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Clinical Data Management Jobs in Berkshire

1 - 15 of 124
1 - 15 of 124
Search results - Clinical Data Management Jobs in Berkshire
Boehringer Ingelheim-Bracknell
Data Analytics Operations Manager - Product Development Quality Risk Management 12 month Contact As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product...
Boehringer Ingelheim-Bracknell
Data Analytics Operations Manager - Product Development Quality Risk Management As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle...
Boehringer Ingelheim-Bracknell
Data Analytics Operations Manager - Product Development Quality Risk Management 12 month Contact As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product...
mindmatch.ai -
Boehringer Ingelheim-Bracknell
Data Analytics Operations Manager - Product Development Quality Risk Management As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle...
Maidenhead
and other Safety MDs for assigned investigational programs including clinical trial activities (protocol review, ICF review, etc.), safety committee management, data analysis, signal detection, ad hoc requests and other product activities...
cv-library.co.uk -
Boehringer Ingelheim-Bracknell
Data Analytics Operations Manager - Product Development Quality Risk Management As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle...
Slough
on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.  •  Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.  •  Act as a central contact for the clinical team...
pharmiweb.jobs -
2 similar jobs: Reading, Newbury
Pro4orm People Ltd-Slough
Job Description Pro4orm People Ltd have partnered with a global pharmaceutical company in the search of a Senior Regulatory Affairs Manager. We are looking to speak to people who have an excellent understanding and experience of European...
SRG-Slough
attributes)  •  B.S., M.S. in health science  •  Advanced degree preferred (PharmD, or Ph.D., or equivalents)  •  Senior Manager RMPL - Minimum 5 years of broad and progressive pharma experience in medical, clinical or pharmacovigilance but with a clear focus...
Sanofi EU-Reading
professionals to communicate scientific data and gather insights  •  Contribute to medical strategy development, including launch planning and life-cycle management  •  Collaborate cross-functionally with clinical, regulatory, and commercial teams to ensure...
Reading
Our Client is an independently owned and operated company that works exclusively with clinical trial materials. The UK site provides secondary packaging, labelling and distribution of clinical trial supplies for sponsor company organisations...
cv-library.co.uk -
Planet Pharma-Maidenhead
for safety data. Additionally, the Senior PV Scientist supports Clinical Trial PV medical activities and serves as a Subject Matter Expert on global safety regulations, data analysis, and product-specific information for cross-functional teams. Objectives...
Reading
professional and ethical standards and clinical requirements To be responsible for leading, managing and delivering the specialist pharmacy service of oncology To provide advice and support to consultants, other clinicians and patients ensuring the safe...
cv-library.co.uk -
Pro4orm People Ltd-Slough
Pro4orm People Ltd have partnered with a global pharmaceutical company in the search of a Senior Regulatory Affairs Manager. We are looking to speak to people who have an excellent understanding and experience of European Regulatory requirements...
mindmatch.ai -
Planet Pharma-Maidenhead
for safety data. Additionally, the Senior PV Scientist supports Clinical Trial PV medical activities and serves as a Subject Matter Expert on global safety regulations, data analysis, and product-specific information for cross-functional teams. Objectives...
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