Having earned his bachelor of science in zoology at North Carolina State University, Devansh Parikh manages a busy Fayetteville doctor’s office. He is responsible for interfacing with healthcare and insurance providers and ensuring the group's operational efficiency. In his secretarial position, Devansh Parikh also handles the practice’s patient database and manages day-to-day billing activities.
Mr. Parikh’s experience extends to engaging as a biology lab assistant while an undergraduate where he assisted in the preparation of Internet-based class modules. He subsequently served as a lab technician and provided a North Carolina State University resident research scientist with support in the development of a novel anti-cancer drug. His responsibilities included employing a variety of feeding strategies designed to boost protein production. He also undertook daily culture analysis that encompassed cell counts and variability sampling.
Mr. Parikh has nearly two years of experience with Shreenath Clinical Services in Yorba Linda, California, as clinical research coordinator. Here Devansh Parikh was tasked with maintaining updated regulatory binders covering clinical trials and facilitating the informed consent procedure for subjects of clinical trials.
Mr. Parikh’s experience extends to engaging as a biology lab assistant while an undergraduate where he assisted in the preparation of Internet-based class modules. He subsequently served as a lab technician and provided a North Carolina State University resident research scientist with support in the development of a novel anti-cancer drug. His responsibilities included employing a variety of feeding strategies designed to boost protein production. He also undertook daily culture analysis that encompassed cell counts and variability sampling.
Mr. Parikh has nearly two years of experience with Shreenath Clinical Services in Yorba Linda, California, as clinical research coordinator. Here Devansh Parikh was tasked with maintaining updated regulatory binders covering clinical trials and facilitating the informed consent procedure for subjects of clinical trials.
