Medical Affairs Jobs in Berkshire
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Search results - Medical Affairs Jobs in Berkshire
Maidenhead
Medical Affairs Operations Associate
Job Type: Temporary
Location: Berkshire
Duration: 12 month contract
SRG are partnered with a leading Global Pharmaceutical Company who have an opportunity for a Medical Affairs Operations Associate...
cv-library.co.uk -
myGwork-Reading
authorities) and associations (incl PAGB and other competent associations), as well as internal stakeholders including Enterprise/Regional Regulatory Affairs, Local commercial, Medical, PV and Quality
• Evaluation, preparation, communication...
Parkside Recruitment-Windsor
and guidance documents, e.g., in the area of Computerised System Validation, Data Integrity, Manufacturing, Pharmacovigilance, Clinical Development, Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance
• Experience as a Lead Auditor...
mindmatch.ai -
Proclinical Staffing-Reading
candidate will work with pharmaceuticals, medical devices, and nutraceuticals regulatory frameworks, ensuring compliance and fostering a culture of continuous improvement.
Responsibilities:
• Develop and execute UK regulatory and quality strategies aligned...
Fortrea-Maidenhead
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical...
CSL Seqirus-Reading
products
• Lead collaboration with international markets to align pricing and access strategies with market changes.
• Work closely with HEOR and Medical Affairs to enhance the value proposition through updates to the Global Value Dossier and new cost...
mindmatch.ai -
Boehringer Ingelheim-England
as valuable education partners in improving patient care. Develop and foster high quality cross functional relationships with Boehringer-Ingelheim colleagues, both within Medical Affairs and especially outside this team, with local promotional teams to ensure...
jmmst.com -
CSL Seqirus-Newbury
products
• Lead collaboration with international markets to align pricing and access strategies with market changes.
• Work closely with HEOR and Medical Affairs to enhance the value proposition through updates to the Global Value Dossier and new cost...
mindmatch.ai -
Biogen-Maidenhead
leadership at all levels, ensuring strong collaboration between Sales, Marketing, Market Access, Medical, External Affairs, CE&O and other departments.
• Develop and execute comprehensive marketing plans that analyse markets and define short and long-term...
smartrecruiters.com -
CSL Seqirus-Maidenhead
with HEOR and Medical Affairs to enhance the value proposition through updates to the Global Value Dossier and new cost-effectiveness and budget impact models.
• Gather and analyze insights on access requirements and market dynamics, including updates...
joblookup.com -
Planet Pharma-England
extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency.
We...
jmmst.com -
CSL Seqirus-Slough
products
• Lead collaboration with international markets to align pricing and access strategies with market changes.
• Work closely with HEOR and Medical Affairs to enhance the value proposition through updates to the Global Value Dossier and new cost...
mindmatch.ai -
Planet Pharma-England
We have extensive functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business...
jmmst.com -
Hamlyn Williams-England
Development, and Regulatory Affairs, to support validation efforts.
• Investigate and resolve validation deviations, anomalies, and non-conformances.
• Author and review Standard Operating Procedures (SOPs), User Requirement Specifications (URS...
Hamlyn Williams-England
Development, and Regulatory Affairs, to support validation efforts.
• Investigate and resolve validation deviations, anomalies, and non-conformances.
• Author and review Standard Operating Procedures (SOPs), User Requirement Specifications (URS...
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