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DOCS CRA any level homebased in Brazil

CRA any level homebased

Ref #: 28267

Employment type: Permanent - Full-Time

Location: Brazil

Posted: 08-Apr-2021


Clinical Research Associate any level

The Role and your Responsibilities

The experienced field based / home based CRA (Clinical Research Associate) will perform all aspects of CRA work covering site evaluation, site initiation visits, site monitoring and close-out visits across phase II and phase III clinical trials in different medical indications.

CRA responsibilities:

  • Facilitate subject enrolment at the site level with focused patient recruitment strategies and action plans;

•* Identify site needs and site-related issues, escalate and/or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process;

  • Respond to site-related queries and escalate site-related issues with operational site management responsibility;

•* Perform investigational product accountability and reconciliation, maintain site study supplies, and facilitate the resolution of clinical queries to investigative staff;

•* Build and maintain solid and long-term professional relationships with investigators and site staff;

•* Ensure clinical study sites are conducting clinical trials in compliance with the respective protocol, our client's SOPs and applicable ICH/GCP guidelines and regulations;

  • Assist in preparing sites for audits, review audit reports and contribute to resolving findings;

•* Implement new technologies and systems at clinical sites, e.g. EDC systems;

  • Ensure appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAEs) and to verify case reports and source documentation;

•* Input and maintain electronic site management systems, provide input into clinical monitoring plans, input into case report forms and study-related documents as requested.

What is Offered

As a field-based/home-based CRA, you will have the opportunity to work with a sought-after client’s clinical trials in phase I-IV across different therapeutic areas. Our client is looking to recruit motivated and dedicated CRAs at all levels (Clinical Research Associate) in various regions

  • Permanent and full-time contract of employment seconded to our client

  • Home-based working

  • Salary according to actual level of skills and experience

  • Company benefits to include generous annual leave plus bank holidays etc

  • Fully structured 4-week training for all new starters

What is Required

  • Previous CRA experience of commercial phase II and phase III studies

  • Proven external/independent clinical trial monitoring experience gained in the country

  • Life science degree (BSc) o RN (registered nursing qualification)

•* Full working eligibility

•* Ability to work effectively within fast-paced working environments


DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.