Clinical Scientist

Kelly Science, Engineering, Technology & Telecom; United States; On-site; 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 is seeking a Clinical Scientist for a long-term remote engagement supporting a global pharmaceutical client. This individual will work closely with the Clinical Scientist Protocol Lead and study team to support the clinical and scientific execution of clinical studies.

Key Responsibilities

• Assist the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studies
• Support medical monitoring activities, adjudication, imaging data reconciliation, and preparation of study meeting materials
• Review clinical study data and assist with identification and resolution of data discrepancies and queries
• Support protocol deviation review and management
• Review patient data, including adverse events, laboratory results, endpoints, and other clinical information
• Support one or multiple clinical studies depending on study needs
• May lead a study or workstream with limited scope, such as survival follow-up
• Interact with internal and external stakeholders, including study sites and committees, to support clinical study objectives

Qualifications

• Degree in Life Sciences required (BS/BA/MS/PhD)
• Minimum of 2 years of pharmaceutical and/or clinical drug development experience within the last 5 years
• Experience may come from pharmaceutical/biopharmaceutical companies, CROs, hospitals, research sites, clinical trial units, or SMOs
• Experience reviewing and resolving study-related data issues, including queries and medical record/data review
• Ability to identify data discrepancies requiring clarification with clinical study sites
• Experience reviewing patient data and resolving discrepancies involving adverse events, laboratory results, endpoints, and safety data preferred
• Therapeutic-area experience required for Oncology positions; indication-specific experience preferred
• Strong written and verbal communication skills
• Proficiency with Microsoft Outlook, Word, Excel, and PowerPoint; OneNote experience preferred