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Detail-oriented and highly organized Clinical Research Associate (CRA) with [X] years of experience in monitoring and managing clinical trials across multiple therapeutic areas. Skilled in ensuring compliance with ICH-GCP, FDA, EMA, and other regulatory guidelines, conducting site visits, and maintaining high-quality data integrity. Adept at site initiation, monitoring, and close-out activities, ensuring patient safety, and collaborating with investigators and site staff. Proficient in using electronic data capture (EDC) systems and resolving protocol deviations efficiently. Strong communication, problem-solving, and analytical skills, committed to delivering high-quality clinical research outcomes.

It is said that I am a curious ,inquistive and detailed person. I love change management, turnarounds and strategically fixing problems and fueling growth.
I aim to advance in fields such as bioanalysis and bioinformatics by improving myself in computer technologies over time.

Graduated from Binghamton University with a B.S in Pre- medicine with a concentration in Neuroscience. Passionate healthcare professional and dedicated customer service advocate with a rich background in patient care. I've built my career foundation as a Medical Assistant, gaining valuable experience at Summit Health and Binghamton University. My commitment to delivering excellent patient care extends beyond the workplace, driving me to make a positive impact in my community.

A US veteran and Clinical Research professional with over 7 years experience and a strong background in clinical research. I have demonstrated a strong work ethic, discipline, and commitment with attention to detail, adherence to protocols, and the ability to work in a team. I worked on diverse range of clinical trials, gaining valuable experience and my expertise extends to performing all types of on-site and remote site monitoring visits, including Pre-Study Visits (PSV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV). I have experience with both 100% Source Data Verification (SDV) as well as reduced SDV approaches. I am proficient working with various clinical and/or client-specific systems for trial management, such as Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS) and Interactive Web Response Systems (IWRS). My extensive experience, exceptional problem-solving skills, adaptability make me a highly capable and well-rounded professional in the dynamic and fast-paced environment of clinical research.

Anagha Tarade

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Clinical Research Associate

Intern

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Post-Graduate Diploma - Clinical Research And Pharmacovigilance

Bachelor of Pharmacy - Pharmacy

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Clinical Research Associate

Post-Graduate Diploma - Clinical Research And Pharmacovigilance

Intern

Bachelor of Pharmacy - Pharmacy

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