gcp qa sme - Basel, Basel
vor 1 Monat

Job summary
We are seeking a highly experiencedGCP QA Subject Matter Expert to support a leading Biopharma client during a period of rapid clinical portfolio expansion and integration activities.
This is a high-impact, hands-on role requiring a technical expert to ensure the highest standards of compliance participant safety and data integrity.
Stellenbeschreibung
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Zugang zu allen hochrangigen Positionen und den Job Ihrer Träume erhalten.
Ähnliche Jobs
gcp qa sme
vor 1 Monat
We are seeking a highly experienced GCP QA Subject Matter Expert to support a leading Biopharma client during a period of rapid clinical portfolio expansion and integration activities. · ...
Data Integrity Expert
vor 2 Wochen
+Permanent Consultant – Data Integrity Expert+ · Location: Basel Region, Switzerland+Data integrity compliance across GxP environments in line with Swissmedic, EU GMP and global regulatory requirements · +Role Overview For our consulting team in the Basel region we are seeking an ...
Data Integrity Expert
vor 2 Wochen
We are seeking an experienced Data Integrity Expert to support pharmaceutical and biotechnology clients in the Basel region. · Degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Engineering, or related field. · 5+ years of experience in Data Integrity, Quality Assurance ...
Clinical Associate Regulatory Submissions
vor 1 Monat
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. · ...
Clinical Associate Regulatory Submissions
vor 1 Monat
Clinical Associate Submissions – Regulatory: Homebased Austria Switzerland. IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. · ...
Senior Principal Statistical Programmer
vor 2 Wochen
+We are seeking key talent like you to join us and help give people with disease and their families a brighter future to look forward to. · +Lead statistical programming activities as Trial Programmer for several studies or as Lead/ Program Programmer for a medium to large sized ...
Senior Principal Statistical Programmer
vor 2 Wochen
We are seeking key talent to join our Development Team as a Senior Principal Statistical Programmer. As a key collaborator and strategic partner with biostatistics in ensuring that pharmaceutical drug-development plans are executed efficiently with timely and high-quality deliver ...
Senior Principal Statistical Programmer
vor 2 Wochen
The Senior Principal Programmer is responsible for all statistical programming aspects of several studies, a medium to large sized project or project-level activities (incl. submission and post-marketing activities) The position is a key collaborator and strategic partner with bi ...
Clinical Associate Regulatory Submissions
vor 1 Monat
Clinical Associate Submissions – Regulatory: Homebased in Austria, Switzerland. IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. · ...