Remote Oncology Clinical Scientist (Contract)

AL Solutions; États-Unis; À distance; USD 120 000 - 180 000; Plein temps

Résumé du poste

AL Solutions is seeking an experienced Clinical Scientist for a fully remote contract role supporting oncology clinical development programs. You will design, oversee, and contribute to the execution of oncology studies, collaborating with cross-functional teams to ensure robust scientific integrity and timely study delivery.

Ideal candidates will have 7+ years in a Clinical Scientist role, demonstrated ability to lead global teams, and extensive experience in high-volume oncology trials.

Qualifications

• 7+ years of experience as a Clinical Scientist.
• Experience leading a global team.
• Experience with high volume studies in pharma/biotech/CRO settings.
• Strong background in oncology clinical development programs.
• Understanding of clinical trial design, conduct and data analysis.
• Experience contributing to CSRs and other development documentation.
• Excellent communication and stakeholder management, able to work remotely.

Responsabilités

• Provide scientific oversight for oncology clinical studies.
• Contribute to protocol development, study design, clinical documents and execution activities.
• Assist with data review, interpretation and clinical study reporting.
• Collaborate with Clinical Operations, Biostatistics, Medical Writing, Regulatory Affairs and external stakeholders.
• Support safety review activities and participate in study team meetings.
• Review clinical data trends and ensure scientific integrity across the study lifecycle.
• Engage in investigator interactions, medical monitoring support and study-related scientific discussions.

Connaissances

Clinical trial design

Data analysis

Regulatory knowledge

Stakeholder management

Remote collaboration

Oncology clinical development

Study protocol development

Description du poste

AL Solutions is seeking an experienced Clinical Scientist for a fully remote contract role supporting oncology clinical development programs. You will design, oversee, and contribute to the execution of oncology studies, collaborating with cross-functional teams to ensure robust scientific integrity and timely study delivery.

Ideal candidates will have 7+ years in a Clinical Scientist role, demonstrated ability to lead global teams, and extensive experience in high-volume oncology trials.