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Vice President Clinical Development

Avetix Group
Boston, MA Full Time
POSTED ON 2/6/2025
AVAILABLE BEFORE 5/2/2025

About the Company

We are seeking an experienced and visionary Vice President of Clinical Development (VP-CD) who can grow into or assume the role of Chief Medical Officer (CMO). This individual must possess a Medical Degree (MD) and have some experience in the muscle therapeutic area, including neuromuscular or musculoskeletal disorders. The ideal candidate will be a strategic thinker with a proven track record in clinical development and medical leadership, driving innovative therapies from early-phase development through to regulatory approval and commercialization.

About the Role

Design and Lead Clinical Programs : Develop and oversee clinical trial strategies, ensuring alignment with corporate objectives and regulatory requirements.

Protocol Development : Collaborate with cross-functional teams to create scientifically rigorous and innovative trial protocols.

Regulatory Engagement : Interface with regulatory authorities, including the FDA, EMA, and other global agencies, to secure trial approvals and navigate the regulatory landscape.

Data Analysis and Reporting : Oversee data interpretation, ensuring accurate and timely reporting to internal stakeholders, regulators, and the scientific community.

Responsibilities

  • Medical Leadership : Provide clinical and medical expertise across all stages of drug development, from preclinical transition to post-marketing.
  • Mentor and Guide Teams : Build and manage a high-performing clinical development team, fostering collaboration and innovation.
  • Cross-Functional Collaboration : Partner with research, regulatory, commercial, and market access teams to ensure the clinical program aligns with broader business goals.

Qualifications

  • Education : MD degree is mandatory. Additional training or certifications in clinical research, drug development, or neuromuscular / musculoskeletal medicine is highly desirable.
  • Experience : Minimum of 10 years of clinical development experience in the biopharmaceutical industry. Proven leadership in progressing therapies for muscle-related disorders through clinical development stages. Strong understanding of regulatory pathways, including IND, NDA, or BLA filings. Experience in interacting with regulatory agencies and KOLs.
  • Skills : Strategic thinking with a hands-on approach. Strong interpersonal and communication skills. Ability to analyze complex clinical data and present findings clearly.
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