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IQVIA BSc Job For Life Sciences – Clin Process Associate Job

IQVIA BSc Job For Life Sciences – Clin Process Associate Job. Interested and eligible applicants can check out all of the details on the same below

Name of the Post – Clin Process Assoc

Primary Location – Thane, Maharashtra, India

Full time

Job ID – R1293391

JOB DESCRIPTION

Job Overview

Provide project-related assistance for all assigned project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.

Essential Functions

  • Perform processes and tasks that eventually result in high-quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
  • The task may be assigned to either Start-Up studies or Maintainance studies.
  • Establish and maintain effective project/ site communications
  • Create and maintain relevant project documents
  • Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project-specific information
  • Review, evaluate and recommend modifications to designated processes
  • Participate in document management (creation, review, maintenance, storage, as applicable)
  • Participate in (study) team meetings and implement action items
  • Collaborate with the project lead/team members in the creation/review of study documents
  • Setting quality standards and reviewing deliverables to the same for process tasks.
  • Work on visit tracking in CTMS for Investigator payments, Vendor Setup QC’s, PV Batch Review, Passthrough invoice Batch Review & associated tasks.
  • Providing and revoking access.
  • Review ATP (Authorization to proceed) training.
  • Coordinating with translation vendors.
  • Understanding the contracts & enabling excellent output quality for the processing teams.
  • Ensure effective and efficient coordination between the operations team (PM/RSU/Clinical/IPA) for visit/passthrough batch query resolutions.
  • Ability to work in a deadline-orientated environment and manage SLAs (TAT, Productivity, Quality) effectively.
  • Respond to ad-hoc requests for data/information/analysis.
  • Responsible for general administrative support for projects, tracking various kinds of activities.
  • Responsible for indexing.
  • May act as a buddy for new Hires and SMEs for the team

Qualifications

  • Bachelor’s Degree
  • Life Sciences graduates with a minimum of 2 years of relevant experience.
  • Good knowledge of, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines
  • Excellent excel skills with VBN knowledge
  • Strong analytical skills
  • Strong written and verbal communication skills including good command of the English language
  • Results and detail-oriented approach to work delivery and output
  • Good problem-solving skills
  • Good planning, time management and prioritization skills
  • Ability to handle conflicting priorities
  • Attention to detail and accuracy in work
  • Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  • Proven ability to work on multiple projects balancing competing priorities
  • Good leadership skills
  • Ability to work across cultures and geographies with high awareness and understanding of cultural differences.
  • Setting quality standards and reviewing deliverables to the same for process tasks.

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