TRABAJO REGULATORY AFFAIRS CLINICAL WRITING
(129 ofertas de trabajo)
Listado de trabajos de Regulatory affairs clinical writing
Regulatory affairs specialist latvia
Provide support and guidance to the baltic regulatory team on all regulatory matters in latvia... support regulatory inspections and audits and facilitate timely...
Clinical affairs program manager spain
They are looking for a clinical affairs program manager europe... as part of the global clinical affairs team, you will be responsible for developing strategies...
Responsibilities:manages a team of regulatory affairs employees... headcount, experience, training) to sustain regional activities of regulatory affairs group...
Translational regulatory affairs director
This requires early anticipation of the potential regulatory impact and developing capabilities to design regulatory strategies applicable to late development projects...
Regulatory affairs associate xiromed
Awareness or regulatory affairs environment, eu-wide legal framework, and european authorities’ websites... profilewe are looking for a dynamic, capable, curious...
Regulatory affairs manager - (swiss submissions, home-based) (m/w/d)
The manager, regulatory affairs international supports ambitious geographical expansion plans... establish and maintain contact with the national regulatory authorities...
Regulatory affairs specialist emea m/f (1 year contract)
We are zimvie, a publicly traded, global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients’ smiles, function...
Regulatory intelligence director oncology
The rid will work closely with therapeutic area (ta) vp, executive regulatory science directors, global regulatory leaders (grls) and regulatory affairs directors...
Senior regulatory science and strategy lead - emea real world solutions
The role interacts with regulatory and drug development leaders around iqvia relative to customers who require regulatory expertise... secondly, the role encompasses...
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Director clinical scientist - hematology early oncology r&d
clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...
Associate director, clinical project scientist (oncology)
The clinical scientist provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and clinical...
Senior field clinical specialist (m/f/d) electrophysiology
Facilitate communication between clinical sites and other abbott clinical staff (e... maintain and develop a productive clinical territory: develop and maintain...
Global medical affairs leader, director, dermatology
Excellent knowledge of study execution, benefit risk management and regulatory affairs... a demonstrated track record of success within medical affairs and/or clinical...
Global clinical development scientist director - vaccines and immune therapies
Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... understanding of scientific and clinical...
Pharma product manager - connected regulatory intelligence
The role will work on several regulatory software applications that leverage the connected regulatory intelligence platform... pharma product manager - connected...
Associate medical director, clinical development sciences
Engage with clinical investigators on clinical studies to enable quality clinical execution, analyze and interpret clinical data, and collaborate with the broader...
Medtech business analyst - connected regulatory intelligence
Medtech business analyst - connected regulatory intelligence the iqvia connected regulatory intelligence (cri) is a groundbreaking innovative solution that simplifies...
Pharma business analyst - connected regulatory intelligence
Pharma business analyst - connected regulatory intelligence the iqvia connected regulatory intelligence (cri) is a groundbreaking innovative solution that simplifies...
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