Sr. Medical Director, Clinical Research - Contract - Remote in US
Looking to escape your long commute to work? Unlock your new remote working position with this exciting role in clinical research!
Proclinical is seeking a Senior Medical Director to provide clinical leadership in the development of RNAi therapeutics, with a primary focus on neurodegenerative diseases.
Primary Responsibilities:
This role will involve driving clinical development programs, particularly for Huntington's Disease, while also contributing across other therapeutic areas as needed. You will collaborate with cross-functional teams and external experts to advance innovative treatments from early-phase research to regulatory approval.
Skills & Requirements:
- Medical degree (MD) with a strong research background; MD/PhD preferred.
- Expertise in neurology or neurodegenerative diseases, with experience in Huntington's Disease being advantageous.
- Proven track record in leading Phase 2-3 clinical programs, including interactions with health authorities.
- Strong understanding of clinical research, trial design, biostatistics, and regulatory guidelines.
- Exceptional written and verbal communication skills to present complex medical concepts effectively.
- Demonstrated problem-solving abilities and sound clinical judgment.
- Leadership experience in a matrixed environment, with a collaborative and entrepreneurial mindset.
- Familiarity with biotech-pharma partnerships is a plus.
The Sr Medical Director's responsibilities will be:
- Lead clinical development strategies and provide strategic direction for assigned programs.
- Develop and oversee clinical trial designs, ensuring global regulatory compliance.
- Monitor trial conduct and ensure patient safety throughout the study lifecycle.
- Collaborate with research teams to assess the feasibility of novel targets and design proof-of-concept studies.
- Work closely with cross-functional teams, including Regulatory, Biostatistics, Clinical Operations, Preclinical, and Commercial, to align development strategies.
- Prepare and review key deliverables such as regulatory submissions, protocols, informed consent forms, and scientific publications.
- Represent the organization at external meetings, including regulatory interactions and scientific conferences.
- Provide guidance on clinical decisions with significant strategic implications.
- Drive operational excellence and ensure adherence to timelines and deliverables.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Bo Forsen at b.forsen@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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