Icon Clinical Research Associate Job Openings For All Lifesciences Candidates » PHARMA STUFF
Search
Generic filters
Filter by Categories

Try these: FresherPharmacovigilanceMedical coding

Icon Clinical Research Associate Job openings for all Lifesciences Candidates

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 – 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

Experience

  • Degree, Masters or PhD in Life Science, Nursing or Health Related
  • Approximately, 2~ 4 years experience as a CRA (level 2 and 3) and special knowledge in a therapeutic area
  • Strong knowledge of ICH-GCP and a strong interest in clinical research
  • Professional use of the English language; both written and oral
20211023 135046 Icon Clinical Research Associate Job openings for all Lifesciences Candidates
Icon Clinical Research Associate Job openings for all Lifesciences Candidates 4
Scroll to Top
 
               Join Whatsapp Groups