Cra I (Xico)

Cra I (Xico)

20 ago
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Xico

20 ago

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Xico

ICON plc is a world-leading healthcare intelligence and clinical research organization.
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:
We are currently recruiting for a CRA in Mexico to work on a range of therapeutic areas for a prestigious and global biopharmaceutical company.
This particular CRA role is a client dedicated one where you will work exclusively on one sponsors trials and SOPs.
As a **Clinical Research Associate**, you will be dedicated to one of our global pharmaceutical clients, with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market.
Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.
- Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
- Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
- Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
- Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
- Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.
**You are**:




- Bachelor's Degree (or equivalent)
- A stable experience as a CRA, this within the pharmaceutical industry or a CRO
- Excellent organization skills
- ** Exp in RBM/RBQM** (Risk-Based Monitoring and Risk-Based Quality Management)
- Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
- Strong IT skills
- Strong communication with the ability to multitask and work effectively under pressure
- Experience conducting all types of MVs such as: Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site
- A demonstrated working knowledge of ICH/GCP Guidelines
- Fluency in Bulgarian and professional proficiency in English
**What ICON can offer you**:
Our success depends on the quality of our people.
That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits.
Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a general network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

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