EU CTR Submission Lead - Warszawa

We are looking for a Regulatory Affairs Manager to join our small team and lead several Regulatory Affairs activities for an established and developing generics portfolio. · This role will have a main focus on European submissions through MRP, DCP, and National procedures. · ...

· We are recruiting for a Regulatory Affairs Senior Specialist – Publishing to join a growing Regulatory Publishing team at an international Contract Research Organization. · ​ · Our client is an established CRO with years of experience and expertise in clinical research. Their ...

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. · Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. · Required degrees, c ...

This role offers opportunities to work with colleagues across regions, develop your skills, and contribute to high-impact projects that strengthen the firm's resiliency. · ...

+The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. · ...

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. · ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production lin ...

We are seeking a Regulatory Affairs Manager with proven Global Regulatory Lead experience to drive global regulatory strategies and submissions for human medicinal products. You will own the regulatory roadmap, and coordinate worldwide filings across major agencies including EMA ...

Due to ongoing global expansion Indero is looking to hire a Regulatory Affairs Specialist responsible for preparation and submission of part I and/or part II following EU CTR and other applications created within or outside of the company. · ...

We are looking to bring medicines to the world faster without compromising on excellence and integrity. As a Senior Manager Submissions Strategy you will be responsible for directing the development quality control and publication of submissions relating to asset development regi ...

Bristol Myers Squibb es una empresa innovadora donde puedes trabajar en proyectos transformadores que cambian vidas. · Collabora con stakeholders clave para definir estrategias e IND y marketing submission. · Revisa entregables principales para asegurar cumplimiento. · ...

We are seeking a Regulatory Affairs Manager with proven Global Regulatory Lead experience to drive global regulatory strategies and submissions for human medicinal products. · Bachelor's or Master's degree in Life Sciences or related fieldEight or more years in Regulatory Affairs ...

Senior Regulatory ScientistICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical develo ...

Description · Junior Publication Project Coordinator · About Astellas · Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, ...

Bristol Myers Squibb es una empresa que ofrece oportunidades laborales innovadoras y significativas para transformar vidas. · ...

Challenging meaningful life-changing those aren't words that are usually associated with a job but working at Bristol Myers Squibb is anything but usual here uniquely interesting work happens every day in every department from optimizing a production line to the latest breakthrou ...

Freyr is a fast-growing company specializing in regulatory solutions for the Life Sciences industry. · ...

Join JP Morgan Chase & Co., a global leader in financial services to lead innovative projects enhancing data governance and regulatory reporting. · ...

We are seeking a Regulatory Affairs Manager with proven Global Regulatory Lead experience to drive global regulatory strategies and submissions for human medicinal products. · This role will own the regulatory roadmap, and coordinate worldwide filings across major agencies includ ...

Site Name: Belgium-Wavre, Bangalore, GSK HQ, Siena, Stevenage, Warsaw · Posted Date: Feb · Business Introduction · At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering a ...

Description · Join a collaborative team where you will help drive innovation in regulatory planning and develop your expertise in capital and liquidity management. This role offers opportunities to work with colleagues across regions, enhance your technical skills, and contribute ...