Clinical Scientist (Boston, MA; Dallas, TX; ...)

• Contribute to clinical study protocols, informed consent forms, and related documents.
• Analyze scientific data and literature to support clinical strategies.
• Collaborate with cross-functional teams to align study designs with objectives and regulations.
• Provide scientific support throughout the study lifecycle, ensuring protocol and regulatory compliance.
• Monitor study progress, participate in meetings, and support quality control of data.
• Review and interpret clinical trial data for decision-making and regulatory submissions.
• Partner with data management and biostatistics for data analysis and quality assurance.
• Assist in preparing study reports, publications, and scientific presentations.
• Serve as a scientific liaison between internal teams, CROs, and key stakeholders.
• Support communication of study progress and data to teams, leadership, and regulators.
• Contribute to regulatory submissions and ensure compliance with ethical and industry standards.

Qualifications:

• Advanced degree (PhD, PharmD, MD, or equivalent) in life sciences, pharmacy, or medicine.
• 3+ years of clinical research or development experience in biotech, pharma, or CRO settings.
• Strong knowledge of clinical study design, drug development, and regulatory requirements.
• Excellent analytical, communication, and teamwork skills.

This is a contract position