Descripción:

Clinical Research Associate I or II


**Ref #:** 25427


**Employment type:** Permanent - Full-Time


**Location:** Buenos Aires, Argentina - homebased


**Posted:** 26-Nov-2020


**Description**


Clinical Research Associate Senior required

• Strong phase II/III commercial clinical monitoring experience with willingness to travel nation-wide.

• Excellent communication and time management skills to manage multiple projects at any one time.

• Being a strong team member who understands the need for effective communication at all levels.

• Ability to demonstrate effective relationship building with sponsors, sites and colleagues, as well as strong management skills

• Life science degree and clean full driving licence


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 Argentina


* Home-based working

* Very competitive salary

* Company benefits to include generous annual leave

* Fully structured 4-week training for all new starters


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 Required

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

• Proven external/independent clinical trial monitoring experience

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

• Full working eligibility

• Able 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.

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