Manager Clinical Affairs Jobs in Hessen
1 - 15 von 16
Suchergebnisse - Manager Clinical Affairs Jobs in Hessen
ARCONDIS AG / GmbH-Frankfurt
Manufacturing Practices (GMP), Quality System Regulations (QSR), and Good Clinical Practices (GCP).
• Willingness to travel.
• Professional certification in Regulatory Affairs (RAC) is preferred.
• Experience with Class II and Class III medical devices and ATMPs...
appcast.io -
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
LEO Pharma GmbH-Neu-Isenburg
similar role
• Minimum of 10 years demonstrable experience, within the pharmaceutical industry, in medical affairs and or in clinical research and development
• Solid knowledge of drug development, safety, regulatory, market access and reimbursement...
stepstone.de -
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
Mundipharma International-Frankfurt
as well as life cycle management. The role plays a key part in the country leadership team for Germany and is expected to be a key contributor to the Cluster Leadership team and Global Market Access network. This position will have a highly matrixed...
appcast.io -
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
CSL Behring-Hattersheim am Main
compliant. Provides advice to management and updates controlled documents and platforms to align with evolving regulations.
• Establishes good working relationships with GSPV, Global Regulatory Affairs (GRA) and local functions, such as Local Quality Officer...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
CSL Behring-Frankfurt am Main
compliant. Provides advice to management and updates controlled documents and platforms to align with evolving regulations.
• Establishes good working relationships with GSPV, Global Regulatory Affairs (GRA) and local functions, such as Local Quality Officer...
6 ähnliche Jobs: Offenbach, Kassel, Frankfurt, Darmstadt, Wiesbaden...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
STADA Arzneimittel AG-Bad Vilbel
years of experience in Regulatory affairs incl. global positions You have a proven track record of achieving drug approvals from different health authorities, in particular FDA, EMA, Swissmedic, additional experience with e.g. COFEPRIS, ANVISA, PMDA...
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