Clinical Research Associate III

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Job title: Clinical Research Associate III

Company: Allucent

Job description: Job Description:

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment.

Ensures that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP) and International Conference on Harmonization (ICH).

Requirements:

  • Performs Selection, Initiation, Monitoring and Closure Visits at Investigator Sites according to project schedule. Adheres to project guidelines and POI SOPs for monitoring requirements.
  • Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols.
  • Tracks and supervises collection of ongoing study data for purpose of regular project status reporting.
  • Collects and reviews regulatory documents as required.
  • Prepares site visit reports and telephone contact reports.
  • May participate in the start-up process including reviewing protocols, reviewing CRFs, preparing Informed Consent forms, developing study documents, and organizing and presenting at investigator meetings.
  • Resolves site issues, including site recruitment challenges, and determines status for IP shipment.
  • Assists the Project Manager (PM), Clinical Team Leader and/or Lead CRA (CTL/LCRA) with generation of study specific forms for completion by CRA and Investigators and follow up with the teams to ensure timely completion and submission.
  • Works with PM/CTL/LCRA to secure authorization of site contracts.
  • Informs team members of completion of regulatory and contractual documents for individual sites.
  • Attends Investigator Meetings (IM) and study specific training meetings.
  • May translate, coordinate translations or review completed translations of critical documents.
  • Participates in feasibility and/or site identification activities. Contacts local opinion leaders, medical consultants or specified investigators and identifies sites with the potential for participation. Follows the feasibility procedures for documentation of feasibilities performed.
  • Identifies the documentation required for review by Regulatory Authorities and Ethical Committees. Prepare Regulatory and Ethics Committee submissions. Ensure written approvals are obtained and distributed appropriately prior to Site Initiation.
  • Prepares and attends an Assessment Visit with a more senior CRA, CTL or Clinical Research Manager as required.
  • Conducts Assessment and/or Training Visits of CRA I/II as required.
  • Assists the Project Team with the day-to-day management of critical studies as required, including attendance at team meetings.
  • Organizes processes for interim and final payments to Investigators, including preliminary calculations, review and approval from Project Management, liaison with POI accountant, logging trial expenditure, receipts, invoices and income.
  • Provides secondary in-house review of CRFs (if required).
  • Must work both independently and in a team environment.

Expected salary:

Location: Bangalore, Karnataka

Job date: Tue, 27 Sep 2022 22:54:31 GMT

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