Senior Clinical Scientist, Clinical Development
Drive development of protocols/protocol amendments for clinical studies. Prepare and/or provide input to clinical study related and other regulatory documents (e.g. CSRs, IBs, PIS/ICFs, SAPs, Data Management Plans, Safety Management Plan, Medical Monitoring Plan, SRC Charter, IND, briefing books)
Associate Medical Director Oncology, Clinical Development
Be an integral member of the clinical development team and the clinical study team and drive execution of the clinical study in partnership with other functions
Senior Global Clinical Trial Manager Phase 3
Develop clinical strategy for the therapeutic area in the assigned oncology program(s) (oncology – hematology) taking into account current medical practice and unmet needs; advances in both biological sciences and data sources; as well as competitive environment
Senior/Principal Biostatistician, Global Clinical Development
Provide expert statistical input to the design, analysis and interpretation of clinical studies, and development plans, primarily within Oncology
Senior Global Clinical Trial Manager Phase I & II
Develop clinical strategy for the therapeutic area in the assigned oncology program(s) (oncology – hematology) taking into account current medical practice and unmet needs; advances in both biological sciences and data sources; as well as competitive environment
Develop clinical strategy for the therapeutic area in the assigned oncology program(s) (oncology – hematology) taking into account current medical practice and unmet needs; advances in both biological sciences and data sources; as well as competitive environment
Senior Medical Director, Endocrinology & Rare Disease
Develop clinical strategy for the therapeutic area in the assigned oncology program(s) (oncology – hematology) taking into account current medical practice and unmet needs; advances in both biological sciences and data sources; as well as competitive environment
Executive Medical Director Oncology Clinical Development
Develop clinical strategy for the therapeutic area in the assigned oncology program(s) (oncology – hematology) taking into account current medical practice and unmet needs; advances in both biological sciences and data sources; as well as competitive environment
Scientist, Clinical Pharmacology and Pharmacometrics
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
Associate Principal Scientist Clinical Pharmacology
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
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