Cra I - Barcelona, España - Labcorp

Labcorp

Empresa verificada

Barcelona, España

hace 4 días

Publicado por:

Isabel García

beBee Recruiter

Descripción

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries.

Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

Role Details:

We are recruiting for our sponsor-dedicated business in Spain and are currently seeking to hire an Unblinded Clinical Research Associate I with a permanent and full-time contract.

Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.

At Labcorp Drug Development, you will have autonomy to organize your work and in return, you will be supported and empowered to go beyond the typical CRA role, to really be an expert on your protocols and to own your sites.

Responsibilities include but are not limited to:
Responsible for all aspects of unblinded study site monitoring including routine visits and closing down sites

Monitoring pharmacy sites to ensure GCP compliance across studies

IMP management / accountability

Ensuring the pharmacy staff are properly trained

Checking prescriptions & chain of custody

Involvement in audits

Requirements:

If you are someone who is eager to constantly develop and improve while working in a friendly and collaborative team environment; then we are looking forward to meeting you.

Minimum 1 year of clinical monitoring experience in international Pharma/CRO company needed

CRA Certification

Experience in interventional studies preferred

Excellent understanding of Serious Adverse Event (SAE) reporting

Fluent in English

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.