Santosh Shevade Email & Phone Number

Mumbai, Mh, In

-Led developing, designing and finalizing several successful grant and funding proposals-Presented the work of REAN Foundation at the conclave by Indian Association of Preventive and Social Medicine at Dayanand Medical College & Hospital on ‘Community-Driven Innovation in Open-Source Digital Health: Advancing Integrated Care Delivery’.-Served on the jury at the TiE’s TiE Global Summit University PitchFest. It was an excellent event where we reviewed diverse ideas ranging from regenerative medicine to aeronautics capabilities-Engage REAN program product teams to embed methods to measure outcomes and impact into the solutions across the prototype, pilot and implementation phases-Develop partnerships with healthcare organizations and other non-profits and cultivate strategic relationships with key partners

Leading and supporting solution architecture for projects with a Big Pharma client-covering aspects including exploring data sources, providing domain expertise, solution creation, testing and validation

Working with Saathealth team in delineating data sciences strategy to use scientific methods to extract meaningful insights from health data

Deep-dive sessions on biopharma and its role in the healthcare delivery system

Mumbai, Maharashtra, India

3 Credit course on Information Technology in Healthcare

Mumbai Metropolitan Region

I work with healthcare firms, health technology start-ups, incubator/accelerator set-ups, and hospitals on diverse projects ranging from corporate innovation journeys, start-up mentoring on idea validation, outcomes research and implementation, and project leadership/management.Key projects--Advisor for design and implementation of a digital platform influencing behaviors and health outcomes for healthcare consumers-Design, development and project management of care continuum pathway using a technology assisted solution in non-communicable diseases-Conceptualizing and designing clinical trial recruitment platform using data analytics-Conceptualizing and designing outcomes trial for a mHealth based intervention to assess uptake and impact as compared to standard of care

-DiMe Research Committee Member for Apr 2021-Apr 2023-leading research projects to advance digital medicine-Partnering with DiMe Society for driving adoption of 'The Playbook'-essential industry guide for successfully developing & deploying digital clinical measures across clinical research, clinical care, and public health

Remote

KidsX is an international consortium of pediatric hospitals focused on improving digital health innovation through collaboration. Led by the Innovation Studio at Children's Hospital Los Angeles (CHLA), KidsX facilitates relationships between leading children’s hospitals and entrepreneurial innovators to build, test and deploy software solutions to make pediatric care exceptionally effective, safe, efficient and convenient for children and families

Hyderabad Area, India

Established a healthcare innovation management consultancy, focusing on impact/outcomes management for healthcare innovation interventions, capability build in healthcare innovation practices and ecosystem.Key Results-Supported impact assessment and reporting of a mHealth intervention in AIDS knowledge dissemination and treatment literacy for a UK based start-up-Successfully conceptualized and implemented hands-on 'Applied Innovation' workshop for scientists at Indian Council for Medical Research discussing technology readiness, technology transfer and other areas of application oriented healthcare research-Designed and implemented domain mentoring for HealthTech start-ups at IIIT-Hyderabad, taking them through idea validation, GTM strategies, immersions and journey mapping using a design thinking approach-Consulted with two pharmaceutical organizations in identifying digital touchpoints for their commercial teams

Hyderabad Area, India

I was the global head of the ~100 clinical scientists working on Novartis Global Drug Development (GDD) studies towards clinical excellence in study design, data review and reporting.Over the 1.5 years in the role, I continued in the hiring and talent management for the group, by growing the team by about 40% in number and supporting approximately 60% more work. I successfully provided oversight in getting the group support newer therapeutic areas, including Novartis Oncology studies as well as take up additional functional deliverables like study document writing and clinical reviews.As part of the Novartis India GDD Leadership team and contributed to several Hyderabad level initiatives including leading a working group defining GDD talent strategy.Due to my interest in leadership development, I was also a facilitator for Novartis First Line Leadership training; Over the course of 2 years, I delivered a total of 6 sessions, helping ~150 Novartis people managers and matrix leaders learn and practice several management and leadership skills.

Hyderabad Area, India

-Established a Clinical Data Review ‘Center of Excellence’ by hiring and managing a team of ~30 skilled clinical scientists in Neuroscience and Retina franchises in Hyderabad and Dublin-Led Novartis Pharma Development global workstreams on streamlining data review process for clinical trials by managing a cross-functional team of associates-Co-led two global work-streams on global process improvement on resourcing and team dynamics, leading to streamlined resource decisions and improved productivity through high-performing teams.-As part of the Novartis India Pharma Leadership team, led 'Best Place to Work Initiative'-a cross-functional team in organizational development of Novartis Hyderabad site.

Hyderabad Area, India

Responsible for global trial management of Phase 3 submission trials, including trial planning and risk management, country start-up and regulatory processes, training countries and sites, recruitment planning and management, vendor and database management, clinical data review and resolution of issues.-Managed key clinical submission activities for a large Phase 3 program, to manage complex lab sample workflows across 6 PhII trials, QC of TMF documentation across 16 PhIII trials and protocol deviation listings across 5 PhIII trials-Active contribution to resourcing algorithm workstream for the Global Clinical Trial Management organization-Led rollout and conduct of advanced Good Clinical Practices program across the Novartis Hyderabad site managing a team of 20 training facilitators, covering more than 600 associates; Was awarded global Training Hero award by Global Quality Function.

Hyderabad Area, India

Responsible for global trial management of Phase 3 submission trials, including protocol development and writing, trial planning and risk management, country start-up and regulatory processes, training countries and sites, recruitment planning and management, vendor and database management, clinical data review and resolution of issues.

Mumbai Area, India

- Recruited to help the startup activities and management of newly established centralized clinical operations unit in JJPRD, systems and programs. - Worked with country management to establish clinical trial processes and procedures; end to end trial management experience including planning and resourcing, site and monitor training, oversight on ongoing trial activities and monitoring, close out activities, quality and risk management; recruit and develop employees; providing oversight to outsourced and medical affairs studies; - Currently responsible for portfolio management of Cardiovascular, Immunology, Medical Affairs Operations, people management in GCO India as well as oversight on clinical R&D trials and medical affairs trials in GCO Philippines; Part of the GCO India management team

Mumbai Area, India

Clinical Trial Management activities including Project Kick off, Planning and Start-up, Training Site teams and monitors, Ongoing trial oversight, close out activitiesPerformance Management of monitors

Mumbai Area, India

After 2 years of monitoring activities encompassing site selection, ongoing monitoring and close outs on Pfizer trials, was promoted to manage the regional monitoring structure in the regional monitoring group

Masters, Pharmaceutical Sciences

Pharmaceutical Chemistry

Bachelor, Pharmaceutical Sciences

Graduation in Pharmaceutical Sciences