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ICON plc Hiring Clinical Research Associate In Bangalore location, minimum Qualification is Bachelor degree in Science or Pharmacy

Icon Clinical Research Job vacancies details mentioned below

Company Name – ICON plc

Post Tittle – Clinical Research Associate

Location – Bangalore Urban, Karnataka, India (On-site)


QUALIFICATIONS:

Bachelor degree in Science or Pharmacy with relevant knowledge in Clinical Research.

Knowledge of ICH GCP and local regulatory authority regulations regarding drug.

Job Description

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPS), ICH-GCP, and all applicable regulatory requirements.


Requirements:

Demonstrates excellent written and oral communication.

Demonstrates excellent knowledge of ICH/GCP

Displays ability to manage investigative sites to
facilitate trial deliverables

Demonstrates ability to escalate issues appropriately

Conducts monitoring to confirm subject safety and data integrity

Describes and demonstrates the principals of IP accountability

Identifies scientific misconduct at the site level

Demonstrates working knowledge of Microsoft applications, Clinical Trial Management Systems (CTMS), Office IVRS/IWRS and Electronic Data Capture (EDC) platform

Mentors CRAS new to the position or company

Serves as an observation visit leader.

Conducts monitoring evaluation visits.

Assists team lead in the development of trial tools or documents


(Responsibilities):

Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines

▪ Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites

▪ Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely

▪ Provides regular site status information to team members, trial management, and updates trial management tools

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Application Link Click below

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