Rasika Bhutekar

Experience

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  Grant Medical Foundation, Ruby Hall Clinic, Pune

  Sept 2014 - Jan 2015

  Intern

  1) feasibility assessments2) Protocol Preparation & Review3) Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.4) Assists PI in communication of study requirements to all individuals involved in the study. 5) Documents date of training and signatures of study personnel trained on study specific training log.6) Collects documents needed to initiate the study and submit to the sponsor (e.g., FDA Forms 1572, CVs, etc.).7) Works with the PI to develop and implement recruitment strategies in accordance with IRB requirements and approvals.8) Conducts or participates in the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study.9) Obtains appropriate signatures and dates on forms in appropriate places. 10) Coordinates participant tests and procedures. Show less

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  Inamdar Multispeciality Hosital

  Feb 2015 - Jun 2015

  Clinical Research Coordinator

  1. Handling all institutional study with all study requirement.2. Communication with CRO , CRA and with Principal Investigators 3. Also working as a Ethics committee staff .4. Coordinating EC submission 5. Conducting EC meeting6. Making Agenda of EC Meeting7. Protection of Human Right8. Compliance to ICH-GCP9. Review AE/SAE

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  Syntel

  Jun 2015 - now

  Senior Associate