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a Career with emd serono is an ongoing journey of Discovery: our 52,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, life science and performance materials. for 350 years and across the .....
responsibilities essential function:conduct and facilitate specific start-up activities such as feasibility, site identification, pre- Qualification, site regulatory package (srp) review and approval, Informed Consent (icf) customization, irb/iec .....
descriptionfor an exciting opportunity, tfs is currently looking for our next colleague to our global Project Management team! as a global Project Manager, you will have a vital role in managing our global projects and multidisciplinary study teams .....
responsibilities this role is fully dedicated to one large Pharmaceutical client. role is home based but will require work from client’s office in stockholm 1- 2 days per week.the Clinical site manager (csm) is the Clinical sites’ direct point .....
descriptionthe senior manager, Clinical operations leads the cross-functional study team in managing one or more global Clinical trials in oncology, ensuring that study milestones and deliverables are achieved according to the agreed quality .....
novimmune sa is a Drug Discovery and development company located in plan-les-ouates and basel, switzerland, that focuses on developing therapeutic Monoclonal Antibodies for inflammatory diseases and immune-related disorders. the pipeline is a .....
the lead Clinical Trial operations manager (lead ctom) is responsible for all operational aspects of Clinical Trial oversight including the delivery of every study on time within budget and scope in Compliance with gcp’s, sops and standards.the .....
responsibilities essential function:conduct and facilitate specific start-up activities such as feasibility, site identification, pre- Qualification, site regulatory package (srp) review and approval, Informed Consent (icf) customization, irb/iec .....
descriptionthe senior manager, Clinical operations is responsible for the management of clinical studies in multiple phases including, but not limited to, the development of study start-up materials, clinical supplies, case report forms, contracts .....
responsibilities * conduct country specific feasibility and/or site pre-Qualification* review and validate site identification list* collect and negotiate confidentially agreements (cda) as required* organize translations per .....
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