Vimal V. Email and Phone Number
Vimal V. work email
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Vimal V. personal email
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An innovative entrepreneur and transformative leader, blending scientific expertise with business acumen to drive multiple ventures and elevate industry standards. With a Doctorate in Biochemistry and deep expertise in Clinical Research and Quality Assurance, I have spearheaded initiatives that ensure regulatory compliance, data integrity, and patient safety across clinical development in leading biotech firms.As a serial entrepreneur, I have founded and scaled multiple successful ventures. Innovspace, the first coworking space in a tier-two region, set new benchmarks for collaboration and innovation, while Zita.ai, an AI-powered recruitment platform, is transforming the talent acquisition landscape with cutting-edge technology. My leadership in Infrastride, a real estate development company, and Nelli Farms, an agricultural venture, further highlight my ability to identify market gaps and create sustainable, high-impact solutions across diverse sectors.Whether in clinical research or entrepreneurship, I am driven by a passion for industry transformation. I thrive on building innovative, scalable solutions that address unmet needs and deliver measurable results. My work is a testament to the power of leadership and vision in driving meaningful change.My career has also been characterized by ethical leadership as the Vice Chair of an Institutional Ethics Committee. I've ensured the integrity of clinical trials through rigorous ethical oversight.As an angel investor in early-stage startups, I am committed to fostering innovation and supporting promising ventures.
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Chief Strategy Officer (Cso)Innvocept Global SolutionsCalifornia, United States
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Chairman | Innovspace | Sense7Ai | Infrastride | Nelli HillsAeon Indus Sep 2024 - PresentAs the Chairman of an innovative group of companies, I am redefining industry standards, driving unprecedented growth, and fostering cross-industry synergies. While my visionary approach has led to the success of each venture, now I am tasked with creating long-term value and driving positive change in every sector that we are engaged now. -
Founder/Member Board Of DirectorsInnovspace - Business Solutions/Coworking Feb 2017 - PresentCoimbatore, Tamilnadu, InAs the visionary Founder of Innovspace, I broke new ground by launching the first-ever coworking space in Coimbatore, a tier-two region. My innovative approach has revolutionized workspace solutions in an underserved market, setting a new standard for quality and accessibility. With a keen eye for strategic planning, location selection, and aesthetic design, I've cultivated a thriving community of freelancers, remote workers, and small businesses. My leadership extends beyond daily operations to encompass data-driven marketing and financial stewardship. By adeptly navigating market challenges and leveraging unique opportunities, I've positioned Innovspace as a leader in the coworking industry -
Sr. Director, Gcp/ PvAlumis Dec 2022 - Aug 2024South San Francisco, California, UsAs a seasoned Head of Clinical QA, my leadership is defined by a robust technical acumen and a strategic approach to quality assurance in Good Clinical Practice (GCP), Pharmacovigilance (PV), and Computer System Validation (CSV). I spearhead cross-functional teams, instilling a culture of excellence and compliance aligned with ICH guidelines, FDA regulations, and EMA standards. My leadership skills extend to risk-based auditing, CAPA management, and SOP development, ensuring that we meet and exceed industry benchmarks. With a focus on data integrity, patient safety, and regulatory compliance, I have successfully led initiatives that have elevated the quality of clinical development. -
Vice Chairperson, Institutional Ethics CommiteeSri Ramakrishna Hospital Jun 2018 - Jan 2023As the Vice Chairperson of the Institutional Ethics Committee, I bring a blend of ethical rigor and clinical expertise to oversee the integrity of clinical trials. My leadership is pivotal in ensuring compliance with ethical standards, informed consent processes, and regulatory guidelines. With a focus on patient safety and data validity, I collaborate with cross-functional teams to review and approve trial protocols, monitor ongoing studies, and evaluate adverse events. My role is instrumental in upholding the ethical principles that guide clinical research, making a significant impact on both patient outcomes and scientific validity. -
DirectorArcellx, Inc. Dec 2021 - Dec 2022Redwood City, California, UsAs the Director of Clinical Quality at Arcellx, a leader in the cell therapy oncology domain, I've set new standards for leadership in Clinical QA. My technical acumen and strategic approach have been instrumental in advancing Good Clinical Practice (GCP), Pharmacovigilance (PV), and Computer System Validation (CSV) within the organization. Leading cross-functional teams, I've instilled a culture of excellence and compliance that aligns with ICH guidelines, FDA regulations, and EMA standards. My specialized skills in risk-based auditing, CAPA management, and SOP development have not only met but exceeded industry benchmarks. With a steadfast commitment to data integrity, patient safety, and regulatory compliance, I've successfully elevated the quality of Arcellx's clinical development in the highly specialized field of cell therapy oncology -
Member Board Of DirectorsZita.Ai Jan 2021 - Nov 2022As the visionary Founder of Zita.ai, I conceptualized an AI-powered recruitment platform aimed at transforming the hiring landscape. While the idea was mine, its successful execution has been led by a high-caliber team that I've personally groomed. Together, we've developed a platform that modernizes and simplifies recruitment through essential ATS features and cutting-edge AI algorithms. My leadership has been instrumental not only in ideation but also in cultivating a team that has turned this vision into a reality, setting new industry standards for efficiency and effectiveness in talent acquisition. -
Director, Clinical QualityMyokardia Jun 2019 - Nov 2021Brisbane, California, UsAs the Director of Clinical Quality, I led the organization to a landmark achievement—the successful approval of the breakthrough drug Mavacampten. Leveraging technical expertise in Good Clinical Practice (GCP), Pharmacovigilance (PV), and Computer System Validation (CSV), I implemented risk-based auditing and CAPA management strategies that exceeded regulatory standards. My collaborative leadership united cross-functional teams and streamlined processes, resulting in accelerated timelines and impeccable data integrity. This culminated in meeting and surpassing compliance benchmarks, setting a new industry standard for clinical trial excellence. -
Member Board Of DirectorsSense7Ai Jan 2018 - Jul 2021Pleasanton, California, UsAs the Founder and Member of the Board of Sense7AI, I've been instrumental in steering the company's vision and strategy for delivering innovative, intelligent software solutions. My dual role allows me to blend entrepreneurial drive with governance oversight, ensuring not only the commercial success of our products but also long-term sustainability. Specializing in everything from digital product strategy to data analytics and UX design, I've led Sense7AI from concept to commercialization, empowering businesses to stay ahead of technological trends. My leadership is characterized by strategic acumen, operational excellence, and a keen focus on measurable outcomes, setting a high standard in the industry. -
Strategy Lead - Clinical Quality Assurance & Risk ManagementGenentech Dec 2008 - Jun 2015South San Francisco, California, UsAs the Strategy Lead for Clinical Quality Assurance & Risk Management, my standout achievement has been the successful implementation of a robust Quality Management System (QMS) during the early development phase at gRED. Specializing in quality risk management, I've pioneered risk-based auditing and risk-based monitoring guidance. A significant milestone under my leadership was the creation of analytics for audit data, which has been instrumental in providing key metrics and KPIs for our annual report. These analytics have enhanced our understanding of compliance levels, risk profiles, and operational efficiencies. My initiatives have not only ensured adherence to Good Clinical Practice (GCP), Pharmacovigilance (PV), and Computer System Validation (CSV) but have also set new benchmarks for quality and risk management in the industry. -
Clinical Scientist | Regulatory Affairs Project ManagerNorthwestern University - The Feinberg School Of Medicine Dec 2006 - Dec 2008Chicago, Il, UsAs a Clinical Project Manager and Regulatory Liaison, I have extensive experience in transitioning projects from bench research to clinical stage, including specialized work in CD34 stem cell therapy for cardiovascular regenerative medicine and bench-side research in neurodegeneration. My role encompasses comprehensive oversight of project management, regulatory affairs, and clinical research, including IND submissions, protocol development, and the submission of annual and safety reports. My multidisciplinary expertise has been crucial in ensuring seamless transitions and compliance with industry and regulatory standards. My leadership has been key in meeting project milestones, navigating the complexities of regulatory submissions, and maintaining the integrity of clinical trials -
Clinical Project Manager & Sr. ResearcherTufts University School Of Medicine Jul 2004 - Dec 2006Boston, Ma, UsAs a Sr. Scientist, I've spearheaded clinical operations and regulatory affairs across a diverse portfolio of clinical programs. My leadership has been instrumental in advancing Phase I & II clinical trials in cardiovascular diseases such as CHF and CAD, as well as vascular diseases like CLI and PAD, leveraging cutting-edge Gene Therapy and Stem Cell research. In addition, my involvement in bench research for neurodegeneration has led to multiple publications in areas like Alzheimer's, Parkinson's, and Inclusion body myositis. My role has been pivotal in IND submissions, protocol development, and the submission of annual and safety reports, setting new benchmarks for clinical and regulatory excellence. -
Scientist - Metabolism And ToxicokineticsHelmholtzzentrum München Jan 2001 - Jul 2004Neuherberg, Bayern, DeAs a Scientist specializing in Metabolism and Toxicokinetics, I've been a key collaborator within a multidisciplinary research team, working closely with industry partners. My contributions have been groundbreaking in the field of high-throughput toxicokinetics, where I've been involved in both mathematical and experimental modeling. I've successfully generated and validated new models, setting new standards for accuracy and reliability in the field. My work has not only advanced our understanding of toxicokinetics but has also been recognized through co-authored research papers, underscoring my commitment to scientific excellence and collaborative research.
Vimal V. Skills
Vimal V. Education Details
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Northwestern UniversityMedical Clinical Sciences/Graduate Medical Studies -
Regulatory Affairs Professional SocietyPharmacy Administration And Pharmacy Policy And Regulatory Affairs
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University Of MadrasBiochemistry
Frequently Asked Questions about Vimal V.
What company does Vimal V. work for?
Vimal V. works for Innvocept Global Solutions
What is Vimal V.'s role at the current company?
Vimal V.'s current role is Chief Strategy Officer (CSO).
What is Vimal V.'s email address?
Vimal V.'s email address is ve****@****hoo.com
What schools did Vimal V. attend?
Vimal V. attended Northwestern University, Regulatory Affairs Professional Society, University Of Madras.
What are some of Vimal V.'s interests?
Vimal V. has interest in Science And Technology, Education, Economic Empowerment, Health.
What skills is Vimal V. known for?
Vimal V. has skills like Biotechnology, Clinical Development, Clinical Trials, Clinical Research, Gcp, Pharmaceutical Industry, Management, Life Sciences, Glp, Biochemistry, Oncology, Fda.
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