Remote Clinical Scientist - Oncology Studies

Kelly Science, Engineering, Technology & Telecom; United States; Remote; USD 90,000 - 150,000; Full time

Job summary

Kelly Science & Clinical FSP seeks a Clinical Scientist for a long-term remote engagement supporting a global pharmaceutical client. The role collaborates with the Clinical Scientist Protocol Lead and study team to advance clinical and scientific execution of studies.

Responsibilities include assisting with clinical/scientific conduct, medical monitoring, data reconciliation, adverse events review, and coordinating with sites and committees.

Qualifications

• Degree in Life Sciences (BS/BA/MS/PhD) required.
• 2+ years in pharma/clinical drug development in last 5 years.
• Experience reviewing data issues and medical records.
• Ability to identify data discrepancies with study sites.
• Oncology therapeutic-area experience preferred.
• Strong written and verbal communication skills.

Responsibilities

• Assist Protocol Lead with the clinical/scientific conduct of studies.
• Support medical monitoring, adjudication, imaging reconciliation, and materials.
• Review study data and resolve data discrepancies.
• Support protocol deviation review and management.
• Review patient data including adverse events, labs, endpoints, and safety.
• Support one or multiple studies as needed.
• May lead a study or workstream with limited scope.
• Interact with sites and committees to meet objectives.

Skills

Communication skills

Data review and discrepancy resolution

Clinical study support

Team coordination

Education

Life Sciences degree (BS/BA/MS/PhD)

Tools

Microsoft Outlook

Microsoft Word

Microsoft Excel

PowerPoint

OneNote

Job description

Kelly Science & Clinical FSP seeks a Clinical Scientist for a long-term remote engagement supporting a global pharmaceutical client. The role collaborates with the Clinical Scientist Protocol Lead and study team to advance clinical and scientific execution of studies.

Responsibilities include assisting with clinical/scientific conduct, medical monitoring, data reconciliation, adverse events review, and coordinating with sites and committees.