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Cra I / Cra Ii / Cra Iii / Sr Cra

Intrials Clinical Research

Rio Branco

Híbrido

BRL 80.000 - 120.000

Tempo integral

Hoje
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Resumo da oferta

A leading clinical research organization in Brazil is seeking dedicated Clinical Research Associates (CRA I, II, III) to join their team. The role involves ensuring clinical studies are conducted following ICH-GCP guidelines and managing relationships with study sites. Candidates should have degrees in Health Sciences, relevant experience depending on CRA level, and excellent organizational skills. The company promotes a diverse and inclusive environment and offers a hybrid work model.

Qualificações

  • Degree in Health Sciences or equivalent.
  • Previous experience in clinical research for CRA I.
  • At least 2 years of experience in clinical research for CRA II.
  • At least 4 years of experience in clinical research for CRA III.
  • Knowledge of ICH-GCP and guidelines.
  • Excellent organizational and interpersonal skills.
  • Available to travel.

Responsabilidades

  • Ensure study is conducted according to ICH-GCP and regulations.
  • Ensure accuracy and verifiability of study data.
  • Perform monitoring activities and visits.
  • Act as primary contact for study sites.
  • Support PM and coach less experienced CRAs.

Conhecimentos

Organizational abilities
Interpersonal skills
Problem-solving orientation
Advanced English
Basic Spanish

Formação académica

Degree in Health Sciences or equivalent

Ferramentas

Microsoft Office tools
Descrição da oferta de emprego

CRA I / CRA II / SR CRA

Location : Brazil

Hybrid

Who We Are

Intrials is a disruptive company with all the attributes that a CRO must master. We mix innovative projects with the necessary skills to provide a full service. Nothing stops us in the search for knowledge. Transforming people's lives through science when it comes to solving the challenges of our clients' projects in a focused and exclusive fashion.

Diversity & Inclusion are essential to continue building our history of innovation. Diversity of color, belief, sexual orientation, religion, or any other characteristic are very welcome in all open positions at our company. It is a fundamental part of Intrials to constantly think and implement actions that reinforce the importance of good coexistence with all the people who are part of our DNA and together, to leverage and build true impactful results in our society.

Basic Functions and Responsibilities includes, but are not limited to :
  • Ensure that the clinical study is conducted according to the ICH-GCP guidelines, the local and international regulations as well as according to Intrials or Sponsor’s SOPs.
  • Ensure that clinical study data are accurate and verifiable.
  • Identify and perform the corresponding quality controls on source documents.
  • Perform monitoring activities and visits (on-site and / or remote): Site Selection Visit (SSV), Site Initiation Visits (SIV), Interim Monitoring Visit (IMV) and Close-out Visit (COV).
  • Participate in meetings / teleconferences with Sponsor and PM.
  • Act as main point of contact for study sites.
  • Provide support to PM and more experienced CRAs in the study coordination activities, as applicable.
  • Perform coaching activities for less experienced CRAs.
What you need :
  • Degree in Health Sciences or equivalent (Pharmacy, Biology, Biomedicine, Nursing, other).
  • For CRA I: Previous exp. in clinical research as CRA / CTA / Study Coordinator / In-House CRA at CRO, pharmaceutical company.
  • For CRA II: Reliable academic background and at least 2 years of experience in clinical research as a CRA at CRO, or pharmaceutical company.
  • For CRA III: Reliable academic background and at least 04 years of experience in clinical as a CRA at CRO, or pharmaceutical company.
  • Excellent organizational abilities and interpersonal relationships; oriented to solve problems; self-confidence.
  • Available to travel considerably and ability to manage travel schedules.
  • Knowledge of ICH-GCP, local and international guidelines.
  • Computer skills on Windows environment and Microsoft Office tools.
  • Advanced knowledge of English.
  • Basic Spanish is recommended (only applicable for CRAs from Brazil).
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