Your browser does not support javascript! Please enable it, otherwise web will not work for you.

Join Clinical Research Courses and 100% job Assistance!

Chat




Centralized Trip Report Reviewer

Home > IT Jobs

Centralized Trip Report Reviewer in Bengaluru-Karnataka new

  • MICR0LABS
  • Full time
  • Email
  • Bengaluru-Karnataka
  • 2024/05/10
  • Report

Centralized Trip Report Reviewer #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharmaindustry #doctor #phd #oncology #drugdevelopment #cra #biotechnology # Management of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Covance Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation of Initiatives either independently or with team) Proactively identify opportunities for process improvements and work collaboratively with project team incase further action required Complete required trainings according to required timelines. Follow applicable departmental Standard Operating Procedures and Work Instructions Follow project issue escalation process and Covance Corrective Action Issue Resolution (CAIR) process for clinical operations issues Ensure follow up on issues and risks and protocol deviations and to be a liaison between CRA, CTL and PM for timely resolution of issues Responsible for the timely and appropriate communication to the clinical operations team Liaise with CTL/PM to communicate any trends, outstanding issues, safety concerns or any other activity or lack thereof which may jeopardize the clinical trial delivery or patient safety. Review progress of project and initiate appropriate actions to achieve target objectives assigned. Support in review of Standard Operating Procedures or Work Instructions to align with process or tool modifications Other duties as assigned by management: Ex: Document Review, ETMF reconciliation, other CTL tasks etc.

₹ 3,50,000 - 4,75,000 P.A.



MICR0LABS

Micro Labs Limited emerges as a preeminent technology-driven healthcare entity, recognized for its cutting-edge Research and Development (R&D) and state-of-the-art automation-driven manufacturing facilities. The company consistently excels in international regulatory audits, reinforcing its commitme...

Similar positions

SVRR - Site Visit Report Review

  • covance by labcorp
  • Full time
  • Gurgaon-Haryana
  • 2024/05/10

8 lakhs to 12 lakhs per annum

Medical Data Reviewer

  • Quanticate
  • Full time
  • Kochi-Kerala
  • 2024/05/10

6.54 lakhs to 12 lakhs per annum

Medical Reviewer

  • Labcorp
  • Full time
  • Bengaluru-Karnataka
  • 2024/05/10

5.3 TO 6.8 LPA

Medical Writer and Reviewer

  • Mercury Mentors
  • Full time
  • Bengaluru-Karnataka
  • 2024/05/10

₹ 1,75,000 - 3,25,000 P.A.

QC Reviewer

  • IQVIA
  • Full time
  • Chennai-TamilNadu
  • 2024/05/10

9 lakhs to 12 lakhs per annum