Biostatistics Consultant – Remote (Part-time, 10-15hrs/week)
Orbis Clinical is seeking a remote-based Biostatistics Consultant for 6 months.Job Title: Biostatistics ConsultantLocation: RemoteContract: 6 monthsSchedule: Initially working 10-15 hours a week for the first three months, then scaling back to 5-10 hours per week until the engagement endsBiostatistics ConsultantThe
Temp – Biostatistician (Gen Med & Internal Med) – REMOTE
Orbis Clinical is seeking a remote based Temp - Biostatistician ( (multiple openings) ) for a 6 month contract.Job Title: Temp - Biostatistician (General Med) - REMOTELocation: Remote (EST hours preferred)Contract: 6 monthsMost ideal candidate background: Sponsor-side or sponsor-embedded PhD/MS biostatistician with
Principal Medical Affairs Biostatistician (US)- REMOTE
Orbis Clinical is seeking a remote-based Principal Medical Affairs Biostatistician for 6 months.Brief Description:The Principal Biostatistician will be responsible for performing, and validating statistical analyses in support of Medical Affairs, inclusive of overseeing the work of statistics and programming for
Senior Principal Biostatistician (US)-REMOTE
Orbis Clinical is seeking a remote-based Senior Principal Biostatistician for 6 months.The Principal Biostatistician will be responsible for performing and validating statistical analyses in support of the clinical trial portfolio, in accordance with departmental SOP and guidelines, as needed and
Biostatistician III
Orbis Clinical is seeking a remote-based Biostatistician for 12+ months.Job Description : The Statistical Sciences Contractor will support the execution of the PULSEcheck (Progressive Uptake of Live Scientific Evaluation) initiative by partnering with study teams to monitor ongoing clinical trials
Director, Biostatistics – REMOTE
Orbis Clinical is seeking a remote-based Director, Biostatistics for 12 monthy.The Director, Biostatistics will be a leader of biostatistics and will oversee and provide statistical support to the development of client's therapeutics in close collaboration with Clinical Development, Regulatory Affairs,
