Senior / Principal Clinical Scientist, Clinical Development

Immunome$145K — $200K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD, MD, PharmD, MS, or equivalent degree in life sciences.
  • Minimum 2 years experience in clinical science or clinical development, preferably in oncology.
  • Strong leadership, project management, and communication skills.
  • Willingness to travel as necessary.

Responsibilities

  • Oversee clinical trial execution ensuring scientific and regulatory rigor.
  • Design and develop clinical trial protocols and informed consent forms.
  • Collaborate with investigators and trial sites for effective study execution.
  • Conduct data generation and validation tasks, including review and query resolution.
  • Prepare clinical study reports and regulatory submissions.
  • Review and develop training materials for site and CRA activities.
  • Engage in strategic development of clinical plans and timelines.
  • Present trial data to stakeholders, including scientific advisory boards.

Benefits

  • Opportunities for professional growth and advancement.
  • Access to cutting-edge research and development in oncology.
  • Supportive and collaborative team environment.
  • Involvement in impactful clinical trials that advance patient care.
Full Job Description
Position Overview

We are seeking a highly motivated and experienced Clinical Scientist to join our team. The Senior / Principal Clinical Scientist, Clinical Development will play a critical role in the design, execution, and interpretation of multiple 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 multiple clinical programs.

Responsibilities
  • Oversee the execution of clinical trials and ensure scientific and regulatory rigor.
  • Design and develop multiple 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 multiple trials.
  • Conduct activities related to data generation and validation, including CRF design and clinical data review/query resolution.
  • 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 strategic 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.
  • Mentor and develop junior team members with potential to manage direct reports.


Qualifications
  • PhD, MD, PharmD, MS, or equivalent degree in life sciences.
  • A minimum of 2 years of experience in clinical science, clinical research, or equivalent; clinical development experience is required, biopharmaceutical/biotechnology industry and oncology experience preferred.
  • Strong leadership, project management, and communication skills.
  • Travel may be required.


Knowledge and Skills
  • Extensive experience in drug development process, study design, clinical operations.
  • Extensive experience in clinical trial data analysis software and tools.
  • Strong 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.


WA State Range: Senior Clinical Scientist, Clinical Development - $145,823 - $182,019

WA State Range: Principal Clinical Scientist, Clinical Development - $169,883 - $200,742

Washington State Pay Range

$145,823-$200,742 USD

About Immunome

Immunome is a biotechnology company that develops next-generation cancer immunotherapies. The company's proprietary discovery engine identifies novel cancer targets and develops antibody-based therapies to treat cancer. Immunome's lead product candidate, IMM-BCP-01, is a first-in-class cancer immunotherapy that targets a novel cancer antigen. The company is headquartered in Philadelphia, Pennsylvania.
Learn more about Immunome
Size
20 employees
Market Cap
$33.6 million
Industry
NASDAQ

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