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Healthcare 🏢 Full Time ⭐️ Verified

Senior Clinical Scientist - Specialized Medicine

NovaCura Biomed
Cambridge, MA
Salary Estimate
USD 120.000 – USD 180.000
Posting Time
2 Mei 2026
Deadline
2 Mei 2027

Job description

Join NovaCura Biomed, a leader in Specialized Medicine, as a Senior Clinical Scientist based in Cambridge, MA. You will drive translational research and guide cross-functional teams to advance precision medicine therapies for patients with complex conditions.

In this pivotal role, you will partner with clinicians, biostatisticians, and regulatory specialists to design studies, interpret complex data, and communicate scientific insights to stakeholders and regulatory bodies.

We offer a collaborative environment, competitive compensation, and a path to leadership in a fast-growing field.

Responsibility

  • Lead end-to-end design, execution, and oversight of clinical research programs in targeted therapeutic areas within Specialized Medicine.
  • Collaborate with clinicians and scientists to translate preclinical findings into clinical study hypotheses and protocols.
  • Develop study protocols, case report forms, and statistical analysis plans; ensure regulatory compliance (ICH-GCP, FDA/EMA).
  • Coordinate cross-functional teams, manage timelines, budgets, and risk mitigation strategies.
  • Lead data management and advanced analyses (biostatistics, biomarker validation) to inform decision-making.
  • Prepare scientific publications, presentations, and regulatory submissions; support medical communications.
  • Mentor junior scientists and contribute to strategic direction for clinical development programs.

Qualification

  • MD or DO or PhD in Life Sciences (e.g., Medicine, Pharmacology, Biostatistics) with at least 5 years of clinical research experience.
  • Strong knowledge of regulatory guidelines (ICH-GCP, IND/CTA) and ethics in clinical trials.
  • Proven track record leading complex studies in specialized medicine, including rare diseases or precision therapies.
  • Expertise in study design, protocol development, and statistical analysis (R, SAS, Python).
  • Excellent scientific communication, grant/writing skills, and ability to present to diverse audiences.
  • Exceptional project management and cross-functional leadership; ability to work in a fast-paced, global environment.

Required Skills

Clinical Research Data Analysis Protocol Design Regulatory Compliance Biostatistics Medical Writing Cross-functional Leadership

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