New Modules from 1st april 2025
Hello everyone this is to inform you that new module for 1st april 2025 has been updated (wherever applicable)into your account under learn section.kindly check that.
Hello everyone this is to inform you that new module for 1st april 2025 has been updated (wherever applicable)into your account under learn section.kindly check that.
Dear Students, Please be informed that 31st March will be a holiday on the occasion of Eid. ๐โจ Enjoy the festive day with your loved ones, and we wish you all a joyous and blessed Eid! ๐๐ Regular classes will resume from 1st April as per schedule.
Demo Session for Clinical Research has been planned today (29th March 2025) at 2:00 PM. Kindly attend the session give us the feedback. Link for the sesion - https://zoom.us/j/91765509724?pwd=YvDbKaEbIs7qr2KvNHRZPSq9OEXW9k.1
Demo Session for Medical Coding has been planned tomorrow(29th March 2025) at 11:30 AM. Kindly attend the session give us the feedback. Link for the sesion - https://zoom.us/j/93287080005?pwd=BrPyClHXz8U4bNDvutRIAiV3ZrU9nU.1
Dear Student, Greetings!! It gives us immense pleasure to announce that Portea Medicals has shown interest in hiring talent from Clinilaunch Research Institute About: Portea Medical delivers quality care with compassion. We bring quality medical care into our patients’ homes and aim to make primary healthcare not only more accessible, but also more affordable and accountable to our patients’ needs. Website: http://www.portea.com Job Type: Private Hiring For: Portea Medicals Job Role: Clinical Quality Executive Industry: Hospitals and Health Care Job Priority: Normal Job Nature: Office Job Mode: Full Time Job Position: Permanent Job Location: Bengaluru Salary: CTC 3.2 lpa - 4 lpa Experience Range: Fresher/Experienced (0-2 years) Qualification: All Life science Background Should be proficient in English and Hindi Language No. of Open Positions: 2 JOB RESPONSIBILITIES : * Serve as the compliance owner, overseeing the monitoring of transactions to identify Pharmacovigilance issues, adverse events (AE), and product quality complaints related to medical drugs. * Evaluate the health of processes and provide constructive feedback to candidates and team leaders for continuous improvement. * Conduct root cause analysis for process deviations, develop action plans, implement resolutions, and drive ongoing process improvements. * Document process insights and lead initiatives aimed at enhancing operational efficiency and quality. * Manage and resolve escalated concerns, issues, and requests from both internal and external stakeholders. * Perform compliance monitoring for pharmaceutical and medical equipment warehouse operations across all branches. * Identify training needs and facilitate process calibration sessions among key stakeholders. * Utilize Excel for data analysis and leverage insights into patient experience to prioritize critical improvement initiatives. * Demonstrate exceptional listening and analytical skills, effectively communicating with stakeholders regarding process quality issues. * Conduct Net Promoter Score (NPS), customer satisfaction (CSAT), and medical investigation calls to patients, clients, and other relevant parties. * Prepare executive-level performance reports on respective processes and share updates with the lead auditor for presentation during weekly and monthly review meetings Interview Mode: Walk in Interview at , Address: 69/B, 1st Cross Rd, Domlur I Stage, 1st Stage, Domlur, Bengaluru, Karnataka 560071 Application Link: https://forms.gle/ks62YLgvxb6nYLqr5 Date Published: 28/3/2025 Valid Through: 29/3/2025 Before 10AM NOTE: The candidates are ready to appear for the Interview tomorrow i. e. 29th March can only apply. In Case of any Queries Contact Priyanka Naik - 07204412729 and Sushree - 8904982932 Regards, Placement team
Dear Student, Greetings!! It gives us immense pleasure to announce that Palamur Biosciences Private Limited has shown interest in hiring talent from Clinilaunch Research Institute. About : Palamur Bioscience scientific team members are highly experienced in both field of specialization and quality systems like GLP / NABL. All the studies are executed by GLP trained scientific personnel with an aggregate experience of close to 100 years of expertise in study design and execution. Animal technicians and handlers are trained as per FELASA and approved SOPs. Your drug with the regulatory authorities as well as studies on your chemical for its registration with the European Chemicals Agency ECHA for the REACH program. We´ll also test your food additive according to the European Food Safety Authority EFSA. Website: http://www.palamurbio.com/ Job Type: Private Hiring For: Palamur Biosciences Private Limited Job Role: ๐๐ถ๐ผ-๐๐ป๐ฎ๐น๐๐๐ถ๐ฐ๐ฎ๐น ๐๐ฎ๐ฏ ๐ฆ๐ฐ๐ถ๐ฒ๐ป๐๐ถ๐๐ Industry: Research Job Priority: Normal Job Nature: Office Job Mode: Full Time, Work from Office Job Position: Permanent Job Location: Mahabubnagar, Hyderabad Telangana Salary: As Per Company Norms Qualification: life science background Date Published: 26-3-2025 Valid Through: 27-3-2025 Till 11 am *Application Link: https://forms.gle/6x5YG4hK58nSfqw17/ Job Description: We are seeking a skilled and detail-oriented Bio-Analytical Lab Scientist to join our dynamic team. The ideal candidate will be responsible for conducting bio-analytical method development and validation, performing sample analysis, and ensuring data accuracy and compliance with laboratory standards. ๐๐ฒ๐ ๐ฅ๐ฒ๐๐ฝ๐ผ๐ป๐๐ถ๐ฏ๐ถ๐น๐ถ๐๐ถ๐ฒ๐: โช๏ธ Perform bio-analytical testing using LC-MS/MS instruments. โช๏ธ Analyse biological samples and interpret data. โช๏ธ Maintain lab records and ensure quality control compliance as per the GLP. โช๏ธCollaborate with cross-functional teams on research projects. Note : CLRI Resume is Mandatory In Case of any Queries Contact Sushree - 8904982932 Priyanka - 7204412729 Regards, Sushree Placement Team
Dear Students, Please note that today’s Guest Session at 7:00 PM is mandatory for everyone to attend. It is essential for your learning and participation is required. Apart from this session, all other classes will be held at their regular scheduled times. Make sure to be on time and make the most of this opportunity! ๐ Time: 7:00 PM (Guest Session) ๐ Attendance: Mandatory For reference please find the link - https://zoom.us/j/95700228482?pwd=8HNppBUS1ftMMTQY4RTmZfK0E5iug4.1 Meeting ID - 957 0022 8482 Passcode - 965721 See you all there!
Dear Student, Greetings!! It gives us immense pleasure to announce that Axis Clinicals has shown interest in hiring talent from Clinilaunch Research Institute. Company Details: Axis Clinicals, a renowned name in the clinical research and bioanalytical industry, is offering an exciting opportunity for freshers (male) to join as Trainee Research Associates – Bioanalytical in Hyderabad. This role is ideal for candidates with a background in biological sciences, pharmacy, or clinical research who are looking to kickstart their careers in a dynamic and growing field. With a competitive salary range of INR 50,000 to 2 Lakhs per annum, this position is a great stepping stone for aspiring professionals. Website: https://axisclinicals.com/ Job Type: Private Hiring For: Axis Clinicals Job Role: SAS Programmer Industry: Bioanalytical Industry Job Priority: Normal Job Nature: Office Job Mode: Full Time Job Position: Permanent Job Location: Hyderabad Salary: 2.5LPA Experience Range: 0-4 Years (Fresher Only) Qualification: Msc in Statistics or Biostatistics & SAS Certified only Bond: 2-year bond with the requirement to submit the original 10th-grade mark sheet during the bond period. Job Summary: We are seeking a motivated and detail-oriented fresh graduate to join our team as a Trainee Clinical SAS Programmer. In this role, you will be responsible for assisting in the development, validation, and analysis of clinical data using SAS software in clinical trials. You will work closely with senior programmers and other cross-functional teams to ensure the accuracy and integrity of clinical trial data while adhering to regulatory guidelines. Key Responsibilities: * Assist in the development, testing, and maintenance of SAS programs to manage clinical trial data, including datasets, tables, listings, and figures. * Support the creation and validation of standard clinical trial datasets, including SDTM, ADaM, and other regulatory-compliant formats. * Participate in the analysis and reporting of clinical trial data in accordance with the project specifications. * Collaborate with the clinical data management, biostatistics, and other departments to ensure seamless data flow and integrity. * Perform data review and quality checks to ensure accurate data submission. * Assist in generating datasets, reports, and analysis outputs for submission to regulatory authorities (e.g., FDA, EMA). * Follow Good Clinical Practice (GCP), 21 CFR Part 11, and other regulatory standards in programming activities. * Work with the senior team members to troubleshoot and resolve any programming issues or data discrepancies. * Participate in regular project meetings and contribute to status updates. * Document programming activities and outputs according to internal procedures and quality standards. Requirements: * Basic knowledge of SAS programming language is a plus. * Familiarity with clinical trial processes and terminology is an advantage. * Strong analytical and problem-solving skills. * Attention to detail and ability to handle multiple tasks simultaneously. * Good communication and interpersonal skills to work in a collaborative team environment. * A keen interest in clinical data analysis and programming. * Ability to learn quickly and adapt to new tools and technologies. * Preferred Skills (optional but advantageous): * Internship or project experience related to clinical data or SAS programming. * Exposure to clinical trial management systems or related software. * Knowledge of clinical data standards (e.g., CDISC, SDTM, ADaM). Date Published: 25-03-2025 Through: Valid: 26-03-2025 Before 11AM Note : CLRI Resume is Mandatory Application Link : https://forms.gle/WJdoaWjb6TYe6KNy8 In Case of any Queries Contact Harshitha - 8050234854 Regards, Harshitha Placement Team
Theme: Empowering Women in Healthcare: Leadership, Innovation & Impact Speaker: Dr. Lopa Mudraa Basuu, Global Advisor - CISO & DPO Advisory Services, Nexusnow.ai Date: March 25, 2025 Time: 7-8 PM link - https://zoom.us/j/95700228482?pwd=8HNppBUS1ftMMTQY4RTmZfK0E5iug4.1 Meeting ID - 957 0022 8482 Passcode - 965721 About the Speaker: Lopa Mudraa is a seasoned Security Evangelist with 20+ years of expertise in Information Security, Data Privacy, Risk Management, and Governance. She excels in enterprise security strategy, cyber defense, compliance (PCI DSS, ISO 27001, HIPAA), and risk governance. A thought leader, speaker, and award-winning professional *(Top 100 CISO, InfoSec Maestros, C|CISO of the Year), she is skilled in team building, stakeholder management, and executive leadership collaboration. Holding multiple global certifications (C|CISO, CRISC, CISM, CEH, QSA, ISO 27001 LA, ITIL), she is committed to driving security as a business enabler. Don't miss it!
Kindly attend the Fast Forward Guest Series as link is already posted in lms.