Senior Clinical Research Scientist

About the 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.

Responsibilities

• 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

Qualifications

• Minimum Qualifications
  • Master's Degree
  • 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 Qualifications
  • Advanced degree in life sciences (e.g., PharmD, PhD, or MPH) and postdoctoral experience preferred
  • 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

• 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

Location

Billerica, MA (3 days per week – Tuesday, Wednesday, Thursday)

Travel

Pay

$131,300.00 - $216,600.00 (base pay compensation)