Job Description
Are you a visionary physician-scientist looking to bridge the gap between breakthrough laboratory science and life-saving patient therapies? Boston Advanced Therapeutics is seeking a high-caliber Medical Director of Clinical Research to lead our clinical development portfolio. In this pivotal role, you will champion the design, execution, and medical monitoring of phase I-III global oncology and immunology clinical trials.
We offer a highly collaborative, fast-paced environment where your medical expertise directly influences the pipeline of next-generation biologics. This is a premium opportunity to join an elite team of researchers, secure a highly competitive compensation package with equity, and drive therapies that will redefine patient care standards globally.
Responsibilities
- Provide strategic and medical leadership for global clinical trials, acting as the primary Medical Monitor to ensure patient safety and protocol adherence.
- Lead the design and optimization of clinical study protocols, investigator brochures, and regulatory submission documents (IND/NDA).
- Collaborate closely with clinical operations, biostatistics, and regulatory affairs teams to accelerate trial timelines and ensure data integrity.
- Foster strategic partnerships with key opinion leaders (KOLs), principal investigators, and clinical trial sites worldwide.
- Present scientific data and clinical progress at major international medical congresses and advisory boards.
- Oversee the analysis and interpretation of clinical trial data, driving the scientific publication strategy.
Qualifications
- Medical Doctor (MD or DO) degree with an active license and board certification/eligibility in Oncology, Immunology, or a related specialty.
- Minimum of 4-6 years of direct clinical research experience within the pharmaceutical, biotechnology, or CRO industry.
- Deep understanding of FDA, EMA, ICH-GCP guidelines, and the global drug development lifecycle.
- Proven track record of successful protocol design, clinical trial execution, and interaction with regulatory authorities.
- Exceptional leadership capabilities with a demonstrated ability to influence cross-functional matrix teams.
- Outstanding verbal and written communication skills, with a portfolio of peer-reviewed publications.