SR. CRA

ClinSync Clinical Research Pvt Ltd

are, conduct and report on activities related to the completion of site selection, initiation, routine monitoring and close-out visits

tor patient enrollment to ensure recruitment targets and project timelines are met at the site and/or country level

orm source data verification and follow up on data queries at the site level, on-going review of any Based Monitoring related information influencing data quality and frequency of site visits

re accurate and timely reporting and follow up of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations

as the main line of communication between the Sponsor and the site.

a point of contact/liaison for in-house support services and vendors.

re proper handling, accountability and reconciliation of all Investigational Product(s) and clinical study supplies

ew the status and contents of essential documents at the site level and reconcile study OSF/ TMF at site and/or country level.

rience in all types of monitoring visits.

• Experience

  6 - 10 Years

• No. of Openings

  2

• Education

  B.Pharma, M.Pharma, M.Sc

• Role

  Clinical Research Associate

• Industry Type

  Hospitals / Medical / Healthcare Equipments

• Gender

  [ Male / Female ]

• Job Country

  India

• Type of Job

  Full Time

• Work Location Type

  Work from Office