Tanaya Nalavade

Dedicated Clinical Research Coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices guidelines and IRB regulations. Practiced problem-solver with strong attention to detail.

Mentoring and guiding new hires (CRCs and RAs). Proven abilities in managing schedules, lab results and eCRFs and sources.

Proactive leader with strengths in communication and collaboration. Adept at managing concurrent objectives to promote efficiency and influence positive outcomes. Experience using various EDC platforms - Veeva vault, iMedidata, Realtime, Hibbert, Medable and regular use Longboat, IWRS, SIP, Firecrest etc.

Proficient in rapport building, handling patient information, laboratory samples and compliance procedures for multiple clinical trials at a time. Well-organized and hardworking with excellent communication and planning skills with strong sense of prioritization. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.

Pursuing full-time role that presents professional challenges and leverages interpersonal skills, effective time management, and problem-solving expertise. Thorough team contributor with strong organizational capabilities. Experienced in handling numerous projects at once while ensuring accuracy. Effective at prioritizing tasks and meeting deadlines.

Results-oriented achiever with proven ability to exceed targets and drive success in fast-paced environments. Combines strategic thinking with hands-on experience to deliver impactful solutions and enhance organizational performance.