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Job highlights

Work/Life Balance

Time management

Flexibility

Problem Solving

Are you looking for an exciting opportunity in clinical research? ICON plc, a global leader in healthcare intelligence and clinical research, is looking for a Clinical Trial Assistant to join its dynamic team in Bangalore. If you’re passionate about advancing clinical trials and contributing to innovative healthcare solutions, this role is for you!

About ICON plc

ICON plc is a world-renowned organization in healthcare intelligence and clinical research, committed to delivering excellence and innovation. The company fosters a diverse and inclusive environment that allows for personal and professional growth. By joining ICON, you’ll be part of a team dedicated to shaping the future of clinical development.

Responsibilities as a Clinical Trial Assistant

As a Clinical Trial Assistant, you will have a crucial role in ensuring the smooth running of clinical trials. Your key responsibilities will include:

  • Keeping up to date with ICH GCP knowledge and operational procedures.
  • Supporting multiple clinical studies and prioritizing tasks to meet deadlines.
  • Maintaining study trackers, analyzing reports, and distributing dashboards to study teams.
  • Providing clinical administrative support for both In-house and FSO trials.
  • Managing study systems like eTMF, CSAP, and CTMS.
  • Collaborating with SDS/SM to manage activities post-SAC till final archival.
  • Ensuring TMF Management and Maintenance, improving compliance with timely follow-ups.

This role requires a high level of organization and attention to detail to ensure that all tasks are completed on time and in accordance with quality guidelines.

Required Qualifications & Skills

To be successful in this role, the following qualifications and skills are essential:

  • Technical/IT skills: Ability to understand the impact of technology on clinical trials and proficiency in using study management systems.
  • Knowledge of ICH GCP: Familiarity with Good Clinical Practice, relevant operational procedures, and quality guidelines for clinical studies.
  • Teamwork & Independence: Ability to work independently and as part of a team.
  • Communication: Excellent communication skills to coordinate with stakeholders and study teams.
  • Time Management: Ability to manage multiple tasks and meet deadlines for system updates, TMF activities, and reports.
  • Experience: 1-2 years of prior experience in clinical operations.

Benefits of Working at ICON

ICON recognizes the importance of its employees and offers a competitive salary along with numerous benefits designed to support well-being and work-life balance. Some of the benefits include:

  • Annual leave entitlements to enjoy your personal time.
  • A variety of health insurance plans to suit you and your family.
  • Retirement planning offerings to secure your future.
  • Access to the Global Employee Assistance Programme for 24/7 well-being support.
  • Life assurance and flexible benefits tailored to your country, including childcare vouchers, gym memberships, and more.

Application Link

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