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Senior Quality Specialist
UNITED KINGDOM, , UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Position overview The Senior Quality Specialist...
Director, Drug Safety Lead
CAMBRIDGE
...clinical safety and pharmacovigilance support to medicines across life cycle. Reporting to the Head of Drug Safety, this key role will lead the clinical safety activities for the assigned compounds within the organization. br br /p p You will be accountable for the implementation...
Engagement Manager - R&D (Remote)
LONDON, ENGLAND, UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You'll Do Lead multiple project engagement teams empowering the team to plan and manage all aspects of delivery, from scope to quality assurance Be responsible for the end-to-end design, build, and delivery of...
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Senior Quality Specialist
UNITED KINGDOM, UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. /p p br /p p b Position overview /b...
Head of Regulatory Affairs
46547
EAST KILBRIDE, SOUTH LANARKSHIRE
...manufacturing, quality assurance, (pharmacovigilance), marketing and commercial Interfacing with Competent Authorities globally Ability to travel as requiredQualifications: Either Degree in Life Science or track record in a similar position Member of TOPRA is desirable Regulatory experience in...
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Director, Drug Safety Lead
CAMBRIDGE, ENGLAND, UNITED KINGDOM
...clinical safety and pharmacovigilance support to medicines across life cycle. Reporting to the Head of Drug Safety, this key role will lead the clinical safety activities for the assigned compounds within the organization. You will be accountable for the implementation, execution, and...
Computer System Compliance Auditor
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice...
Multilingual Medical Information Specialist - Norwegian Speaking
UNITED KINGDOM, , UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. The Multilingual Medical Information Specialist...
Technical Support Analyst
UNITED KINGDOM, , UNITED KINGDOM
...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. Our mission Our mission is to provide industry-defining implementations that are fast and intuitive to bring our customers an enjoyable and efficient experience. Widely regarded by our customers...
Key Account & Access Manager - Diabetes
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
...reporting in this area. Pharmacovigilance-Reporting: The Biocon employee should follow and apply within 24h the standard Biocon PV approach if becoming aware about adverse events/side effects and/or incidents including lack of efficacy for Biocon products. Pharmacovigilance department by any of...
Support and Development Liaison
UNITED KINGDOM, , UNITED KINGDOM
...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. Our mission Our mission is to provide industry-defining implementations that are fast and intuitive to bring our customers an enjoyable and efficient experience. Widely regarded by our customers...
Multilingual Medical Information Specialist - Norwegian Speaking
...amp; compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. /p p br br The experience expected...
Senior Quality Specialist
...amp; compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. /p p br /p p strong Position...
Computer System Compliance Auditor
ENGLAND, ENGLAND
p ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory...
Computer System Compliance Auditor
£60 - 80
LONDON
...Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (together, GxP). br br Founded in 2007, ADAMAS has focused on ensuring that the highest standards of best practice are attained across...
Technical Support Analyst
UNITED KINGDOM, UNITED KINGDOM
...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. /p p br /p p b Our mission /b /p p Our mission is to provide industry-defining /p p implementations that are fast and intuitive to bring our customers an enjoyable and efficient...
Technical Support Analyst
...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. /p p br /p p strong Our mission /strong /p p Our mission is to provide industry-defining /p p implementations that are fast and intuitive to bring our customers an enjoyable and...
Engagement Manager - R&D (Remote)
£100 - 125
LONDON, REMOTE
...Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. /p b What You'll Do /b ul li Lead multiple project engagement teams – empowering the team to plan and manage all aspects of delivery, from scope to quality assurance /li li Be responsible for the end-to-end...
Key Account & Access Manager - Diabetes
BIRMINGHAM
...li /ul p br /p p Pharmacovigilance-Reporting: /p ul li The Biocon employee should follow and apply within 24h the standard Biocon PV approach if becoming aware about adverse events/side effects and/or incidents including lack of efficacy for Biocon products. /li li Pharmacovigilance...
Support and Development Liaison
...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. /p p br /p p strong Our mission /strong /p p Our mission is to provide industry-defining /p p implementations that are fast and intuitive to bring our customers an enjoyable and...
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