Parexel - Serbia

Lead global clinical trial site activation for a pharmaceutical sponsor. Utilize your 4-6 years of regulatory submission and project management experience in Pharma/CRO. Based in Serbia, you will develop strategies, oversee CRO performance, and ensure efficient, compliant study start-up.

Join Parexel as a Senior Statistical Programmer, fully home-based in Serbia. Utilize your 5+ years of SAS programming and CDISC expertise to analyze clinical trial data and support submissions. Enjoy a flexible role with extensive training, a supportive environment, and long-term career growth in...