Clinical Associate Regulatory Submissions - Basel, BS
vor 1 Monat
Jobbeschreibung
, 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
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. · ...
vor 1 Monat
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. · ...
vor 1 Monat
We are looking for a Consultant Labelling & Compliance to join our teams in Zug to support global labelling regulatory compliance and quality activities for in vitro diagnostic IVD products across their full lifecycle. · Manage and coordinate IVD product labelling activities in a ...
vor 1 Monat
Sobi is a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. · ...
vor 3 Wochen
The Global Regulatory CMC Lead develops and executes global regulatory CMC strategy for assigned Sobi assets in development prepares CMC sections of IND/IMPD MAA NDA/BLA as well as assesses global filing strategy for post approval changes. · ...
vor 1 Woche
Executive Director, HTA Strategy, Europe
Nur für registrierte Mitglieder
The Executive Director will lead the end-to-end execution of EU Joint Clinical Assessments and Joint Scientific Consultations across Revolution Medicines' oncology portfolio. · ...
vor 2 Wochen
We are seeking passionate individuals to join our innovative team at Novartis. · You will work with cutting-edge technology and collaborate with experts in patient safety · Provide expert safety input to the clinical development program for assigned projects/products. · Manage sa ...
vor 4 Wochen
We are seeking passionate individuals to join our innovative team. You will work with cutting-edge technology, collaborate with experts and drive excellence in patient safety. · ...
vor 4 Wochen
The Global Head of PD Regulatory · is a visionary executive responsible for steering a bold, distinctive, and data-first organization. · This role demands an individual who can make rapid strategic decisions as the global landscape evolves, · ensuring that the company's drug and ...
vor 1 Tag
An exciting opportunity exists for experienced Patient Safety Physicians to contribute to the oversight of drug safety across multiple therapeutic areas. · Designing and implementing strategies to generate robust safety evidence · Developing patient-centric risk minimization and ...
vor 4 Wochen
BioVersys is a Swiss clinical-stage biotech company dedicated to the development of innovative antibacterial therapies addressing the global crisis of antimicrobial resistance. The company offers a unique opportunity to contribute to life-saving innovation in infectious diseases ...
vor 2 Wochen
We are seeking a Technical Regulatory Affairs CMC Associate Director to strengthen the team in 2026 in support of Phase 3 development activities. · ...
vor 3 Wochen
BioVersys is a Swiss clinical-stage biotech company dedicated to developing innovative antibacterial therapies addressing antimicrobial resistance. The Senior CMC Project Manager will drive CMC development activities across BioVersys' small molecule pipeline. · ...
vor 2 Tagen
We are seeking an Executive Director to lead our Health Technology Assessment (HTA) strategy in Europe. · ...
vor 2 Wochen
Vice President, Regulatory Affairs, Europe and International
Nur für registrierte Mitglieder
The Vice President, Europe and International Regulatory Affairs (APAC and New Markets, excluding USA, China and Japan), is a leadership position that will be responsible for building and leading the regulatory groups to develop and implement regulatory strategies to secure and ma ...
vor 3 Wochen
We are looking to appoint an experienced Regulatory Manager to join our close-knit technical team. · You will lead and coordinate substance dossier preparation for EU and Swiss submissions, · provide hands-on technical input into risk assessments · and study report summaries, · c ...
vor 13 Stunden
Shape the Future of Patient-Centered Medical Device Innovation For our client, a globally leading pharmaceutical company driving innovation in life sciences and patient care, we are seeking a dedicated Human Factors Engineer to support critical regulatory submissions for parenter ...
vor 1 Monat
JOB DESCRIPTION At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both persona ...
vor 6 Stunden
Vice President, Regulatory Affairs, Europe and International
Nur für registrierte Mitglieder
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. · ...
vor 3 Tagen
The Senior Regulatory Affairs Manager manages assigned regulatory and cross-functional projects; provides strategic and operational support to Veristat clients in regulatory decision-making processes. · ...
vor 1 Woche