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Vita Global Sciences, a Kelly Company · 1 week ago

Clinical Scientist

United States

Contract

Remote

Entry, Mid Level

$60/hr - $60/hr

2+ years exp

Vita Global Sciences, a Kelly Company, is seeking a Clinical Scientist for a long-term remote engagement with a Global Pharmaceutical client. The role involves assisting with the clinical/scientific conduct of clinical studies, supporting study teams, and interacting with stakeholders to meet clinical study objectives.

AnalyticsData VisualizationInformation Technology

No H1B

Responsibilities

Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g, adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management

May support a single study or multiple studies

May lead a study with limited scope (e.g., Survival Follow-up)

May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Qualification

Clinical drug developmentData reviewOncology experienceMicrosoft OfficeLife Sciences degreeOral communicationWritten communication

Required

At least 2 years Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years

Experience reviewing and resolving study related data issues such as: issued queries, resolved queries, accurate review of medical records, identify any errors in data by performing data review that require further clarification with the study sites

Demonstrated oral and written communication skills

Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint)

Degree in Life Sciences

BS/BA/MS/PhD

Applicants must be currently authorized to work in the US on a full-time basis now and in the future

Preferred

TA-specific experience in IDV and GSM

Indication specific experience

Proficient in reviewing patient data and resolving discrepancies in the following areas: adverse events, trends of adverse events, end point management, labs experience

One Note experience