5 Signal Analysis Jobs

You will be providing medical safety expertise to Sponsors of drugs, devices, and combination products during the post-marketing period. Your responsibilities will include conducting primary medical review of cases, assessing seriousness, listedness/labeling, causality, adverse event coding, and narrative review. Daily case data update and documentation, along with feedback in appropriate trackers/tools, will be essential for efficient tracking and workflow management. It will be your responsibility to ensure the quality, compliance, and productivity of all assigned deliverables within the expected SLAs and KPIs. After a tenure of 1 year, you will provide training and guidance to the case processing team on medical aspects of case processing. Additionally, you will perform aggregate and signal analysis activities to support single case processing and maintain a culture of high customer service. Qualifications: - Bachelor's degree in medical science, MD, DO, or equivalent degree. - Relevant experience may be considered in lieu of educational requirements. - Language proficiency in English at ILR level 3+ for speaking and ILR level 4+ for writing/reading. Experience: - Working knowledge of medical sciences, diagnosis, therapeutics, drug treatments, and procedures. - Understanding of regulatory requirements for Clinical Research. - Familiarity with ICH-GCP guidelines. Preferred Qualifications: - 1 to 2 years of Clinical practice experience. Physical Demands/Work Environment: - Work may be in an office or home-based environment as requested by the line manager. For more information on our Equal Employment Opportunity (EEO) and Accommodations request, please refer to our website.,

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Preparation of responses to PRAC assessment reports and other Authority requests (e.g., referrals, etc). Performing signal detection and signal analysis of safety data, provide the appropriate expert advice as well as assisting in communication with regulatory agencies when the new data has an effect on the risk-benefit balance. SOP services/writing and review of SOPs, WIs and related documents and training material in the area of pharmacovigilance for clients (including implementation and training. Development of customer-specific solutions and processes in cooperation with clients. Build, develop and maintain working relationships with clients. Ensure client satisfaction and compliance with legal and regulatory requirements. Representation of the company and the team with clients, authorities and professional institutions. Inform the Head of the Pharmacovigilance Team/Service Line Lead regularly about systematic problems that could jeopardize an appropriate coordination of tasks and to present solutions. Management of parts of a project or the complete project. Fulfilling highly complex, sophisticated tasks within the area of pharmacovigilance. Trigger a non-conformity when any performance deviation from the target KPI (Key Performance Indicator) is detected, issue evaluation and root cause analysis, assign corrective actions with a due date to the most appropriate employee, ensure that all agreed actions are completed by the due date. Communicate proactively with clients about the status of the project and provide solutions to address process deviations, quality issues and inefficiencies. Development of processes and/or tools within the area of pharmacovigilance in collaboration with the Head of the team and the Head of the Pharmacovigilance Department. Design and prepare Standard Operational Procedures, Working instructions and Client Specifications for Pharmacovigilance processes, ongoing revisions and implementation of updates. Contribute to achievement of departmental goals, Identify and discuss out-of-scope activities that affect project invoicing. Client audits (preparation of the audit, defend it, review the audit report and follow action plan). Contribute to resource needs and resource allocation to ensure compliance, identification and implementation of process efficiency needs. Minimum 4 years of experience in relevant field. Experience in writing and reviewing PBRER, PSUR, RMP, PADER and ACO Experience in Preparation of responses to PRAC, other authority requests Experience in writing and review SOP, preparing training material Build update and maintain working relationships with client What Cencora offers Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements. Full time Affiliated Companies Affiliated Companies: PharmaLex India Private Limited Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The companys continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [HIDDEN TEXT]. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Show more Show less

As a Junior Research Fellow (JRF) at Opto-Biomedical Microsystem (OBMS) Laboratory, your primary focus will be on developing instruments for various biomedical applications such as screening, diagnosis, monitoring, and point-of-care diagnostics. Additionally, you will work on image and signal analysis for drug screening and testing applications, as well as the fabrication of microfluidic devices. The lab is well-equipped with state-of-the-art tools including a high-end Workstation with 32 GB Graphics card ADA GPU, High-Speed Imaging Camera capable of capturing up to 14000 frames per second, Polarized He-Ne laser source of 20 mW, High Power white light sources, Multiple Vibration Isolation Optical Table, Various Optical and opt mechanics components, and Various 3D printers including Industrial grade Bambu Labs, Creality 3D printer, Resin 3D printer, and High Power Laser Engraver of 40 Watts. This is a full-time on-site role for a Junior Research Fellow (2 years) at OBMS Laboratory. Your responsibilities will include developing and testing instruments for biomedical applications, microfluidic devices, and image and signal analysis. You will also be actively involved in conducting research and publishing results. Candidates with experience in dealing with Optical components, Applied physics, Optics, Microfluidics, and a strong understanding of biomedical applications and technology will have an edge in the recruiting process. Additionally, experience in developing and testing biomedical instruments, microfluidic devices, image and signal analysis, and the ability to conduct research and publish results are essential qualifications for this role. The successful candidate will have the opportunity to enroll in a Ph.D. program at NIT Rourkela if all criteria are fulfilled. This position is available under the sponsored project titled "Innovating Indigenous Portable Microfluidic Absorption Flow Cytometer for Multi-diseases Detection at Point-of-Care" supported by ANRF / SERB, India. If you possess a Bachelor's or Master's degree in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Physics, or a related field, along with excellent written and verbal communication skills, and the ability to work as part of a team, we encourage you to apply by filling out the application NITR/SR/2025/Advt./23BM060/L/051. For further details or inquiries, you can contact Dr. Earu Banoth, Fulbright Fellow-2019, Senior Member IEEE and OPTICA, and Assistant Professor at the Department of Biotechnology Medical Engineering, NIT Rourkela via email at banothe@nitrkl.ac.in or phone at +91 8861543837 / 661-246-2299.,

You will be responsible for supervising and monitoring the design, deployment, and maintenance of network infrastructure as part of the Bharat Net Project. This includes overseeing the installation, configuration, and testing of routers, switches, GPON/OLT/ONT. You will conduct field-level quality checks to ensure project compliance and support troubleshooting for network connectivity and configuration issues. Monitoring performance metrics such as latency, signal strength, and throughput will also be crucial. Maintaining detailed site visit logs, test reports, and quality documentation is essential for this role. You will need to ensure that network security protocols and standard practices are followed at all times. Coordination with PIAs, OEMs, and State NOC for validations and performance reviews will be part of your responsibilities. Additionally, traveling across district project sites as required under the Bharat Net implementation plan is expected. Preferred skills for this position include knowledge of Fiber Optics, GPON, IP/MPLS, L2/L3 Networking, as well as hands-on experience with network testing tools and signal analysis. Strong communication, problem-solving, and teamwork skills are essential, along with a willingness to travel extensively across project locations. If you meet the qualifications and are eager to contribute to the Bharat Net Project by ensuring the smooth operation of network infrastructure, we encourage you to apply for this position.,

You will be joining Machinellium Mavericks Projects and Consultants Inc. as a Mechatronics Engineer, where your main responsibility will be the research, design, development, and testing of advanced Intelligent Systems. Your role will involve identifying areas for enhancement in existing designs, creating and executing new designs, and conducting thorough testing. Your innovative mindset will be crucial in developing cutting-edge concepts that showcase forward-thinking and creativity. Your key skills should include experience in the research, design, implementation, and testing of AI systems. Moreover, you should be familiar with control system analysis and design, instrumentation development, sensor integration, data acquisition, and signal analysis. Your proficiency in data-driven product development is essential for this role. Additionally, you should have a deep understanding of application platform technologies such as Visual Studio, Blend, Windows apps, Azure, Windows Phone, iOS, and Android. In this role, you will be expected to create pioneering designs that can be effectively implemented and sustained at the conclusion of the design phase. Your strong analytical abilities, organizational skills, and documentation expertise will be valuable assets in this position. Furthermore, effective communication skills and the ability to perform well under pressure are key qualities that will contribute to your success in this role.,