Clinical Scientist

Description

Job Title: Clinical Scientist

Company: Immunome, Inc.

Location: Bothell, WA, USA 

Company Overview

Immunome is a biotechnology company dedicated to developing first-in-class and best-in-class targeted cancer therapies. Our portfolio pursues each target with a modality appropriate to its biology, including immunotherapies, targeted effectors, radioligand therapies and antibody drug conjugates (ADCs). We believe that pursuing underexplored targets with appropriate drug modalities leads to transformative therapies. Our proprietary memory B cell hybridoma technology allows for the rapid screening and functional characterization of novel antibodies and targets. 

Position Overview

We are seeking a highly motivated and experienced Clinical Scientist to join our team. The Clinical Scientist will play a critical role in the design, execution, and interpretation of clinical trials for our oncology drug candidates. This individual will work closely with cross-functional teams, including clinical operations, regulatory affairs, and research and development, to ensure the successful progression of our clinical programs.

Responsibilities

• Design and develop clinical trial protocols, informed consent forms, and other study-related documents.
• Collaborate with principal investigators, key opinion leaders, and clinical trial sites to ensure robust study design and execution.
• Serve as Lead Clinical Scientist for one or more trials.
• Conduct activities related to data generation and validation, including CRF design and clinical data review/query resolution
• Ensure clinical trial data integrity and adherence to regulatory requirements.
• Contribute to the preparation of clinical study reports, regulatory submissions, and publications.
• Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities
• Perform site-facing activities such as training and responding to clinical questions
• Participate in the development of clinical development plans and timelines.
• Present clinical trial data and findings to internal and external stakeholders, including scientific advisory boards and regulatory agencies.

Requirements

Qualifications

• PhD, MD, PharmD, MS, or equivalent degree in life sciences
• Minimum of 3 years of experience in clinical science, clinical research, or equivalent; preferably in oncology.

Knowledge and Skills

• Proficiency in drug development process, study design, clinical operations
• Proficiency in clinical trial data analysis software and tools.
• Proficient knowledge and skills to support program specific data review, trend identification, and data interpretation
• Strong understanding of regulatory requirements and guidelines for clinical trials (e.g., GCP, ICH, FDA). 
• Excellent analytical, organizational, and communication skills.
• Ability to work effectively in a fast-paced, collaborative environment.
• Strong problem-solving skills and attention to detail.
• Travel may be required

E/E/O

Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. 

Salary band

$117,000 - $149,000