4 Sample Tracking Jobs

You will be supporting the Study Lead in TCO studies to ensure all trial deliverables are met according to timelines, budget, operational procedures, and quality standards. Your role will involve assisting TCO CSD, CSaD, and CSTL in the development of study documents, tools, guidelines, and training materials. You will also be responsible for managing clinical study material and implementing issue resolution plans. Under the supervision of CSD, CSaD, and CSTL, you will play a key role in preparing CSR appendices. Additionally, you will be setting up and maintaining appropriate study tracking forms, including enrollment logs, site and vendor contact lists, drug shipping logs, and team membership lists. You will also support in managing interactions with relevant functions, drug tracking, creation and maintenance of HQ TOC, and timely completion of TMF. Your responsibilities will also include assisting in trial data analysis and reporting, meeting scheduling, distribution of meeting agendas/minutes, preparation, distribution, and archiving of study tools, financial management, forecasting, vendor management activities, and PK and biomarker sample tracking. You may also support selected tasks for other ClinOps functions. Novartis is dedicated to helping people with diseases and their families by fostering a community of smart, passionate individuals like you. By collaborating, supporting, and inspiring each other, we aim to achieve breakthroughs that positively impact patients" lives. If you are ready to contribute to creating a brighter future, join our Novartis Network to stay connected and informed about suitable career opportunities. As part of Novartis, you will have access to benefits and rewards outlined in our handbook to support your personal and professional growth. We are committed to providing reasonable accommodations to individuals with disabilities during the recruitment process or while performing essential job functions. Please reach out to [email protected] with your accommodation request and the job requisition number. Novartis is dedicated to building an outstanding, inclusive work environment with diverse teams that reflect the patients and communities we serve.,

You have a great opportunity to join our team as a Developer specializing in Thermo Fisher Scientific SampleManager LIMS with 5+ years of experience. Your primary responsibilities will include configuring, customizing, and maintaining SampleManager LIMS to support laboratory operations efficiently. You will be tasked with developing and optimizing LIMS workflows, sample tracking, and data management solutions to enhance lab efficiency. Collaboration with scientists, lab managers, and IT teams is essential to implement and enhance LIMS functionalities effectively. In this role, you will be integrating SampleManager LIMS with various laboratory instruments, ERP systems, ELN, and other enterprise solutions. Ensuring regulatory compliance, including 21 CFR Part 11, GxP, and HIPAA, and maintaining audit trails within the LIMS environment will be a crucial part of your responsibilities. Troubleshooting LIMS-related issues, providing technical support, and implementing system upgrades will also be key tasks. Additionally, you will be developing custom scripts, plugins, or automation tools using VGL scripting language for SampleManager LIMS, SQL, or preferably C#/.NET. Experience with REST APIs, web services, and cloud-based solutions such as AWS/Azure for LIMS data management is highly desirable. You will play a vital role in maintaining data integrity, security, and scalability of LIMS deployments in regulated lab environments. It would be advantageous to have skills in C#/.NET programming for LIMS customization and automation, familiarity with VGL scripting language, exposure to cloud computing (AWS, Azure), and DevOps tools like CI/CD, Docker, and Kubernetes. Knowledge of bioinformatics, analytical chemistry, or clinical research workflows, as well as an understanding of HL7, ASTM, or OPC-UA for instrument interfacing, would be considered beneficial for this role.,

As a part of Strand Life Sciences, you will be contributing to the cutting-edge Genomics field with a global impact on human health. Your role will involve performing and overseeing karyotyping and fluorescence in situ hybridization (FISH) analysis on various samples, including Peripheral blood, prenatal, and haematological malignancy samples. It will be crucial for you to accurately analyze, interpret, and report cytogenetic findings using ISCN Nomenclature while developing, validating, and implementing new cytogenetic techniques. You will be responsible for ensuring timely processing and reporting of cytogenetic tests, maintaining defined turnaround times (TAT). Additionally, you will play a key role in preparing standard operating procedures (SOPs), validation reports, and relevant documents as necessary. Utilizing LIMS for sample tracking and workflow integration will be essential to streamline processes effectively. In this role, you will also be accountable for the proper handling, maintenance, and care of laboratory instruments, including routine checks and troubleshooting. Managing inventory to ensure the availability of reagents, consumables, and critical supplies will be part of your responsibilities. It will be important to document assay failures, delays, corrective actions, and quality improvement initiatives comprehensively while proactively communicating any process delays or failures with stakeholders. Collaboration with cross-functional teams to enhance laboratory operations and troubleshoot issues will be a significant aspect of your work. Ensuring compliance with regulatory standards such as CAP/CLIA, NABL, and other relevant quality assurance guidelines will be crucial. Moreover, you will have the opportunity to train and mentor junior technologists and team members. Joining Strand Life Sciences will offer you an innovative and open culture within a multicultural environment, allowing you to make a fundamental impact on human health. You can look forward to vibrant multidisciplinary scientific interactions, continuous learning opportunities, and a collaborative environment where your contributions can truly make a difference. Along with these, you will receive a competitive salary and generous benefits as part of our team.,

Role & responsibilities As a Product Development Executive , you will be the linchpin in managing all aspects of trims, paper packaging, and polybags for garment products. With your specialized knowledge spanning these categories and a proven 5-year track record, you will: Lead the sourcing, selection, and development of trims , including labels, zippers, buttons, elastics, and decorative accentsensuring alignment with design aesthetics, quality benchmarks, and cost targets. Manage paper packaging and polybag strategy , from concept to executionworking with packaging suppliers to develop materials that are functional, brand-appropriate, compliant (e.g., labeling, printing, sustainability standards), and optimized for cost-efficiency. Oversee end-to-end sample development , coordinating closely with sourcing markets to develop prototypes, gather lab dips, finalize packaging samples, and obtain approvals for production. Collaborate with internal stakeholders designers, merchandisers, QA, production, and logistics—to integrate trims and packaging seamlessly into product tech packs, cost sheets, and time plans. Preferred candidate profile