Randstadeos

Clinical Trial Feasibility Specialist

Posted Oct 25, 2024
Project ID: 6678887655
Location
Bangalore, karnatka
Hours/week
40 hrs/week
Application Deadline: Dec 27, 2024 5:43 PM

Who you are:

  • Bachelors degree in scientific or business area

  • 3+ years of clinical trial feasibility experience supporting data-driven decision making

  • Familiarity with relevant operational and feasibility data, applications, and systems used in the pharmaceutical industry

  • Excellent analytical and problem-solving skills

  • Solid organizational skills, high quality focus and result orientation

  • Advanced Excel and Powerpoint skills

  • Proactively addresses and manages risks and issue escalation

  • Ability to work on multiple projects simultaneously

  • Experience working with diverse cross-functional and international teams

  • Exceptional interpersonal skills, including ability to communicate clearly and actively contribute to team meetings

  • Fluency in English

 

Responsibilities

  • Research scientific/clinical information that may include but is not limited to: disease background, current standards of care, how the proposed intervention fits into the current and projected future treatment landscape, and competing therapeutics in clinical development.

  • Conduct data mining of internal and external databases for use in development of robust operational strategies for global clinical trials (country/site mix, site identification, enrollment scenario modeling.)

  • Use site intelligence and local cross-functional input for study-level operational planning and potential site list identification

  • Support consistency of deliverables and development of best practices

  • Identify, analyze, and describe the competing clinical trial landscape to assist in assessing trial feasibility

  • Maintain detailed records of work and create and maintain internal libraries and databases

  • Collate results of various analyses into a comprehensive, yet concise report, with tables, graphs and all cited references.

  • Participate in intra and inter-departmental meetings

  • Support development and evolution of ODC data and analytic capabilities to advance clinical trial operational planning and data-driven decision making

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