Clinical Research Specialist

Há 15 horas

São Paulo, São Paulo, Brasil beBeeActivation Tempo inteiro R$120.000 - R$140.000
Job Overview

The Site Activation Specialist is responsible for executing site activation and maintenance activities in accordance with regulations, standard operating procedures, and project requirements at the regional or country level.

This role involves serving as a key point of contact for feasibility, site activation, and maintenance activities in assigned studies for investigative sites. The specialist reviews documents for completeness, consistency, and accuracy and prepares site documents, reviewing them for completeness and accuracy.

Key responsibilities include informing team members of completion of regulatory, contractual, and other documents for individual sites, distributing completed documents to sites and internal project team members, and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.

The Site Activation Specialist will also review, track, and follow up on the progress, approval, and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.

Responsibilities include:

  • Serving as key point of contact for feasibility, site activation, and some maintenance activities in assigned studies for investigative sites.
  • Reviewing documents for completeness, consistency, and accuracy.
  • Preparing site documents, reviewing them for completeness and accuracy.
  • Informing team members of completion of regulatory, contractual, and other documents for individual sites.
  • Distributing completed documents to sites and internal project team members.
  • Updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
Requirements

Qualifications include:

  • Bachelor's Degree in Life sciences or a related field.
  • 1-3 years' clinical research experience in the Site Activation/Regulatory and Start-Up team in a CRO environment.
  • Advanced level of English skills.
  • Excellent communication and teamwork skills.
Key Skills

Key skills for this role include advanced knowledge of clinical research, document management, and collaboration tools, as well as excellent analytical and problem-solving skills.

Benefits

This role offers opportunities for professional growth and development in a dynamic and innovative environment, with a focus on delivering high-quality results and exceeding customer expectations.

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