Collaborate with stakeholders to gather requirements and translate them into scalable Jira solutions. - Monitor system performance, troubleshoot issues, and ensure data integrity across Jira projects. - Document configurations, automation scripts, and best practices for long-term maintainability. - Provide training and support to users, ensuring effective adoption of Jira features and workflows. Skillset (Must have) - Possess a degree in Computer Science, STEM, or related field. - At least 3 years of hands-on experience administering Jira Cloud in a production environment. - Strong proficiency in scripting languages (e.g. Python, JavaScript) for automation and integration. - Proven experience in building Jira automation rules and using REST APIs and webhooks for custom integrations. - Possess solid