Our client is a global pharmaceutical company and is at the forefront of developing and marketing life changing products that prevent and treat illness.
they want people with the drive to make a difference to health and general well being. Monitoring clinical studies in phases II-III Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
Identification, qualification and initiation of investigators and their sites. CRA II Home Based Berlin Permanent / Berlin Germany Supervising study conduct according to GCP requirements and all applicable laws.
from € 48,000 p.a. Our client is one of the world's largest CRO, supporting Pharmaceutical & Biotech companies... More details.
a. Experience with site initiation, site close out Our client is one of the world's largest CRO, supporting Pharmaceutical & Biotech companies.
0 Clinical Programmer Czech Republic Permanent / Prague Czech Republic up to