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Associate Director, Biomarkers

GSK
Full-time
Remote friendly (Collegeville, PA)
United States
$144,750 - $241,250 USD yearly
Clinical Research and Development

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Role Summary

Associate Director, Biomarkers responsible for leading development of biomarker strategies for clinical trials, integrating biomarker approaches into clinical development plans, and serving as a biomarker lead on clinical matrix teams (CMT).

Responsibilities

  • Work with external industry and/or academic partners to evaluate, validate and establish biomarker capabilities and generate biomarker data to support strategies for clinical trial implementation.
  • Design, implement, and manage collaborative projects to develop biomarker capabilities of strategic importance to the program and in alignment with clinical trials.
  • Identify, develop, and implement advances in science and technology into biomarker strategies to guide indication selection, patient enrichment, and combination strategies.
  • Provide input to clinical biomarker teams on novel technologies enabling clinical development of candidate drugs.
  • Manage relationships with clinical biomarker leads, medical affairs, oncology teams, portfolio management, competitive intelligence, clinical development and management teams.
  • Contribute to and ensure quality of biomarker reports, summaries, data reviews and interpretations; present data at internal and external scientific forums; lead preparation/publication of manuscripts as needed.

Qualifications

  • Ph.D. in Biological Sciences or related field with 2+ years of experience, or
  • M.Sc with 5+ years of experience in biotechnology or pharmaceutical industry in biomarker applications in clinical trials.
  • Knowledge of biomarker assays, technologies and platforms and their application in clinical research.
  • Experience in biomarker discovery/development in a clinical setting.
  • Experience in matrixed, multidisciplinary team environments.
  • Demonstrated scientific expertise evidenced by publications, presentations, or internal/external reports.

Preferred Experience

  • Knowledge of GCP/GLP principles.
  • Strong prioritization, planning, and timely execution in fast-paced environments.
  • Strong interpersonal skills and ability to thrive in a matrix environment.
  • Dependable and trustworthy with ownership and responsibility.
  • Experience conducting biomarker analyses on various clinical sample types as part of a clinical study team.

Education

  • Not specified
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