Lifelancer
Your responsibilities include, but are not limited to: Responsibility for ensuring high quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team (iCTT) Perform high quality clinical data review and identify clinical data insights through…
10+ years\' experience in regulatory medical writing. Experience in authoring protocols, clinical study reports, investigators brochures, informed consent forms, summary documents, etc. Experience in multiple therapeutic areas, including but not limited to vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders,…
10+ years\' experience in regulatory medical writing. Experience in authoring protocols, clinical study reports, investigators brochures, informed consent forms, summary documents, etc. Experience in multiple therapeutic areas, including but not limited to vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders,…
Planning and working with the clinical programming group to schedule specification, programming, validation and ongoing delivery activities. Ability to write and execute SAS programs to produce internal and Sponsor deliverables. Leads timelines for programming setup process, ensuring issues are addressed…
Role We have a few Pharma & Life Sciences Consultant roles for our clients at Lifelancer. Create your profile on the Lifelancer platform & apply soon to grab the opportunity. Other roles There are several remote & freelance jobs in…