Clinical Scientist

Kelly Science & Clinical FSP provides scientific and clinical staffing support for pharmaceutical clients. The Clinical Scientist will support the clinical and scientific execution of clinical studies by assisting with medical monitoring, reviewing patient and study data, managing protocol deviations, and coordinating with study stakeholders.

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

Preferred

Experience reviewing patient data and resolving discrepancies involving adverse events, laboratory results, endpoints, and safety data preferred

Patient Data Review

Discrepancy Resolution

Adverse Events Analysis

Laboratory Results Evaluation

Safety Data Management

Benefits

Long-term remote engagement

Company

Technical staffing and SOW services for science, engineering, technology

Troy, Michigan, USA

https://set.kellyservices.us/

Founded in 1946

5001-10000 employees

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

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

Experience reviewing patient data and resolving discrepancies involving adverse events, laboratory results, endpoints, and safety data preferred

Required skills

Pharmaceutical Drug Development, Clinical Drug Development, Clinical Study Data Review, Medical Record Review, Data Query Resolution, Data Discrepancy Identification, Patient Data Review, Adverse Event Review, Laboratory Results Review, Endpoint Review, Safety Data Review, Microsoft Office Outlook, Microsoft Office Word, Microsoft Office Excel, Microsoft Office PowerPoint

Experience

2+ years