Senior Clinical Research Director

Main Responsibilities:
- Develop and implement clinical development plan strategies.
- Lead, support, and oversee execution of clinical development and study activities.
- Collaborate across functions for a uniform, aligned operational approach; lead, build consensus, and coordinate action plans with other CRDs and stakeholders to resolve clinical study issues.
- Contribute to the clinical portion of submission dossiers, including regulatory and safety documents and meetings.
- Serve as the medical reference to ensure medical relevance of clinical data.
- Lead scientific data evaluation and dissemination.
- Ensure strict compliance with current regulations, laws and HA guidance, and with company policies and procedures.
- Foster a collaborative, engaging, high-performing environment for Clinical Research Directors and Clinical Scientists.

Minimum Requirements:
- Medical Doctor (MD) or equivalent with specialist training in Hematology, Internal Medicine, Pediatrics, or other relevant specialty.
- Minimum 8 years of experience.

Basic Qualifications / Skills:
- Strong scientific and clinical background with deep understanding of the therapeutic field.
- Expertise in clinical development and clinical study methodology.
- Understanding of pharmaceutical product development and lifecycle management.
- Excellent communication, problem-solving, and decision-making; ability to interact with cross-functional teams and key regulatory agencies.
- Strong leadership and collaboration; able to inspire and guide cross-functional teams.
- English fluent (spoken and written).

Preferred Qualifications:
- MD/PhD degree.

Benefits (explicitly stated):
- Wide range of health and wellbeing benefits, including at least 14 weeks’ gender-neutral parental leave.