Nirali Chauhan Email & Phone Number

Valsad, Gj, In

Vapi, Gujarat, India

Vapi

Ahmedabad Area, India

• Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.• Coordinates approval of new study agreements and contracts.• Performing study/protocol procedures in a detailed, accurate mannerPreparing for study initiation• Obtaining physician signatures• Participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols open to… Show more • Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.• Coordinates approval of new study agreements and contracts.• Performing study/protocol procedures in a detailed, accurate mannerPreparing for study initiation• Obtaining physician signatures• Participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols open to enrollment. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process• Coordinates with PIs and department to help ensure that clinical research and related activities are performed in accordance with GCP.• Recruiting subjects• Screening and scheduling subjects• Maintaining study files• Tracking and maintaining the study budget and payments, including invoicing the sponsor for completed work• Tracking subjects, avoiding lost-to-follow-up• Documenting an adverse event, including:describing the event,severity and frequency,treatments,resolution• Processing and shipping lab work• Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel• Completing case report forms (CRF) for PI review and approval• Maintaining study-specific supplies• Preparing for study closure and archiving• Arranges secure storage of study documents that will be maintained according to institutional policy• Promotes the ethical conduct of research by reporting good faith suspicions of misconduct in research as defined within the declaration of Helsinki. Show less

M.Pharma, Clinical Pharmacy

Bachelor Of Pharmacy (Bpharm), Pharmacy, First Class