Site Activation Specialist

hace 4 semanas


Xico, México Iqvia A tiempo completo
Job Overview

As a Site Activation Specialist at Iqvia, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines.

May also include maintenance activities. This role involves developing a professional individual contributor who works under moderate oversight and supervision. You will be responsible for making recommendations for enhancements in systems and processes to solve problems or improve the effectiveness of your job area. Problems faced are general and may require understanding of broader sets of issues but are not complex.


Essential Functions

  • Work with clinical study teams to ensure the accuracy of data in CTMS.
  • Provide support, under the direction of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist, to clinical systems end users, including receipt, evaluation, and recommendation for all issue/enhancement requests.
  • Conduct research and data analysis to identify potential sites that meet the study criteria and objectives.
  • Assist with feasibility launch to include system setup, feasibility questionnaire creation, and site-level feasibility questionnaire outreach.
  • Effectively communicate with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities.
  • Track and data entry of feasibility responses and report responses to internal stakeholders.
  • Troubleshoot any issues or discrepancies that arise in the feasibility process (in-house and/or outsourced studies).
  • Stay up-to-date with current regulations and industry trends related to site feasibility.

Qualifications

  • Bachelor's Degree in a Life Science or Scientific Health Field.
  • 3 years of clinical research experience conducting clinical trials and processes, preferably with North America (sites).
  • 2 years of feasibility and recruitment experience.
  • Experience with trial optimization vendors, tools, and methods.
  • Analytical thinker, attention to detail, and good communication skills.
  • Highly proficient with Excel.
  • Fluent communication in English.


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