Clinical Research Associate I or II (BB-E826B)
Encontrado en: Expertini Argentina
Descripción:Clinical Research Associate I or II
**Ref #:** 25427
**Employment type:** Permanent - Full-Time
**Location:** Buenos Aires, Argentina - homebased
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 clients 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.
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.
calendar_todayhace 1 mes
info De jornada completa
location_onBuenos Aires, Argentina