Uma Chandrasekaran

WORK HISTORY

EDUCATION

ABOUT UMA CHANDRASEKARAN

QUALIFICATIONS HIGHLIGHTS:• Sucessful global clinical development, medical affairs, and program management experience.• Trusted and dependable as a medical and clinical affairs leader with product launch and first-patient-in experience• Expertise in analyzing and utilizing Real World Data to generate Integrated Evidence Plans. • Experienced in directing and implementing global publication and scientific communication strategies.• Successful in leading the execution of medical and clinical knowledge transfer across multiple functions.• Seasoned in managing medical affairs initiatives including leading advisory boards and patient-centered activities.• Demonstrated ability to partner with key opinion leaders and cross-functional members to deliver results.• Adept at understanding the competitive landscape, clinical practice trends, and emerging scientific advances. • Well-versed in effectively communicating complex clinical concepts via omni-channel engagement activities.• Skilled in leading global sponsor led and investigator initiated phase I-IV clinical trials and non-interventional studies.• Accomplished in program management across therapeutics with expertise in oncology, immunology, and cardiology.• Knowledgeable on all aspects of clinical protocol development, regulatory documents, and manuscripts.• Subject matter expertise in evaluation of technologies aiding business development efforts.• Well-versed in global regulatory requirements as well as ICH and GCP guidelines ensuring full regulatory compliance.• Skilled in managing multiple concurrent project deliverables, timelines, budgets, and reporting.• Strong program management acumen with exceptional planning, communication, and relationship building skills. • Ability to adapt and make informed decisions in ambiguity, and to advocate and influence at different levels.• Results-driven, strategic, analytical, collaborative, passionate, and a creative problem solver.KEY COMPETENCIES:Clinical Development • Medical Affairs • Program Management • Project ManagementBudget Management • Regulatory Compliance • Cross-Functional Leadership • Stakeholder ManagementKOL Management • Advisory Boards • Investigator Initiated Trials • Sponsored Clinical Studies Integrated Evidence Plans • Lifecycle Management Plans • Real World Data Analysis • Artificial IntelligenceData Analysis • Systematic Literature Reviews • Medical Writing • Scientific CommunicationsInnovative Study Design • Protocol Writing • ICF/CRF/IB Writing • ICH/GCP Guidelines