As a leading contract research organization (CRO), Labcorp Drug Development (formerly known as Covance) 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 FSPx business in Hungary and are currently seeking to hire an Unblinded CRA I and Unblinded CRA II with a permanent and full-time contract. In this role, you will be sponsor-dedicated. Depending on your experience level and location, the position can be be home-based or office-based.

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 be yond the typical CRA role, to really be an expert on your protocols and to own your sites.

Responsibilities include but are not limited to:

• Ensuring accurate pharmacy documentation is in place
• Ensuring investigational medicinal product (IMP) accountability is maintained and blinded and unblinded site staff members can work in a coordinated manner without compromising the blind
• Maintaining IMP supplies in suitable storage conditions and ensuring they are accurately reconstituted, dispensed, administered, returned and destroyed
• Maintaining all appropriate documentation and ensuring a study drug re-supply procedure will be put in place where necessary

Education/Qualifications:
Life Science degree (preferred) or similar qualification
Experience:

• Previous experience in clinical monitoring is preferred but it is not a firm requirement for UCRA I position
• Previous experience in clinical monitoring is required for UCRA II position
• Excellent understanding of Serious Adverse Event (SAE) reporting
• Ability to resolve project-related problems and prioritize workload for self and team
• Fluency in Hungary and solid English skills