Meghana Guddehithlu Vishweshwara Email & Phone Number

Munich, Bavaria, Germany

Eager to channel my passion for data-driven insights into the dynamic field of Clinical Research. Currently expanding my skill set by learning the SAS, I am committed to staying at the forefront of industry advancements. With a background in Clinical data management, I bring a strong foundation in data management principles and a keen eye for detail. I am excited about the prospect of leveraging my expertise and embracing new challenges in the clinical research arena

Munich, Bavaria, Germany

Transitioning from a bustling career to full-time parenting for six months provided invaluable insights into nurturing and family dynamics. Following this enriching experience, I embarked on a relocation journey to Munich, Germany, in support of my spouse's career aspirations. During this phase, I seized the opportunity to update my skills, completing Project Management certification from Google and delving into Clinical Trial Management courses from Johns Hopkins University. Additionally, I've… Show more Transitioning from a bustling career to full-time parenting for six months provided invaluable insights into nurturing and family dynamics. Following this enriching experience, I embarked on a relocation journey to Munich, Germany, in support of my spouse's career aspirations. During this phase, I seized the opportunity to update my skills, completing Project Management certification from Google and delving into Clinical Trial Management courses from Johns Hopkins University. Additionally, I've been immersing myself in learning the German language to embrace the local culture fully. Eager to apply my refreshed skills and global perspective, I look forward to new opportunities and connections in Munich's vibrant professional landscape Show less

Bengaluru, Karnataka, India

Passionate Data Operations Coordinator with a proven track record of leading teams and ensuring seamless collaboration in the execution of Phase 1 & Phase 3 clinical trials within the Oncology therapeutic area. Skilled in managing Trial Master File (TMF) maintenance to ensure regulatory compliance throughout trials. Experienced in crafting project-specific documents, including data management plans and eCRF guidelines, contributing to project success. Proficient in managing data entry, testing,… Show more Passionate Data Operations Coordinator with a proven track record of leading teams and ensuring seamless collaboration in the execution of Phase 1 & Phase 3 clinical trials within the Oncology therapeutic area. Skilled in managing Trial Master File (TMF) maintenance to ensure regulatory compliance throughout trials. Experienced in crafting project-specific documents, including data management plans and eCRF guidelines, contributing to project success. Proficient in managing data entry, testing, validation processes, and reconciling external vendor data. Adept at generating statistics, status reports, final reports, and managing data queries. Committed to fostering inclusivity and growth, Show less

Experienced Clinical Data Manager proficient in managing Phase 1, Phase 3, and Phase 4 clinical trial studies across diverse therapeutic areas including Oncology, Cardiovascular, Respiratory, Diagnostic tools, Musculoskeletal, and Devices. Skilled in leading data review teams and overseeing all data review activities to ensure accuracy and completeness, contributing to study success. Adept at conducting user acceptance testing (UAT) of EDC systems, database design, programming of data entry… Show more Experienced Clinical Data Manager proficient in managing Phase 1, Phase 3, and Phase 4 clinical trial studies across diverse therapeutic areas including Oncology, Cardiovascular, Respiratory, Diagnostic tools, Musculoskeletal, and Devices. Skilled in leading data review teams and overseeing all data review activities to ensure accuracy and completeness, contributing to study success. Adept at conducting user acceptance testing (UAT) of EDC systems, database design, programming of data entry masks and edit checks, and drafting eCRF completion guidelines for optimized data capture efficiency. Proven track record in handling SAE reconciliation, developing data management plans, implementing quality control measures, and generating crucial study-related metrics and reports. Strong mentorship abilities, collaborating effectively with stakeholders to ensure the smooth continuation of clinical trials. Experienced in working with Electronic Data Capture (EDC) systems including Medidata Rave, iMednet, and IBM eCOS. Show less