Parth Mistry Email & Phone Number

Ahmedabad, Gujarat, India

Ahmedabad, Gujarat, India

Ahmedabad, Gujarat, India

Ahmedabad Area, India

• To review and clarify project data in accordance with the edit check plan.• To carry out query production.• To edit the database with answers to the data clarification forms (DCFs).• To enter data from case report forms (CRFs) and questionnaires and other project related documents as per data entry conventions of Clinical Data Management as assigned.• To edit the database for correction of data entry errors.• To run programs for double data entry comparison, listing of individual data, edit checks.• To perform Case Report Form (CRF) and DCF tracking.• To assist in the set-up, testing, and maintaining of the project database and the definition of data entry conventions.• To assist clinical data manager and senior clinical data manager in data management activities and other tasks as delegated..• To assist data entry coordinator(s) on how to enter the data, to supervise the data entry, to perform one of the entries foreseen by the double data entry procedure if applicable to the project.• To assist in the preparation of the edit check plan, self evident corrections, data entry conventions and other applicable data management documents.• To assist in the development and validation of the programs for comparing double data entry, listing individual data and applying edit checks.• To assist Clinical Data Manager/ Project Data Manager in CRF designing• To file study documentation.• To identify, communicate and resolve data issues to Clinical Data Manager/ Project Data Manager on a timely manner.• To implement defined quality control procedures as per Data Management Plan• To implement or adhere to SOP / regulatory requirements.• To liaise with other project team members.• To record all activities accurately on the company standard timesheet.

Ahmedabad Area, India

Working as Clinical Research Lecturer. I have been teaching topics like Clinical operation and CDM to my students and guiding them for Jobs too.

Ahmedabad Area, India

• eCRF Designing.• Database Setup.• Data Validation.

Ahmedabad Area, India

• Submitting regulatory documents to IRB and Sponsor• Submitting the clinical study agreement to OSP for review• Attending investigator meeting• Developing a preliminary budget and verify all costs• Helping PI negotiate the study budget direct costs with sponsor to cover all costs (F&A costs are not negotiable)• Preparing for study initiation• Obtaining physician signatures• Recruiting subjects• Screening and scheduling subjects• Getting voluntary subject consent• Teaching subjects about protocol expectations for them• Performing study/protocol procedures in a detailed, accurate manner• 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• treatment• resolution• Processing and shipping lab work• Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel, including: IRB Office of Sponsored Projects Research Accounting• Completing case report forms (CRA) for PI review and approval• Helping study monitors with CRA corrections • Maintaining study-specific supplies• Preparing for study closure and archiving

Bachelor Of Pharmacy - Bpharm

Bachelor’S Degree, Pharmacology, 6.9 Cgpi

Activities and Societies: • Participated in Science Carnival in 2013. • Collected award in Cricket tournament in college. Studied Pharmacy

High School, Higher Education/Higher Education Administration, 64%

Activities and Societies: • Participated in 17th National Children’s Science Congress in 2009. • Collected award in Gujarat state art.