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Clinical Research Scientist (Biotechnology, Remote)

Copenhagen, Capital Region
Posted 1 week, 1 day ago
Healthcare

About the role

Job summary

This role involves leading or co-leading clinical trials in alignment with global development strategies, collaborating with senior clinical staff to ensure high-quality and timely deliverables.

Responsibilities

  • Lead or co-lead less-complex clinical trials within a program.
  • Collaborate with a Medical Director and Senior Clinical Research Scientist on clinical trial activities.
  • Execute clinical trials in accordance with the clinical development plan (CDP).
  • Assist in developing trial protocols and regulatory documents.
  • Support the creation of electronic case report forms (eCRFs) and data management deliverables.
  • Contribute to the medical data review plan (MDRP) and summarize efficacy and safety data.
  • Participate in site selection and feasibility assessments, engaging with key opinion leaders (KOLs).
  • Assist in developing charters and coordinating committee meetings, including presentation preparation.
  • Liaise with project teams and contract research organizations (CROs) on study plans.
  • Prepare presentations for investigator meetings and training sessions as needed.

Qualifications

  • PhD, Pharm D, MS, or equivalent degree in medical, biological, pharmaceutical science, or related field.
  • Clinical research experience preferred; prior oncology/hematology drug development experience is a plus.
  • Ability to work in a project-oriented, matrixed team environment.
  • Excellent oral, written, and interpersonal communication skills.
  • Willingness to travel as necessary.

Skills

  • Passionate about the purpose of improving patient lives.
  • Precision and excellence in work.
  • Strong collaborative skills with diverse teams.
  • Innovative mindset and ability to handle uncertainty.
  • Experience in dynamic, fast-growing environments is desirable.

Education

  • Advanced degree (PhD, Pharm D, MS) in relevant fields.

Tools

  • Familiarity with clinical trial management systems and data analysis tools.
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