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Edition 19 – celebrating women who are breaking barriers in healthcare!

After the successful 18th edition of the Fast Forward Guest Series, we’re back with Edition 19 – celebrating women who are breaking barriers in healthcare! Theme: Empowering Women in Healthcare: Leadership, Innovation & Impact Speaker: Sameena Khanam, Deputy Director – Brand & Corporate Communications, Zulekha Hospital (DUBAI, UAE) Date: March 24, 2025 | ⏰ 7–8 PM IST | 5 PM Dubai Time
Meeting Link: https://zoom.us/j/97093662654?pwd=3fVaAaKHukabTdnjs6YVrSFSKH0HYs.1
 Meeting ID: 970 9366 2654
Passcode: 005481 About the speaker: With 18+ years of experience across India & UAE, Sameena is a powerhouse in communications and leadership.  Join us for an inspiring session that celebrates resilience, impact, and the spirit of women in healthcare. Don’t miss it!

Placements

It gives us immense pleasure to announce that Croissance Clinical research has shown interest in hiring talent from Clinilaunch Research Institute.

Dear Student,  Greetings! It gives us immense pleasure to announce that Croissance Clinical research has shown interest in hiring talent from Clinilaunch Research Institute. About – Croissance Clinical research About company: Croissance Clinical research is a full-fledged CRO providing services for Pharmaceutical, bio- technology and medical devices companies. Croissance Clinical Research applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments. Our experienced project managers and the team leaders will ensure, that all the services are conducted in accordance with the study protocol, ICH-GCP guidelines and applicable regulatory requirements. Company: Croissance Clinical research Website: http://www.croissancecr.com Job Type: Private Job Role: CDM, Trainee Clinical SAS Industry: Biotechnology Research Job Priority: Normal Job Nature: Work from Office Job Mode: Full Time, Work from Office. Job Position: Permanent Job Location: Hyderabad, Telangana Job Type: Full-Time Qualification: B,Sc Bio technology, M,Sc Bio technology, B,Sc Statistics, M,Sc Statistics, B Tech Biotechnology- for SAS, All life Science for CDM Date Published: 24-3-2025 Valid Through: 24-3-2025 (06:00 PM) Interview mode:  Walk in Experience: Only Freshers Salary: As per industrial norms JD for Trainee Clinical SAS  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: Bachelor’s degree in Life Sciences, Computer Science, Statistics, Mathematics, or related field. 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). JD for Clinical Data Management  Job Summary: Key Responsibilities: Data Management Support: Assist in the setup, maintenance, and troubleshooting of clinical trial databases, ensuring the accuracy and consistency of data collected throughout the trial. Data Review & Validation: Help validate incoming data for completeness and consistency, and assist in identifying and resolving discrepancies. Case Report Form (CRF) Management: Support the creation, management, and revision of Case Report Forms (CRFs) to ensure they meet study requirements. Electronic Data Capture (EDC): Assist in the implementation and monitoring of EDC systems, ensuring proper data entry and resolving any issues related to the system. Query Management: Assist in generating and managing data queries for clinical trial sites, ensuring timely resolution and follow-up. Study Documentation: Help maintain accurate records of data management activities, ensuring compliance with regulatory requirements and internal guidelines. Collaboration: Work with cross-functional teams including clinical operations, biostatistics, and regulatory affairs to ensure timely and accurate data collection, review, and reporting. Compliance with Regulations: Ensure data management processes comply with industry regulations such as Good Clinical Practice (GCP), 21 CFR Part 11, and ICH guidelines. Reporting & Tracking: Assist in preparing reports and tracking progress to ensure data management milestones are met according to timelines. Requirements: Skills: Strong attention to detail and accuracy. Good organizational skills with the ability to manage multiple tasks. Ability to work collaboratively within a team. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Attributes: Strong communication skills, both written and verbal. Eagerness to learn and develop in the clinical research field. Ability to adapt to new software and technologies. Preferred (but not required): Familiarity with clinical trial processes and data management terminology. Experience with Electronic Data Capture (EDC) systems or clinical data management software is a plus. Application Link: https://forms.gle/9Zp9geKxbqXPdUGD7 In Case of any Queries Contact Priyanka C - 8904527576/ Mugesh raj – 8951764077  Regards, Placement Team

Guest Series

After the successful 18th edition of the Fast Forward Guest Series, we’re back with Edition 19 – celebrating women who are breaking barriers in healthcare!

Theme: Empowering Women in Healthcare: Leadership, Innovation & Impact Speaker: Sameena Khanam, Deputy Director – Brand & Corporate Communications, Zulekha Hospital (DUBAI, UAE) Date: March 24, 2025 | ⏰ 7–8 PM IST | 5 PM Dubai Time
Meeting Link: https://zoom.us/j/97093662654?pwd=3fVaAaKHukabTdnjs6YVrSFSKH0HYs.1 Meeting ID: 970 9366 2654 Passcode: 005481 About the speaker: With 18+ years of experience across India & UAE, Sameena is a powerhouse in communications and leadership.  Join us for an inspiring session that celebrates resilience, impact, and the spirit of women in healthcare. Don’t miss it!

Session Updates

MC demo Session - 5:30PM (24th March 2025)

Clini Launch Official is inviting you to a scheduled Zoom meeting. Topic: MC module - Dr. Ujawala Time: Mar 24, 2025 05:30 PM India Join Zoom Meeting https://zoom.us/j/98884476371?pwd=y2zXCpUmM8IaVq7odJAZJPu8GJjftz.1 Meeting ID: 988 8447 6371 Passcode: 360217

Session Updates

MC demo Session - 4PM (24th March 2025)

Clini Launch Official is inviting you to a scheduled Zoom meeting. Topic: MC demo  - Haritha  Time: Mar 24, 2025 04:00 PM India Join Zoom Meeting https://zoom.us/j/98944074008?pwd=kGbWqgFMoe4IiUoJoSA016dOCChlLE.1 Meeting ID: 989 4407 4008 Passcode: 725564 --- One tap mobile +13863475053,,98944074008#,,,,*725564# US +15074734847,,98944074008#,,,,*725564# US --- Dial by your location • +1 386 347 5053 US • +1 507 473 4847 US • +1 564 217 2000 US • +1 646 931 3860 US • +1 669 444 9171 US • +1 669 900 6833 US (San Jose) • +1 689 278 1000 US • +1 719 359 4580 US • +1 929 205 6099 US (New York) • +1 253 205 0468 US • +1 253 215 8782 US (Tacoma) • +1 301 715 8592 US (Washington DC) • +1 305 224 1968 US • +1 309 205 3325 US • +1 312 626 6799 US (Chicago) • +1 346 248 7799 US (Houston) • +1 360 209 5623 US Meeting ID: 989 4407 4008 Passcode: 725564 Find your local number: https://zoom.us/u/abFRv9mpNe

Guest Series

Fast Forward Guest Series - SPARK - Guest Series(22nd March 2025)

Topic: WILA SPARK SERIES | Suman Rakshit| Baxter International Inc.|  Overview on cybersecurity in healthcare followed by a Q&A session Time: Mar 22, 2025 07:00 PM Mumbai, Kolkata, New Delhi Join Zoom Meeting https://zoom.us/j/94233201884?pwd=oufIqKLQieGjLjP5bmNwoAaxaGFbg6.1 Meeting ID: 942 3320 1884 Passcode: 216845 ---  

Guest Series

Fast Forward Guest Series - SPARK - Guest Series(19th March 2025)

  Kindly note down if you are having regular session at 7-8pm then kindly attend your regular sessions(skip Fast Forward Guest Series) 🗓 Date: 19th March, 2025 ⏰ Time: 7:00 PM - 8:00 PM IST 🔊 Speaker: Ms. Devasmita Das 🎓 Theme: Women in Technology: Breaking Barriers & Leading Innovation Topic - Cyber Ethics & AI: Addressing Security & Privacy Challenges Across Industries Join this session to explore how AI is reshaping cybersecurity and data privacy. Discover the key security and ethical challenges industries face in protecting sensitive data and maintaining trust. Learn about emerging career opportunities in AI and cybersecurity, and uncover best practices to strengthen data protection and ensure compliance with evolving regulations. Please join the Session from below Link: Zoom Link: https://zoom.us/j/94358598649?pwd=YaqoAMO2dVy5QuFSFsSsAaHYa7S0gy.1

Placements

It gives us immense pleasure to announce that Portea Medicals has shown interest in hiring talent from Clinilaunch Research Institute

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: 18/3/2025   Valid Through:  19/3/2025  Before 4PM NOTE: CLRI Format Resume is Mandatory In Case of any Queries Contact Priyanka Naik - 07204412729 and Sushree - 8904982932 Regards, Placement team

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