Senior Clinical Scientist Director, Endocrine & Rare Diseases

Ascendis Pharma; Hellerup; On-site; DKK 1,000,000 - 1,500,000; Full time

Benefits offered by this job

Office in Hellerup

Travel opportunities

Global collaboration

Job summary

Ascendis Pharma in Hellerup, Denmark, seeks a Senior Clinical Scientist to design, monitor and analyze clinical trials within the Endocrine & Rare Disease Medical Sciences organization. You will join a cross‑functional, global team and report to the VP of Clinical Science.

Based in Hellerup, you will participate in evening meetings due to time zone differences and may travel internationally. You will contribute to study design, data interpretation, regulatory submissions, and ongoing trial

Qualifications

• You hold a relevant degree, e.g., cand.pharm/Msc in Pharmacy or equivalent.
• You also have a strong track record of scientific and clinical inquiry.
• Understand statistical concepts and clinical trial design.

Responsibilities

• Design, provide oversight, and support site and subject retention in clinical trials.
• Ensure documents (protocols, brochures, monitoring plans, study reports, regulatory responses) are complete with cross‑functional teams.
• Participate in study teams and cross‑functional teams as appropriate and delegated.
• Maintain study integrity and track accumulating safety and efficacy data.
• Draft and review clinical documents, manuscripts, and regulatory submissions.
• Collaborate with cross‑functional colleagues to optimize product development.

Skills

Clinical trial design

Statistical concepts

Regulatory submissions

Data interpretation

Ethical judgment

Education

cand.pharm/MSc in Pharmacy

Job description

Ascendis Pharma in Hellerup, Denmark, seeks a Senior Clinical Scientist to design, monitor and analyze clinical trials within the Endocrine & Rare Disease Medical Sciences organization. You will join a cross‑functional, global team and report to the VP of Clinical Science.

Based in Hellerup, you will participate in evening meetings due to time zone differences and may travel internationally. You will contribute to study design, data interpretation, regulatory submissions, and ongoing trial