Senior Clinical Research Scientist

Your Role:

As a Senior Clinical Research Scientist (CRS), you will serve as a subject matter expert and strategic partner to the Medical Lead, providing scientific, clinical, and operational input across early and late-stage clinical development programs. In this role, you will:

• Contribute to data interpretation, study designs, regulatory and study documents, and publication efforts
• Provide scientific input into pipeline programs
• Conduct Medical Monitoring and Medical Data Review activities in close collaboration with the Medical Lead, including oversight of Medical Monitoring activities performed by contracted vendors
• Engage and collaborate with a multi-disciplinary, global team, ensuring that scientific, clinical, and other relevant topics are appropriately considered in the context of highly complex data findings

Who You Are

You are an experienced clinical research professional with a strong scientific background and a passion for advancing innovative therapies. You bring:

Minimum Qualifications:

• Bachelor's and Master's Degree required
• Advanced degree in life sciences (e.g., PharmD, PhD, or MPH) and postdoctoral experience preferred
• Minimum of 3 years of experience in product and clinical development, with at least 5 years in a comparable role within the pharmaceutical, biopharmaceutical, or healthcare industry preferred

Preferred Qualifications:

• Proven track record of successfully leading or making significant contributions to clinical trials, with Phase III experience strongly preferred
• Educational and/or professional background in immunology is strongly desirable, with the ability to rapidly develop a working scientific knowledge across different therapeutic areas

Skills & Competencies:

• Ability to work both independently and collaboratively on tasks and projects of increasing complexity, with a commitment to scientific rigor
• Solid knowledge of regulatory requirements, including ICH-GCP guidelines
• Strong aptitude for interpreting and integrating complex data sets, including clinical safety and efficacy data, pharmacokinetics, biomarker data, and next-generation sequencing data
• High level of medical and clinical knowledge, with hands-on experience in clinical development and operations, including the ability to monitor laboratory and other clinical trial data
• Excellent communication and presentation skills, with the ability to contribute to abstracts and publications and to adapt messaging effectively for a variety of audiences