Clinical Scientist

Description Of Services

• 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
• Supports a single study or multiple studies
• May lead a study with limited scope (e.g., Survival Follow-up)
• Interacts with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Minimum Years Of Experience

• 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, required
• TA-specific experience required for postings in Oncology
• TA-specific experience in IDV and GSM preferred
• Indication specific experience preferred
• 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, etc., required

Skills

• Proficient in reviewing patient data and resolving discrepancies in the following areas: adverse events, trends of adverse events, end point management, labs experience, preferred
• Demonstrated oral and written communication skills
• Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required. One Note experience preferred.

Education

• 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.

As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account.

In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.