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Must Have Skills (Top 3 technical skills only)*:

Monitoring clinical trials in Sitesfield Clinical drug development Experience in human genetics, gene mutations, investigational therapeutic agents and biologics

Detailed Job Description:

Clinical drug development monitoring clinical trials in Sitesfield Early product development, study design protocolinformed consentstudy reports, narratives, scientific papers in peer review journals, CRO selectionmanagement, phase IIV trials Experience in human genetics, gene mutations, investigational therapeutic agents and biologics

Certifications Needed: No

Responsibilities you would expect the Subcon to shoulder and execute*:

Early product development, study design protocolinformed consentstudy reports, narratives, scientific papers in peer review journals, CRO selectionmanagement, phase IIV trials

Interview Process (Is face to face required?) No