Clinical Scientist

AL Solutions; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

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.

Responsibilities

• 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.

Skills

Clinical trial design

Data analysis

Regulatory knowledge

Stakeholder management

Remote collaboration

Oncology clinical development

Study protocol development

Job description

We are partnering with a growing US-based CRO to appoint an experienced Clinical Scientist on contract basis who will be outsourced to a sponsor. This is a fully remote opportunity supporting oncology clinical development programs, offering the chance to work closely with cross-functional teams on the design, execution, and oversight of clinical trials.

This position is ideal for a Clinical Scientist with strong oncology experience who thrives in a fast-paced, collaborative environment and can quickly contribute to ongoing studies.

Key Responsibilities

• Provide scientific oversight and support for clinical studies within oncology indications.
• Contribute to protocol development, study design, clinical documents, and study 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 help ensure scientific integrity throughout the study lifecycle.
• Contribute to investigator interactions, medical monitoring support, and study-related scientific discussions.

Required Experience

• 7+ years experience working as a Clinical Scientist within the pharmaceutical, biotech, or CRO environment.
• Experience in leading a global team.
• Experience with high volume studies.
• Strong experience supporting oncology clinical development programs.
• Understanding of clinical trial design, conduct, and data analysis.
• Experience contributing to study protocols, CSRs, and other clinical development documentation.
• Strong communication and stakeholder management skills.
• Ability to work independently in a remote environment and hit the ground running.

Preferred Experience

• Experience supporting Phase II and/or Phase III clinical trials.
• Previous CRO experience.
• Knowledge of regulatory requirements and GCP guidelines.
• Exposure to multiple oncology indications.