Akshay Teli

Background

About Akshay Teli

PROFILE SUMMARY 3+ years of experience in clinical research profession as enthusiastic person with master’s in pharmacology, have commendable knowledge and experience in clinical Research, equipped with strong analytical and problem-solving skills.•Passionate individual with great interpersonal and communication skills. Seeking for more exciting and challenging opportunities in Clinical ResearchTo work in a Professional environment with a dynamic and positive attitude that would give me an opportunity to utilize my intellectual ability for betterment of my organisation.Currently working as ACM, Support CM subject lead for reviewing subject data entered in EDC and ensure subject safety.Review Medical history, Adverse events and Concomitant medications for clinical congruency and consistency throughout study cycle.If any discrepancy found raise query to site for clarification and corrections to data entered in eCRF.Protect safety and rights of participants in clinical trials.Exposure to sponsor Audit like Merck which strengthened my understanding of compliance and data quality expectations.Ensure site conduct trial as per Protocol, SOP and other regulatory requirements.Perform advanced data visualization and analytics tool to proactively identify risks.Experience in Risk Based Monitoring (RBM) in clinical trial operations and skill in aggregating datareview and interpretation using visualization tools and analysis software.Utilizing broad knowledge of clinical operational systems and practices gained through extensiveexperience and education, implementing this to enhance study processes and outcomes. In my previous CMA role coordinating with project teams in system access skilled with Account Reconciliation, Access management, good communication skills. Strong understanding of site payment process and importance of timely site payments.Ensures Timeliness completeness and accuracy of documentation in TMFWorking with cross-functional study teams to administer document collection & storing foraudit.Handled more than 15 Projects which distributed among Start Up Phase, Maintenance Phaseand Close out Phase.Uploading Clinical documents in various TMF systemsManaging client and internal call Meeting minutes.Subject Matter Expert in Access Resource Management Group and as a mentor providing guidance, advice, feedback and support to the Mentee’sManaging various vendors EDC & IRT system access management to different stake holders andsponsors includes Site creation, User access management and Reconciliation process.