Experienced Clinical Research Associate

Reference No: RO – ECRA

For our Bucharest office we are seeking to employ:

Experienced Clinical Research Associates with at least one year of experience in monitoring clinical trials.

Description summary:
The CRA will be responsible for performing and coordinating all aspects of clinical monitoring in compliance with ICH/GCP guidelines and the company SOPs. The CRA will conduct site visits to determine protocol and regulatory compliance.

Education and experience:

• Degree in a life science or related field
• Monitoring experience with a CRO, pharmaceutical or biotech company

Requirements:

• Excellent clinical trials monitoring skills
• In-depth understanding of ICH/GCP guidelines
• Mastered oral and written communication skills with the ability to communicate effectively with medical personnel
• Highly organized with strong attention to detail, deadlines and ability to multitask
• Excellent English
  
• Advanced skills across all of the Microsoft packages
• Willingness to travel
  

We offer extensive corporate trainings, attractive salary, full package of benefits and performance-based bonuses to the right candidates.

Please submit to jobs@abcro.com by using the Reference No as a subject:

• Your resume
• A cover letter describing why your experience and skills make you a good candidate for this position

AbCRO, Inc. is an equal opportunity employer.