Sr. CRA

ClinSync Clinical Research Pvt Ltd

6 - 10 Years
2 Openings
6.0-10.0 Lac/Yr
Hyderabad

Key Skills

Clinical Research Associate Event Management

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Job Description

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

About ClinSync Clinical Research Pvt Ltd

ClinSync has brought together under a common umbrella people with a depth and breadth of vision and thinking and with interests ranging from preclinical up to late stage trials aiding research into NCEs. While each of our people has a unique set of interests and needs, we all bring a strong result orientation, sense of urgency and ambition to make a positive difference to our client's businesses.